| 小田 義直（おだ よしなお） | データ更新日：2024.04.16 |
教授 ／
医学研究院
基礎医学部門
病態制御学
| 1. | Murakami M, Hirahata K, Fujimori N, Yamamoto T, Oda Y, Kozono S, Ueda K, Ito T, Nakamura M, Ogawa Y. , Two cases of pancreatic neuroendocrine tumors with ectopic ACTH syndrome during their disease course., Clin J Gastroenterol. , doi: 10.1007/s12328-023-01908-5., 2024 Apr;17(2):363-370, 2024.04. |
| 2. | Ichiki T, Ito T, Oishi H, Kato K, Oda Y, Nakahara T. , Pigmented epithelioid melanocytoma arising from a teratoma of a Carney complex patient. , J Obstet Gynaecol Res. , doi: 10.1111/jog.15832., 2024 Feb;50(2):266-269, 2024.02. |
| 3. | Miyashita K, Kadota H, Hanada M, Inatomi Y, Oryoji C, Morishita A, Yoshida S, Oda Y, Kinoshita I. , Multiple lymphaticovenular anastomoses for chyluria in klippel-trenaunay syndrome. , Ann Plast Surg. , doi: 10.1097/SAP.0000000000003744., 2024 Feb;92(2):208-211, 2024.02. |
| 4. | Tocan V, Nakamura-Utsunomiya A, Sonoda Y, Matsuoka W, Mizuguchi S, Muto Y, Hijioka T, Nogami M, Sasaoka D, Nagamatsu F, Oba U, Kawakubo N, Hamada H, Mushimoto Y, Chong PF, Kaku N, Koga Y, Sakai Y, Oda Y, Tajiri T, Ohga S. , High-Titer Anti-ZSCAN1 antibodies in a toddler clinically diagnosed with apparent rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation syndrome., Int J Mol Sci. , doi: 10.3390/ijms25052820., 2024 Feb;25(5):2820, 2024.02. |
| 5. | Kawaguchi K, Endo M, Fukushima S, Hirose T, Nabeshima A, Fujiwara T, Oda Y, Nakashima Y. , Metastatic malignant glomus tumor resistant to pazopanib, a multikinase inhibitor: A case report and review of literature., JOS Case Reports., doi.org/10.1016/j.joscr., JOS Case Reports.2024, 2024.01. |
| 6. | Hayashida S, Ikenaga N, Nakata K, Nakamura S, Abe T, Ideno N, Endo M, Noguchi S, Oda Y, Nakamura M. , Repeated robotic pancreatectomy for recurrent pancreatic metastasis of mesenchymal chondrosarcoma: A case report., Asian J Endosc Surg. , doi: 10.1111/ases.13240., 2023 Oct;16(4):795-799, 2023.10. |
| 7. | Hongo T, Jiromaru R, Kuga R, Matsuo M, Oda Y, Nakagawa T. , Cholesterol granuloma of the anterior mediastinum: A case report and literature review., Int J Surg Case Rep., doi: 10.1016/j.ijscr.2023.108852., 2023 Oct:111:108852, 2023.10. |
| 8. | Hino Y, Kawakubo N, Takemoto J, Tamaki A, Kohashi K, Matsuura T, Oda Y, Tajiri T. , Hemorrhagic shock due to rupture of a nephroblastoma in an infant: A case report., JPS Case Reports., doi.org/10.1016/j.epsc.2023.102711, 2023 Oct;97:102711, 2023.10. |
| 9. | Ikeda S, Hu Q, Natsugoe K, Harima T, Tanaka Y, Kinoshita I, Nonaka K, Nambara S, Nakanishi R, Nakanoko T, Ota M, Kimura Y, Oki E, Oda Y, Yoshizumi T. , A pathological complete response after immunotherapy with pembrolizumab for distal duodenal adenocarcinoma caused by Lynch syndrome: a case report., Int Cancer Conf J. , doi: 10.1007/s13691-023-00622-w., 2023 Jul 26;12(4):279-284, 2023.07. |
| 10. | Imajo I, Yamada T, Chikui T, Kiyoshima T, Ito M, Kohashi K, Sakamoto E, Oda Y., Intraosseous synovial sarcoma of the mandible:a case report and review of the literature., Oncol Lett., doi: 10.3892/ol.2023.13904, 2023 Jun;26(1):318, 2023.06. |
| 11. | Yoshimoto M, Setsu N, Yokoyama N, Taguchi K, Kohashi K, Oda Y. , Secondary Peripheral Dedifferentiated Chondrosarcoma: A Case Report with Special Emphasis on the Radiology/Pathology Correlation. , JBJS Case Connect. , doi: 10.2106/JBJS.CC.21.00783., 2023 Jun;13(2), 2023.06. |
| 12. | Wakasugi A, Kimura Y, Natsugoe K, Nakanoko T, Nonaka K, Nambara S, Hu Q, Nakanishi R, Ota M, Oki E, Oda Y, Yoshizumi T. , Combined treatment with surgery and immune checkpoint inhibitor extended survival in a case of gastric intramural metastasis from esophageal cancer: a case report., Surg Case Rep., doi: 10.1186/s40792-023-01703-x., 2023 Jun;9(1):118, 2023.06. |
| 13. | 山元英崇、大久保文彦、山口知彦、堀田多恵子、古賀裕、小田義直 , 病理検査室のマネジメント総論, 病理と臨床., 2023 Jun;41(6):562-567, 2023.06. |
| 14. | Higuchi N, Honda Y, Koga Y, Asai H, Ono H, Kato W, Nakashima K, Cuesta E, Tsujino T, Yamamoto H, Kusuhara K, Hisaoka M, Ohga S., TRK-inhibitor control of an NTRK-rearranged spindle cell tumor with malignant transformation in an adolescent.（Online ahead of print.）, Pediatr Blood Cancer., doi: 10.1002/pbc.30379., 2023 May;e30379, 2023.05. |
| 15. | Goto H, Koga Y, Kohashi K, Ono H, Takemoto J, Matsuura T, Tajiri T, Ihara K, Oda Y, Ohga S., Pancreatoblastoma with a novel fusion gene of IQSEC1-RAF1., Pediatr Blood Cancer. , doi: 10.1002/pbc.30155., 2023 Apr;70(4):e30155, 2023.04. |
| 16. | 木下伊寿美、小田義直
, 骨・軟部 横紋筋肉腫（胎児型、胞巣型）, 病理と臨床., 2023 Apr;41(臨時増刊号):273, 2023.04. |
| 17. | 木下伊寿美、小田義直, 骨・軟部 粘液線維肉腫, 病理と臨床., 2023 Apr;41(臨時増刊号):273, 2023.04. |
| 18. | Kono J, Yoshimaru K, Matsuura T, Tamaki A, Takemoto J, Matsumoto S, Hotta T, Kohashi K, Oda Y, Tajiri T. , COVID19 detection in appendix of acute appendicitis in a child: a case report and review of literature., Surg Case Rep. , doi: 10.1186/s40792-023-01618-7., 2023 Mar 14;9(1):37, 2023.03. |
| 19. | Sugimoto R, Uesugi N, Yamada N, Osakabe M, Baba S, Yanagawa N, Akiyama Y, Habano W, Sasaki A, Oda Y, Sugai T., Gastroblastoma mimics the embryonic mesenchyme of the foregut: a case report., Diagnostic Pathology., 2023;(18)24, 2023.02. |
| 20. | Hornick JL, Webster F, Dei Tos AP, Hemmings C, Miettinen M, Oda Y, Raut CP, Rubin BP, Von Mehren M, Wardelmann E, Fletcher CDM. , Dataset for reporting of gastrointestinal stromal tumours: recommendations from the International Collaboration on Cancer Reporting (ICCR)., Histopathology. , doi: 10.1111/his.14791., 2023 Feb;82(3):376-384, 2023.02. |
| 21. | Morii E, Hatanaka Y, Motoi N, Kawahara A, Hamakawa S, Kuwata T, Nagatomo T, Oda Y, Okamoto A, Tanaka R, Iyoda A, Ichiro M, Matsuo Y, Nakamura N, Nakai T, Fukuhara M, Tokita K, Yamaguchi T, Takenaka M, Kawabata A, Hatanaka KC, Tsubame K, Satoh Y; Working Group on Cytology in the Era of Genomic Medicine., Guidelines for handling of cytological specimens in cancer genomic medicine.（Online ahead of print.）, Pathobiology., doi: 10.1159/000528346., 2023 Feb;1-23, 2023.02. |
| 22. | Kaitsumaru M, Shiota M, Takamatsu D, Blas L, Matsumoto T, Inokuchi J, Oda Y, Eto M. , Interstitial pneumonia after regression by olaparib for neuroendocrine prostate cancer with BRCA1 mutation: a case report. , Int Cancer Conf J., doi: 10.1007/s13691-022-00592-5., 2023 Jan 3;12(2):131-136, 2023.01. |
| 23. | 半田瑞樹、藤田綾、中島豊、小島雅之、亀井敏昭、小田義直、西山憲一 , 嚢胞形成を伴う縦隔中皮腫の1例, 診断病理, 2023 Jan;40(1)55-59, 2023.01. |
| 24. | Tanabe M, Yoshikawa H, Yamada Y, Oda Y, Sonoda KH. , A case of primary orbital solitary fibrous tumor with lung metastases 41 years after initial treatment., Orbit., doi: 10.1080/01676830.2021.1954665., 2022 Dec;41(6):810-814, 2022.12. |
| 25. | Tomiyama T, Itoh S, Toshida K, Morinaga A, Fujimoto-Kosai Y, Tomino T, Kurihara T, Nagao Y, Morita K, Harada N, Kohashi K, Eguchi Y, Oda Y, Mori M, Yoshizumi T., A rare case of unresectable, microsatellite instability-high hepatocellular carcinoma and an examination of the tumor microenvironment., Int Cancer Conf J., doi: 10.1007/s13691-022-00585-4, 2022 Nov;12(1):81-86, 2022.11. |
| 26. | 小田義直 , 2020年骨・軟部腫瘍WHO分類における新疾患概念, 日本整形外科学会雑誌, 2022 Oct;96(10):878-886, 2022.10. |
| 27. | 髙橋俊介、岩尾梨沙、荒殿ちほ子、橋本憲和、今村壮志、本間仁、桑野博行、梅北慎也、佐々木泰介、小田義直 , 潰瘍を形成した胃hamartomatous inverted polypの1例, 日本消化器内視鏡学会雑誌. , 2022 Oct;64(10)2268-2274, 2022.10. |
| 28. | 遠峰由希恵、大久保文彦、山元英崇、山口知彦、野上美和子、中附加奈子、仲正喜、小田義直 , 病理検体を用いた遺伝子検査における作業効率化・標準化のための取り組み－チェックシートによる情報管理の有用性－, 医学検査., doi:10.14932/jamt.22-15, 2022 May;71(3):528-537, 2022.08. |
| 29. | Takeda A, Sakoda T, Yawata N, Kato K, Hasegawa E, Shima T, Hikita S, Yoshitomi K, Takenaka K, Oda Y, Akashi K, Sonoda KH. , Panuveitis induced by donor-derived CD8 + T cells after allogeneic hematopoietic stem cell transplantation for adult T-cell leukemia. , Am J Ophthalmol Case Rep., doi: 10.1016/j.ajoc.2022.101673., 2022 Aug;27:101673, 2022.08. |
| 30. | Hatae R, Mizoguchi M, Arimura K, Kiyozawa D, Shimogawa T, Sangatsuda Y, Nishimura A, Ono K, Oda Y, Yoshimoto K. , Giant cranial angiolipoma with arteriovenous fistula: a case report., Surg Neurol Int., doi: 10.25259/SNI_422_2022, 2022 Jul;13:314, 2022.07. |
| 31. | Tada Y, Yasunaga M, Tomonobe H, Yamada Y, Hori E, Okugawa K, Yahata H, Oda Y, Kato K., A Case of Malignant Phyllodes Tumor of the Breast Metastasizing to the Ovary., Int J Surg Pathol., doi: 10.1177/10668969211056912., 2022 Jun;30(4):427-431, 2022.06. |
| 32. | Ono Y, Toyokawa G, Tagawa T, Ijichi K, Oda Y, Mori M. , IgG4-related lung disease exhibiting the invasion into the diaphragm: a case report. , Ann Thorac Cardiovasc Surg., doi: 10.5761/atcs.cr.19-00244, 2022 Jun 20;28(3):223-226, 2022.06. |
| 33. | Toda Y, Morimoto T, Matsumoto Y, Setsu N, Yoshihara T, Aishima S, Oda Y, Nakashima Y, Mawatari M., Application of contralateral osteotomy for the en bloc resection of paraspinal and spinal tumours: a report of three cases.( Online ahead of print ), Br J Neurosurg., doi: 10.1080/02688697.2022.2076809., 2022 May;1-7, 2022.05. |
| 34. | Tsuchihashi K, Yamaguchi K, Taguchi R, Kohashi K, Ijichi K, Okumura Y, Nakano M, Ohno A, Hioki T, Shimokawa H, Ariyama H, Kusaba H, Oda Y, Akashi K, Baba E. , Spontaneous regression of metachronous intra-abdominal desmoid tumor in a patient with familial adenomatous polyposis. , Case Rep Oncol. , https://doi.org/10.1159/000521920, 2022;15:71-77, 2022.04. |
| 35. | 藤原美奈子、川床慎一郎、井星陽一郎、隅田頼信、吉村大輔、原田直彦、小田義直, 予後不良な早期消化管癌の病理組織学的特徴 食道癌 , 胃と腸, 2022 Apr 57(4):355-363, 2022.04. |
| 36. | 岩崎健、山元範昭、小田義直
, がんの分子病理学（各論）臓器がん 骨軟部腫瘍 , 病理と臨床. , 2022 Apr;40(臨時増刊号):317-324, 2022.04. |
| 37. | Oketani H, Onaka S, Handa M, Oda Y, Nakamura T. , Solitary fibrous tumor of the pineal region in the elderly: a case report. , Int J Surg Case Rep., doi: 10.1016/j.ijscr.2022.106802., 2022;91:106802, 2022.01. |
| 38. | 阿部千恵、米田玲子、毛利太郎、山田優衣、山田裕一、小田義直
, 下行結腸原発Histiocytic sarcomaの1例, 診断病理, 2022 Jan;39(1)56-61 , 2022.01. |
| 39. | Oba U, Koga Y, Hata N, Oda Y, Ohga S., Nivolumab therapy for a pediatric-onset primary intracranial melanoma. , Pediatr Int. , doi: 10.1111/ped.14956., 2022 Jan;64(1):e14956, 2022.01. |
| 40. | 合島怜央奈、森啓輔、檀上敦、大石光寿、江頭玲子、山田裕一、入江裕之、小田義直、相島慎一、山下佳雄 , 外傷を契機に発見された頬部悪性末梢神経鞘腫瘍の１例, 頭頸部癌, 2021 Dec;47(4):388-394, 2021.12. |
| 41. | Kawasaki J, Toshima T, Yoshizumi T, Itoh S, Mano Y, Wang H, Iseda N, Harada N, Oda Y, Mori M. , ASO visual abstract: Prognostic impact of Vessels that Encapsulate Tumor Cluster (VETC) in patients who underwent liver transplantation for hepatocellular carcinoma. , Ann Surg Oncol., doi: 10.1245/s10434-021-10248-y., 2021 Dec;28(Suppl 3):512-513, 2021.12. |
| 42. | Toda Y, Yamada Y, Kohashi K, Ishihara S, Ito Y, Susuki Y, Kawaguchi K, Kinoshita I, Kiyozawa D, Mori T, Kuboyama Y, Tateishi Y, Yamamoto H, Fujiwara T, Setsu N, Endo M, Matsumoto Y, Nakashima Y, Mawatari M, Oda Y. , Prognostic implication of desmoplastic stroma in synovial sarcoma: a histological review., Pathol Res Pract., doi: 10.1016/j.prp.2021.153668., 2021 Dec;228:153668, 2021.12. |
| 43. | Miyama A, Kuratsu S, Takenaka S, Yoshimura M, Yoneda G, Yamada Y, Oda Y. , Two case reports of intra-articular nodular fasciitis of the knee confirmed by MYH9-USP6 gene fusion expression. , J Orthop Sci., doi: 10.1016/j.jos.2018.12.008., 2021 Nov;26(6):1138-1142, 2021.11. |
| 44. | Tada Y, Yasunaga M, Tomonobe H, Yamada Y, Hori E, Okugawa K, Yahata H, Oda Y, Kato K. （Online ahead of print.）, A Case of Malignant Phyllodes Tumor of the Breast Metastasizing to the Ovary., Int J Surg Pathol., doi: 10.1177/10668969211056912., 2021 Nov;10668969211056912, 2021.11. |
| 45. | 木下伊寿美、孝橋賢一、小田義直
, 【第62回日本小児血液・がん学会学術集会】シンポジウム5：小児がんの中央病理診断－次世代へつなぐために 希少がんの病理診断支援体制―骨軟部腫瘍をモデルに, 日本小児血液・がん学会雑誌., 2021 Nov;58(3):215-217, 2021.11. |
| 46. | Yamamoto H, Kusafuka K, Nozaki Y, Iwasaki T, Nogami M, Hongo T, Yasumatsu R, Oda Y. , Carcinoma showing thymus-like differentiation (CASTLE) of the salivary gland: Report of 2 cases of a hitherto under-recognized extrathyroid counterpart. Online ahead of print., Pathol Res Pract. , doi: 10.1016/j.prp.2021.153646. , 2021 Oct;227:153646, 2021.10. |
| 47. | Omori A, Yoshimaru K, Souzaki R, Nakamura M, Kaku N, Koga Y, Shibui Y, Tamaki A, Takemoto J, Kawakubo N, Kohashi K, Ohga S, Oda Y, Matsuura T. , Successful management of Wilms tumor accompanied by traumatic renal injury: a case report. , Int Cancer Conf J., doi: 10.1007/s13691-021-00496-w., 2021 Jun;10(4):300-304, 2021.10. |
| 48. | 藤本翔大、浅川拓也、小嶋健太、山本将義、野中修一、藤田綾、田口健一、横山良平、孝橋賢一、小田義直 , 骨巨細胞腫との鑑別が困難であった非骨化性線維腫の1例 , 日本臨床細胞学会九州連合会雑誌. , 2021;52:29-34, 2021.10. |
| 49. | 渡邊壽美子、加来恒壽、西村和徳、植村瑞紀、上原俊貴、杉島節夫、加藤聖子、小田義直、岩坂剛 , 子宮頸部腺系病変における細胞像の数量的解析 －AGC に注目して－ , 日本臨床細胞学会九州連合会雑誌. , 2021;52:11-17, 2021.10. |
| 50. | 小田義直 , 骨・軟部腫瘍病理診断のポイント , 日本整形外科学会雑誌. , 2021 Oct;95(10):848-856, 2021.10. |
| 51. | Ishihara S, Kohashi K, Kuboyama Y, Nakashima Y, Oda Y., Parosteal osteosarcoma with a manifestation of subperiosteal low-grade central osteosarcoma., Skeletal Radiol., doi: 10.1007/s00256-021-03747-2., 2021 Sep;50(9):1903-1907, 2021.09. |
| 52. | Ide F, Ito Y, Kikuchi K, Satomura K, Ogawa I, Yamamoto H. , Activating HRAS mutation in a case of inverted ductal papilloma of the salivary gland. Online ahead of print., Pathol Int. 2021 Sep, doi: 10.1111/pin.13166. , 2021.09. |
| 53. | 遠藤和也、池田真一郎、園田裕樹、山口方規、富川盛雅、池田泰治、東秀史、竹中賢治、藤原美奈子、小田義直、陣内重三 , 結腸穿孔による急性腹膜炎を合併し、大腸癌との鑑別が困難であった硬化性腸間膜炎の1例, 臨床と研究. , 2021 Sep;98(9):1115-1118, 2021.09. |
| 54. | Matsuura T, Kohashi K, Kawano Y, Takahashi Y, Yoshimaru K, Yoshizumi T, Oda Y, Mori M, Taguchi T., Successful management to prevent early graft loss due to Seventh-day Syndrome after liver retransplantation: A case report and literature review., Pediatr Transplant., doi: 10.1111/petr.13907., 2021 Aug;25(5):e13907, 2021.08. |
| 55. | Tanabe M, Yoshikawa H, Yamada Y, Oda Y, Sonoda KH.
, A case of primary orbital solitary fibrous tumor with lung metastases 41 years after initial treatment. Online ahead of print. , Orbit. , doi: 10.1080/01676830.2021.1954665. , 2021 Jul;1-5, 2021.07. |
| 56. | Takagi K, Kikuchi K, Hiwatashi A, Togao O, Sangatsuda Y, Kuga D, Mizoguchi M, Yamamoto H, Iwaki T, Ishigami K. , Papillary craniopharyngioma coexisting with an intratumoral abscess in a pediatric patient: A case report and review of the literature. , Acta Radiol Open., doi: 10.1177/20584601211030661, 2021 Jul;10(7):20584601211030661, 2021.07. |
| 57. | Yanagihara T, Matsumoto K, Yoneda R, Egashira A, Mannoji H, Watanabe H, Hanaoka K, Nakayama Y, Ogo N, Inutsuka Y, Asoh T, Kohashi K, Kinoshita I, Oda Y, Maeyama T. , Lenvatinib for poorly differentiated carcinoma of the anterior mediastinum. , Respir Med Case Rep. , doi: 10.1016/j.rmcr.2021.101477., 2021 Jul;33:101477, 2021.07. |
| 58. | Tsubouchi K, Ibusuki R, Makisumi K, Okamoto H, Iwasaki T, Okamatsu Y, Inoue K, Harada T. , Tumor embolism as a cause of renal artery occlusion and acute kidney injury diagnosed and treated with endovascular intervention in a patient with mediastinal undifferentiated sarcoma., Intern Med. , doi: 10.2169/internalmedicine.6249-20., 2021 Jun;60(12):1907-1910, 2021.06. |
| 59. | Hashimoto H, Ito T, Yamada Y, Oda Y, Furue M., Onychopapilloma presenting as longitudinal melanonychia: A case report and literature review., Australas J Dermatol., doi: 10.1111/ajd.13543., 2021 May;62(2):244-246, 2021.05. |
| 60. | 宮﨑佳子、山田裕一、小田義直, 久山町研究60年のあゆみ～最新知見と将来展望～病理学分野 , メディカル・ビューポイント., 2021 May;42(5):5-6, 2021.05. |
| 61. | 家村綾子、柳町昌克、田崎彰久、廣田由佳、大西威一郎、神谷尚宏、津島文彦、原田浩之、木下伊寿美、孝橋賢一、小田義直、高木正稔、明石巧、朝蔭孝宏、森尾友宏 , 出生時から開口障害を認めたデスモイド型線維腫症, 日本小児科学会雑誌 , 2021 Apr;125(4):619-624, 2021.04. |
| 62. | 戸田雄、小田義直, 骨 治療方針を変える病理所見 診療ガイドラインと治療戦略 , 病理と臨床. , 2021 Apr;39(臨時増刊号):169-175, 2021.04. |
| 63. | Nagano T, Itoh S, Miyashita Y, Shimagaki T, Wang H, Kurihara T, Nagao Y, Toshima T, Harada N, Kohashi K, Ogata Y, Oki E, Oda Y, Yoshizumi T, Mori M. , Late recurrence of cancer stem cell-positive colorectal cancer liver metastases after 15 years., Clin J Gastroenterol., doi: 10.1007/s12328-020-01330-1., 2021 Apr;14(2):613-616, 2021.04. |
| 64. | 小田義直 , SWI/SNF複合体発現欠失腫瘍, 病理と臨床. , 2021 Apr;39(5):506-509, 2021.04. |
| 65. | *Tahara M, Fujino Y, Yamasaki K, Oda K, Kido T, Sakamoto N, Kawanami T, Kataoka K, Egashira R, Hashisako M, Suzuki Y, Fujisawa T, Mukae H, Suda T, Yatera K. , Exposure to PM 2.5 is a risk factor for acute exacerbation of surgically diagnosed idiopathic pulmonary fibrosis: a case-control study., Respir Res. , doi: 10.1186/s12931-021-01671-6., 2021 Mar;22(1):80, 2021.03. |
| 66. | 島田有貴、水内祐介、目井孝典、佐田政史、永吉絹、永井俊太郎、山田裕、古賀裕、小田義直、中村雅史 , 膵移植後に生じた低異型度虫垂粘液性腫瘍の 1 切除例, 日本大腸肛門病会誌, 2021 Mar;74(3):184-189, 2021.03. |
| 67. | Akaki M, Ishihara A, Nagai K, Naono H, Taguchi K, Yamamoto H, Tanaka H, Kataoka H. , Signet ring cell differentiation in salivary duct carcinoma with rhabdoid features: Report of three cases and literature review. , Head Neck Pathol. , doi: 10.1007/s12105-020-01186-4., 2021 Mar;15(1):341-351, 2021.03. |
| 68. | Toda Y, Matsumoto Y, Morimoto T, Mawatari M, Oda Y, Nakashima Y., En bloc resection for a malignant spine tumor after balloon kyphoplasty: Histological findings of a retrieved vertebral body: A case report., JBJS Case Connect., doi: 10.2106/JBJS.CC.20.00114., 11(1), 2021.02. |
| 69. | Hashimoto H, Ito T, Yamada Y, Oda Y, Furue M. , Eosinophilic infiltration discriminates lichen-planus-like eruption caused by an immune checkpoint inhibitor from ordinary lichen planus. , J Dermatol., doi: 10.1111/1346-8138.15705., 48(2):e102-103, 2021.02. |
| 70. | Ohno A, Fujimori N, Miki M, Oono T, Igarashi H, Matsuda R, Koga Y, Oda Y, Ohtsuka T, Nakamura M, Ito T, Ogawa Y. , Collision of a pancreatic ductal adenocarcinoma and a pancreatic neuroendocrine tumor associated with multiple endocrine neoplasm type 1. , Clin J Gastroenterol. , doi: 10.1007/s12328-020-01234-0., 2021 Feb;14(1):358-363, 2021.02. |
| 71. | 原田昇、吉住朋晴、孝橋賢一、小田義直、森正樹, 肝孤立性線維性腫瘍 肝・胆道系症候群Ⅱ －その他の肝・胆道系疾患を含めて－ , 日本臨牀. 2021 Feb;:246-248, 2021.02. |
| 72. | Kuboyama Y, Yamada Y, Kohashi K, Toda Y, Kawakami K, Kitahara D, Nishiyama K, Hiraki Y, Oya M, Oda Y., Three cases of synovial sarcoma of gastric wall: A case report and review of the literature., Pathol Res Pract., doi: 10.1016/j.prp.2021.153352. , 2021 Jan;219:153352 , 2021.01. |
| 73. | Wang H, Itoh S, Matsumoto Y, Nishie A, Kurihara T, Shimagaki T, Nagao Y, Toshima T, Harada N, Kohashi K, Oda Y, Ishigami K, Maruyama H, Yoshizumi T, Mori M., Surgically resected hepatic mass caused by fascioliasis., Clin J Gastroenterol., doi: 10.1007/s12328-021-01339-0. Online ahead of print., 2021.01. |
| 74. | Itoh S, Yugawa K, Yoshizumi T, Oda Y, Mori M. , Editorial: Immune microenvironment in primary and metastatic liver cancers., Hepatol Res., doi: 10.1111/hepr.13607., 51(1):3-4, 2021.01. |
| 75. | Kobayashi H, Kobayashi S, Shiota M, Takamatsu D, Abe T, Kashiwagi E, Takeuchi A, Inokuchi J, Kohashi K, Shioyama Y, Oda Y, Eto M. , Salvage robot-assisted radical prostatectomy after carbon ion radiotherapy: a case report., Int Cancer Conf J. , doi: 10.1007/s13691-020-00464-w. , 2021 Jan;10(2):96-99, 2021.01. |
| 76. | Yoshimaru K, Taguchi T, Fujiyoshi T, Kono T, Aung NNT, Than MT, Oo YM, Oo T, Kakazu M, Miyazaki K, Shibui Y, Takahashi Y, Kohashi K, Shwe EE, Tsuchihashi K, Endo M, Matsuura T, Oda Y, Aye Aye, Yoshioka H, Yoshioka H.
, Surgical extirpation of a huge desmoid fibromatosis of the right buttock: Case report of a successful international collaboration. , SN Compr. Clin. Med. , doi.org/10.1007/s42399-021-00860-0, 2021, 2021.01. |
| 77. | 小田義直、牛久哲男、羽賀博典、谷田部恭、山元英崇, 円滑な“がんゲノム医療遂行”のための病理医の役割 , Histo-Logic Japan., 2021 49:(1)2-9, 2021.01. |
| 78. | Harada Y, Kubo M, Kai M, Yamada M, Zaguirre K, Ohgami T, Yahata H, Ohishi Y, Yamamoto H,Oda Y, Nakamura M. , Breast metastasis from pelvic high-grade serous adenocarcinoma: a report of two cases. , Surg Case Rep., 6(1):317, 2020.12. |
| 79. | Shindo K, Ohuchida K, Moriyama T, Kinoshita F, Koga Y, Oda Y, Eto M, Nakamura M. , A rare case of PSA-negative metastasized prostate cancer to the stomach with serum CEA and CA19-9 elevation: a case report., Surg Case Rep. , 6(1):303, 2020.12. |
| 80. | 小田義直 , 速報解説！ここが変わった「WHO Classification of Tumours・5th Edition, Soft Tissue and Bone Tumours」改訂ポイント, 病理と臨床., 38(12)1139-1141, 2020.12. |
| 81. | Imajima T, Ito M, Shinohara Y, Tsuchihashi K, Ariyama H, Kusaba H, Yamamoto H, Oda Y, Akashi K, Baba E. , Favorable response to combined androgen blockade for metastatic cutaneous apocrine carcinoma: a case report., IJS Oncology. , 2020 Dec;5(6):e105, 2020.12. |
| 82. | Yoshimaru K, Matsuura T, Yanagi Y, Takahashi Y, Kohashi K, Kaku N, Oda Y, Ohga S, Taguchi T. , Successful urgent living donor liver transplantation for massive liver necrosis accompanied by nonocclusive mesenteric ischemia in a biliary atresia infant: A case report., Transplant Proc. , doi: 10.1016/j.transproceed.2020.06.010. , 2020 Nov;52(9):2802-2808 , 2020.11. |
| 83. | Yada Y, Koga Y, Ono H, Motomura Y, Esumi G, Kohashi K, Muraosa Y, Kamei K, Matsuura T, Oda Y, Ohga S., Acute isolated aspergillus appendicitis in pediatric leukemia. , J Infect Chemother. , 2020 Nov;26(11):1229-1231, 2020.11. |
| 84. | Toyota S, Nakanishi R, Miyashita Y, Yoshino S, Fujimoto Y, Jogo T, Hu Q, Hokonohara K,Hisamatsu Y, Ando K, Kimura Y, Oki E, Oda Y, Mori M. , Quadruple gastrointestinal cancer with discordance of mismatch repair protein deficiency and microsatellite instability suggesting lynch syndrome. , Int Cancer Conf J. , 10(1):2-5, 2020.11. |
| 85. | 久保山雄介、山田裕一、小田義直、平岡伸介 , 希少がんの病理診断 コンサルテーション体制について, 腫瘍内科. 2020 Oct;26(4):425-431, 2020.10. |
| 86. | 戸田雄、小田義直 , 肉腫の病理診断 WHO診断基準（2020）, 日本臨床, 2020 Oct;78増刊号(5):168-182, 2020.10. |
| 87. | 中附加奈子、大久保文彦、内龍太郎、野﨑優衣、山元英崇、小田義直, 穿刺吸引細胞診で悪性を疑った慢性甲状腺炎の一例, 日本臨床細胞学会九州連合会雑誌, 2020 Oct;51:63-67, 2020.10. |
| 88. | 藤本翔大、桑田理左、小嶋健太、野中修一、北里謙二、杉井梓、奥村幸彦、瀧澤克実、田口健一、小田義直, 粘液型脂肪肉腫9例の細胞学的検討, 日本臨床細胞学会九州連合会雑誌, 2020 Oct;51:35-40, 2020.10. |
| 89. | Ono Y, Takada K, Osoegawa A, Kinoshita F, Oba T, Tsukamoto S, Tagawa T, Oda Y, Mori M. , First-line osimertinib for leptomeningeal metastasis from lung adenocarcinoma with EGFR mutation as the initial and solitary site of postoperative recurrence. , Int Cancer Conf J. , 10(1):78-82, 2020.10. |
| 90. | Hashizume N, Aiko T, Fukahori S, Ishii S, Saikusa N, Koga Y, Higashidate N, Sakamoto S, Tsuruhisa S, Nakahara H, Muta H, Miyoshi H, Naito Y, Yamamoto H, Oda Y, Tanaka Y, Yagi M. , Benign mesenteric lipomatous tumor in a child: a case report and literature review. , Surg Case Rep. , doi: 10.1186/s40792-020-01020-7., 2020 Sep;6(1):243 , 2020.09. |
| 91. | Hasuda H, Hu Q, Miyashita Y, Zaitsu Y, Tsuda Y, Hisamatsu Y, Nakashima Y, Ando K, Kimura Y, Yamada Y, Oki E, Oda Y, Mori M. , Gastric glomus tumor with a preoperative diagnosis by endoscopic ultrasonography-guided fine needle aspiration: a case report. , Int Cancer Conf J. , 10(1):35-40, 2020.09. |
| 92. | 下川雄三、宮ヶ原典、寺松克人、末廣侑大、久野敏、植田圭二郎、山本一郎、山田裕一、小田義直、麻生暁、藤森尚、大野隆真 , 膵癌に対するgemcitabine投与中に発症した血栓性微小血管障害を早期に診断し得た2症例, 膵臓. , 35(5):403-411, 2020.09. |
| 93. | Kuriyama N, Ando K, Hu Q, Miyashita Y, Fujimoto Y, Jogo T, Hokonohara K, Nakanishi R,Hisamatsu Y, Kimura Y, Tsurumaru D, Kohashi K, Oda Y, Oki E, Nishimura M, Mori M. , Obstructive rectal endometriosis treated by robot-assisted laparoscopic surgery: a case report., Surg Case Rep. , doi: 10.1186/s40792-020-00977-9., 2020 Aug;6(1):211 , 2020.08. |
| 94. | Ogata H, Harada E, Moriya S, Fukuyama S, Suzuki K, Shiraishi Y, Ando H, Uryu K, Shinozaki S, Ide M, Sakamoto A, Nakanishi T, Hamada N, Yoneshima Y, Ota K, Kohashi K, Tateishi Y, Miyashita Y, Oda Y, Matsumoto K., Pleuropulmonary paragonimiasis with multiple nodules in the pleura., Intern Med., doi: 10.2169/internalmedicine.4457-20., 2020 Aug;59(15):1879-1881, 2020.08. |
| 95. | 玉城昭彦、吉丸耕一朗、入江敬子、孝橋賢一、田口智章、小田義直 , Hirschsprung病およびHirschsprung病類縁疾患の病理と臨床 特集：小児非腫瘍性疾患の病理と臨床, 病理と臨床., 38(8):677-686, 2020.08. |
| 96. | Toyota S, Kimura Y, Fujimoto Y, Jogo T, Hu Q, Hokonohara K, Nakanishi R, Hisamatsu Y, Ando K,Oki E, Oda Y, Miyashita Y, Kohashi K, Mori M. , A rare case of esophageal adenocarcinoma with urinary bladder metastasis., Int Cancer Conf J., 9(4):231-234, 2020.07. |
| 97. | 立石悠基、小田義直 , ゲノム診療用病理組織検体取扱い規程, 検査と技術, 2020 Jun;48(6):575-577, 2020.06. |
| 98. | 遠藤誠、戸田雄、小田義直、中島康晴、松本嘉寛
, 骨・軟部腫瘍 専門医試験をめざす症例問題トレーニング, 整形外科, 2020 Jun;71(7):811-816, 2020.06. |
| 99. | Kyohei Yugawa, Kenichi Kohashi, Shinji Itoh, Tomoharu Yoshizumi, Ichiro Sakamoto, Hiroyuki Tsutsui, Masaki Mori, Yoshinao Oda, Combined hepatocellular-cholangiocarcinoma after tetralogy of Fallot repair a case report and review of literature, Pathology Research and Practice, 10.1016/j.prp.2020.152908, 2020.05, [URL], Background: Liver fibrosis and cancer are serious hepatic complications for patients with congenital heart diseases. We present a rare case of combined hepatocellular carcinoma (HCC) and cholangiocarcinoma (CCA) (cHCC-CCA) after the repair of tetralogy of Fallot (TOF). Case presentation: A 54-year-old Japanese woman had undergone biventricular repair for TOF at 7 years old. She presented with abdominal distension. Abdominal CT revealed ascites and a 90-mm tumor involving the liver's left lobe. Tumor marker values were: alpha-fetoprotein, 16,208 ng/mL and des-gamma-carboxy prothrombin, 33,920 mAU/mL. The preoperative diagnosis was malignant tumor of the liver (e.g., HCC or intrahepatic CCA). We performed a left lobectomy of the liver. Histopathologically, the tumor was composed of two components growing in trabecular and irregular tubular patterns accompanied by a transitional area; the tumor was diagnosed as cHCC-CCA. The non-cancerous area showed fibrous change mainly surrounding a central vein and sinusoid, expanding toward the portal area without inflammation. Conclusions: We provide the details of our patient's cHCC-CCA that developed from fibrous congestive liver associated with right-sided heart failure after TOF repair, diagnosed based on histopathological features. We discuss liver fibrosis as a hepatic complication and a careful follow-up maneuver for improving the outcomes of patients with chronic hepatic congestion.. |
| 100. | Narazaki T, Shiratsuchi M, Matsushima T, Tsuda M, Tsukamoto Y, Muta H, Masuda T, Kimura D, Takamatsu A, Yamamoto H, Oda Y, Miyoshi H, Ohshima K, Matsuda Y, Sakamoto R, Nakashima Y, Ogawa Y., Clinico-pathological Characteristics of Primary Adrenal Lymphomas - Potential Efficacy of Autologous Stem Cell Transplantation., Leuk Lymphoma. 1-3, 2020.05. |
| 101. | 井上晃太、立石悠基、本村良知、賀来典之、吉丸耕一朗、山田裕一、孝橋賢一、大賀正一、小田義直 , 病理解剖によって診断し得た川崎病血管炎の一例 , 脈管学. , 2020 May;60(5):71-73, 2020.05. |
| 102. | 堤親範、宮坂義浩、森泰寿、仲田興平、大塚隆生、松田諒太、古賀裕、藤森尚、大野隆真、柿原大輔、小田義直、中村雅史 , １型自己免疫性膵炎を合併しhigh-risk stigmataを呈した膵管内乳頭粘液性腫瘍の1例, 日本消化器外科学会雑誌., 2020 May;53(5):425-434, 2020.05. |
| 103. | Noriko Oyama, Kanako Kojima-Ishii, Naoko Toda, Terumichi Matsuo, Vlad Tocan, Kazuhiro Ohkubo, Utako Oba, Yuhki Koga, Nokitaka Setsu, Yuichi Yamada, Kenichi Kohashi, Yasuharu Nakashima, Yoshinao Oda, Kenji Ihara, Shouichi Ohga, Malignant transformation of phosphaturic mesenchymal tumor:A case report and literature review, Clinical Pediatric Endocrinology, 10.1297/cpe.29.69, 2020.04, [URL], Phosphaturic mesenchymal tumor, mixed connective tissue variant (PMT-MCT) causes tumor-induced osteomalacia (TIO). Most cases follow a benign clinical course, with rare occurrences of malignant transformation. We report a case of malignant PMT-MCT and review previous malignant cases to identify predictive factors for transformation. A 13-yr-old female, who presented with hypophosphatemic rickets, elevated serum intact fibroblast growth factor 23 (FGF23) levels, and a nodule in the back, received a diagnosis of TIO because of the benign PMT histopathology. After resection of the primary tumor, regular imaging analyses did not indicate any relapse. At 17 years of age, a tumor developed in the left leg and increased in size. The resected tumor showed a histopathology of pleomorphic sarcoma positive for the TP53 mutation. Despite amputation of the affected leg, the patient died due to multiple metastases at 18 years of age. A literature review revealed that 14 out of 15 reported malignant PMT-MCT tumors occurred in adults, and found no predictive factors for malignant transformation and treatment outcome. Changes in size or number of the tumors along with intact FGF23 levels have been considered as the only sign of malignant transformation. This pediatric case report and literature review indicate the need for prolonged regular monitoring for PMT-MCT.. |
| 104. | 井上晃太、成富文哉、大城由美、小田義直 , 急性心筋梗塞を発症した超高齢者の血管炎の一剖検例, 脈管学. , 2020 Apr;60(4):57-60, 2020.04. |
| 105. | 成富文哉、山元英崇、小田義直, 免疫組織化学 実践的な診断・治療方針決定のために 免疫組織化学の治療への展開 遺伝子変異特異的抗体, 病理と臨床, 2020 Apr;38(臨時増刊号):384-391, 2020.04. |
| 106. | 山元英崇、石原新、戸田雄、山田裕一、小田義直
, 線維性・線維組織球性骨腫瘍の病理 特集 骨軟部腫瘍の病理Ⅱ, 病理と臨床, 2020 Apr;38(4):320-324, 2020.04. |
| 107. | Kenichi Kohashi, Izumi Kinoshita, Yoshinao Oda, Soft Tissue Special Issue Skeletal Muscle Tumors: A Clinicopathological Review, Head and Neck Pathology, 10.1007/s12105-019-01113-2, 2020.03, [URL], Skeletal muscle tumors are classified into rhabdomyoma and embryonal, alveolar, spindle cell/sclerosing and pleomorphic rhabdomyosarcoma according to WHO classifications of tumors. These tumors arise mostly in the head and neck and, in childhood, represent the largest subset of soft tissue tumors. Although these skeletal muscle tumors show common immunoexpression of two myogenic regulatory factors, MyoD1 and myogenin, their molecular biological backgrounds are quite different. Therefore, treatment regimens vary a great deal depending on the histological subtype. Histopathologically, rhabdomyoma is characterized by well-demarcated lesions with no invasion of the surrounding tissue. Embryonal rhabdomyosarcoma is composed of primitive mesenchymal cells in various stages of myogenesis and shows heterogeneous nuclear staining for myogenin. Alveolar rhabdomyosarcoma, on the other hand, shows a proliferation of uniform primitive round cells arranged in alveolar patterns. The tumor cells at the periphery of alveolar structures adhere in a single layer to the fibrous septa. Diffuse and strong nuclear immunoexpression for myogenin is observed. In genetic backgrounds, almost all alveolar rhabdomyosarcomas contain a characteristic fusion gene such as PAX3/7-FOXO1. Spindle cell/sclerosing rhabdomyosarcoma is characterized by fascicularly arranged spindle-shaped cells or dense hyalinized collagenous matrix. NCOR2- or VGLL2-related gene fusions or MYOD1 (p.L122R) mutation is commonly recognized. Epithelioid rhabdomyosarcoma is a rare variant of rhabdomyosarcoma that shows a proliferation of epithelioid tumor cells having large vesicular nuclei, prominent nucleoli, and amphophilic to eosinophilic cytoplasm arranged in sheets. As these characteristic histological and molecular features are present in each subtype, it is possible to diagnose skeletal muscle tumors accurately.. |
| 108. | Yamamoto H, Ishihara S, Toda Y, Oda Y., Histone H3.3 mutation in giant cell tumor of bone: an update in pathology. , Med Mol Morphol., 53(1):1-6, 2020.03. |
| 109. | 毛利太郎、小田義直, WHO腫瘍組織分類：第5版改訂のポイント 特集 骨軟部腫瘍の病理Ⅰ, 病理と臨床, 38(3):206-210, 2020.03. |
| 110. | 孝橋賢一、小田義直, 特殊な筋原性腫瘍の病理 特集 骨軟部腫瘍の病理I, 病理と臨床, 38(3)226-231, 2020.03. |
| 111. | 小田義直 , 第109回日本病理学会総会のご案内：開催告知, 病理と臨床., 38(3):280-282, 2020.03. |
| 112. | Yamasaki R, Yonekawa T, Inamizu S, Shinoda K, Ochi H, Matsushita T, Isobe N, Tsuji G, Sadashima S, Kuma Y, Oda Y, Iwaki T, Furue M, Kira JI., A case of overlapping adult-onset linear scleroderma and Parry-Romberg syndrome presenting with widespread ipsilateral neurogenic involvement., Neuropathology., 2020.02. |
| 113. | Ueki K, Tsuchimoto A, Matsukuma Y, Torisu K, Fujisaki K, Torisu T, Yamada Y, Oda Y, Masutani K, Nakano T, Tsuruya K, Kitazono T., Hypocomplementemic urticarial vasculitis syndrome with gastrointestinal vasculitis and crescentic membranoproliferative glomerulonephritis without immune complex deposits., CEN Case Rep., 2020.02. |
| 114. | Ono Y, Toyokawa G, Tagawa T, Ijichi K, Oda Y, Mori M., IgG4-Related Lung Disease Exhibiting the Invasion Into the Diaphragm: A Case Report., Ann Thorac Cardiovasc Surg., DOI: 10.5761/atcs.cr.19-00244, PMID: 32101810, 2020.02. |
| 115. | Masakazu Toya, Yuichi Yamada, Ryohei Yokoyama, Kenichi Taguchi, Kazuki Nabeshima, Teruto Isayama, Yoshinao Oda, Dedifferentiated low-grade central osteosarcoma with extensive cystic change initially treated as a simple bone cyst, Pathology Research and Practice, 10.1016/j.prp.2020.152832, 2020.01, [URL], Low-grade central osteosarcoma (LG-COS) is an uncommon variant of osteosarcoma (OS) that sometimes progresses to high-grade OS post-recurrence. We herein present a case of dedifferentiated LG-COS with extensive cystic change arising in the right iliac bone of a 26-year-old man. The LG-COS was initially diagnosed and managed as a simple bone cyst. The lesion recurred thrice, and high-grade OS was diagnosed during the third recurrence. The first lesion appeared as a typical benign cystic mass on radiography. However, a huge malignant osteoblastic mass subsequently developed in the right pelvis at the third recurrence. Extended hemipelvectomy with ipsilateral hemisacral resection was performed. Histologic analysis showed tumor necrosis and irregular neoplastic tumor osteoid, while immunohistochemistry revealed that the tumor was diffusely positive for MDM2 and CDK4. The histologic diagnosis was high-grade OS dedifferentiated from a preceding cystic lesion. Our final diagnosis of the primary lesion was LG-COS with extensive cystic change.. |
| 116. | Yuki Yanagihara, Shintaro Hayashi, Junpei Koge, Hiroyuki Honda, Ryo Yamasaki, Yuichi Yamada, Yoshinao Oda, Toru Iwaki, Jun ichi Kira, Immunotherapy-refractory vacuolar myopathy with mucin deposition in scleromyxedema A possible role of fibroblast growth factor 2, Neuropathology, 10.1111/neup.12659, 2020.01, [URL], Scleromyxedema (SME) is characterized by widespread waxy papules on the skin, with mucin deposits in the upper dermis. Twenty-one SME cases of myopathy have been reported; of the cases, six showed vacuolar formation, and two showed mucin deposition. We report the first case of SME with mucin-containing vacuolated fibers. A 45-year-old woman with SME developed progressive proximal muscle weakness. Muscle biopsy revealed myopathic changes with numerous vacuoles linked to mucin in the affected muscle fibers, which were heavily immunostained for fibroblast growth factor 2 (FGF2). Despite repeated high dose oral prednisolone and intravenous immunoglobulin administrations, muscle weakness recurred continuingly, culminating in death due to congestive heart failure. Immunotherapy was partly effective in our case, although it was refractory. Treatment responsiveness in patients with SME myopathy varied; however, due to its rarity, the mechanism remains to be elucidated. To address this issue, we investigated muscle specimens immunohistochemically and detected marked upregulation of FGF2 in the affected muscle fibers of our patient. FGF2, a strong myogenesis inhibitor, may exert a suppressive effect on muscle fiber regeneration, which may have conferred refractoriness to our patient's SME myopathy.. |
| 117. | Kiyota M, Oya M, Ayano M, Niiro H, Iwasaki T, Fujiwara M, Oda Y, Fujimoto K, Ida H., First Case of Pyrin-Associated Autoinflammation With Neutrophilic Dermatosis Complicated by Amyloidosis., Rheumatology (Oxford)., doi: 10.1093/rheumatology/keaa005., 2020.01. |
| 118. | Tsutsumi C, Moriyama T, Ohuchida K, Shindo K, Nagai S, Yoneda R, Fujiwara M, Oda Y, Nakamura M., Numerous lymph node metastases in early gastric cancer without preoperatively enlarged lymph nodes: a case report., Surg Case Rep., 6(1):30, 2020.01. |
| 119. | 野上美和子、山元英崇、大久保文彦、小田義直, 唾液腺細胞診断におけるミラノシステムの有用性 ―当院における前向き検証―, 日本臨床細胞学会雑誌, 59(1):38-46, 2020.01. |
| 120. | 小田義直 , 希少がんの病理診断体制 骨軟部腫瘍における希少がん病理診断対策とコンサルテーションシステムの試み, 病理と臨床. , 2020 Jan;38(1):53-60, 2020.01. |
| 121. | Yoshino S, Inoue K, Yoshiya K, Kurose S, Nakayama K, Morisaki K, Furuyama T, Matsumoto T, Oda Y, Mori M. 取得済 , Cystic Arterial Disease Located Only in the Media of the Popliteal Artery: A Case Report., Ann Vasc Dis. , 12(4):530-533, 2019.12. |
| 122. | Taisuke Narazaki, Motoaki Shiratsuchi, Mariko Tsuda, Yasuhiro Tsukamoto, Hiroki Muta, Toru Masuda, Daisaku Kimura, Akiko Takamatsu, Ryota Nakanishi, Eiji Oki, Minako Fujiwara, Yoshinao Oda, Yasuhiro Nakashima, Yoshihiro Ogawa, Intestinal Behçet's Disease with Primary Myelofibrosis Involving Trisomy 8, Acta Haematologica, 10.1159/000501019, 2019.11, [URL], Behçet's disease (BD) is a disorder characterized by systemic inflammation of multiple organs, including the intestines. Several studies have reported a relationship between myelodysplastic syndrome and BD, and trisomy 8 was frequently seen, especially in intestinal BD. However, the association of BD with primary myelofibrosis (PMF) has not been well documented. A 58-year-old Japanese female was diagnosed with PMF in 2014. The symptoms of PMF resolved with ruxolitinib. However, she developed fever and intestinal perforation due to multiple ulcers in the terminal ileum in 2017. Intestinal perforation recurred 1 month later, and the dose of ruxolitinib was tapered. After discontinuation of ruxolitinib, she presented with recurrent oral aphthous ulcers and uveitis. Subsequently, intestinal perforation recurred, and she was diagnosed with intestinal BD. Trisomy 8 was identified in her peripheral blood. She underwent steroid therapy, azathioprine, and infliximab. This case suggests relationships between PMF, trisomy 8, and BD.. |
| 123. | Mori T, Yamada Y, Oda Y. , Calcifying Aponeurotic Fibroma. , Encyclopedia of Pathology. , https://doi.org/10.1007/978-3-319-28845-1_5358-1, 2019.11. |
| 124. | Mori T, Yamada Y, Hisaoka M ,Oda Y. , Intranodal Palisaded Myofibroblastoma. , Encyclopedia of Pathology., https://doi.org/10.1007/978-3-319-28845-1_5429-1, 2019.11. |
| 125. | Abe C, Mori T, Yamada Y, Oda Y. , Lymphangioma, Soft Tissue. , Encyclopedia of Pathology. , https://doi.org/10.1007/978-3-319-28845-1_5487-1, 2019.11. |
| 126. | 清澤大裕、山田裕一、小田義直 , 胸膜の中皮腫以外の腫瘍性疾患, 病理と臨床, 37(11):1089-1096, 2019.11. |
| 127. | 佐伯潔、大石善丈、崎濱久紀子、山本猛雄、松田諒太、宮坂義浩、中村雅史、小田義直, 唾液腺型粘表皮癌様の形態学的特徴を有する膵腺扁平上皮癌の１症例, 診断病理, 2019.10. |
| 128. | Masuda Y, Tsukamoto Y, Zenitani M, Oda Y, Kinoshita I, Kohashi K, Takemoto J, Hirota S, Shibata A, Koda T, Takeshima Y. , A newborn case of jejunal ALK-negative inflammatory myofibroblastic tumor with ETV6-NTRK3 fusion., Pediatr Blood Cancer. , 66(10):e27902, 2019.10. |
| 129. | Yamamoto M, Yoshida Y, Tuneyoshi M, Gion T, Tominaga Y, Koga Y, Oda Y, Gastric Perivascular Epithelioid Cell Tumor: A Case Report", Ann Case Report, 2019.09. |
| 130. | Wang H, Yoshizumi T, Itoh S, Ikegami T, Harada N, Oda Y, Mori M. , Retroperitoneal schwannoma preoperatively diagnosed as liver metastasis from colon cancer: A case report., Int J Surg Case Rep., 2019.09. |
| 131. | 小田義直 , 良性および中間悪性骨腫瘍の病理診断における分子医学的アプローチ, 病理と臨床, 37(9):902-904, 2019.09. |
| 132. | Yorita K, Togashi Y, Nakagawa H, Miyazaki K, Sakata S, Baba S, Takeuchi K, Hayashi Y, Murakami I, Kuroda N, Oda Y, Kohashi K, Yamada Y, Kiyozawa D, Michal M, Michal M. , Vocal cord inflammatory myofibroblastic tumor with mucoid deposits harboring TIMP3-ALK fusion: A potential diagnostic pitfall. , Pathol Int. , 69(6):366-371, 2019.06. |
| 133. | Aya Izuwa, Gouji Toyokawa, Fumihiro Shoji, Koji Yamazaki, Seiya Momosaki, Kiyomi Furuya, Yuichi Yamada, Yoshinao Oda, Sadanori Takeo, First Case of a Primary Lung Granulosa Cell Tumor With a Mutation in the Forkhead Box L2 Gene, Journal of Thoracic Oncology, 10.1016/j.jtho.2018.12.029, 2019.05, [URL]. |
| 134. | Kenji Miki, Koji Yoshimoto, Yuichi Yamada, Akira Kabashima, Daisuke Kuga, Yoshinao Oda, Koji Iihara, Rapid growth of metastatic brain tumor from gastric undifferentiated pleomorphic sarcoma A case report, Surgical Neurology International, 10.25259/SNI-84-2019, 2019.04, [URL], Background: Brain metastasis from undifferentiated pleomorphic sarcoma (UPS) is a rare occurrence, and its clinical course is little known. In this report, we investigate a case of a rapidly growing brain metastasis from gastric UPS. Case Description: An 82-year-old man with a known gastric tumor, pathologically compatible with UPS, underwent partial gastrectomy at an outside facility. 3 months later, a 4-cm brain tumor was detected, which was completely resected. The patient was diagnosed with metastatic tumor from previously treated gastric UPS. Within 2 months of the initial resection, a large recurrent mass was detected in the same location, which was again removed. Although the patient underwent radiotherapy and chemotherapy for other metastatic tumors, he died 5 months after the second craniotomy. Conclusions: Brain metastasis from gastric UPS is rare and difficult to treat. Although aggressive treatment, such as surgical intervention, may improve patient survival in some cases, the timing of treatment is challenging because cerebral metastasis rapidly grows and and patients frequently suffer from synchronous systematic metastasis. Therefore, early detection and close follow-up of rapidly progressing brain metastasis are important to improve treatment outcomes.. |
| 135. | Yugawa K, Yoshizumi T, Mano Y, Kurihara T, Yoshiya S, Takeishi K, Itoh S, Harada N, Ikegami T, Soejima Y, Kohashi K, Oda Y, Mori M. , Solitary fibrous tumor in the liver: case report and literature review., Surg Case Rep., 2019.04. |
| 136. | 戸田雄、小田義直
, 類軟骨骨化を来す腫瘍と軟骨肉腫の亜型の鑑別 【画像診断】骨・軟部腫瘍の鑑別診断のポイント, 画像診断増刊号, 2019.03. |
| 137. | Takeshi Iwasaki, Hidetaka Yamamoto, Yoshinao Oda, Current Update on the Molecular Biology of Cutaneous Sarcoma Dermatofibrosarcoma Protuberans, Current Treatment Options in Oncology, 10.1007/s11864-019-0628-3, 2019.03, [URL], Cutaneous sarcoma is a group of malignant mesenchymal tumors primarily involving the dermis, and it is characterized by extreme clinicopathological heterogeneity. Although its occurrence rate is rare, dermatofibrosarcoma protuberans (DFSP) is one of the most common types of dermal sarcoma. DFSP grows slowly and tends to relapse locally after inadequate resection. There are various histological variants of DFSP tumors and it often mimics benign lesions such as dermatofibroma and scar, which make accurate diagnosis difficult and delayed, and some cases progress to the stage where the tumor is unresectable. Recent advancements in cancer genetics and molecular biology methods have elucidated the COL1A1-PDGFB fusion gene, some novel fusion gene variants and pathways related to DFSP pathogenesis that have resulted in the evolution of cutaneous sarcoma diagnosis and treatment. For example, some clinical studies have confirmed the efficacy of imatinib methylate, an αPDGFR-targeted therapy for unresectable or metastatic DFSP. The present review summarizes recent updates in DFSP research, diagnostics, and treatment.. |
| 138. | Takashi Okumura, Kenoki Ohuchida, Shin Kibe, Chika Iwamoto, Yohei Ando, Shin Takesue, Hiromichi Nakayama, Toshiya Abe, Sho Endo, Kazuhiro Koikawa, Masafumi Sada, Kohei Horioka, Naoki Mochidome, Makoto Arita, Taiki Moriyama, Kohei Nakata, Yoshihiro Miyasaka, Takao Ohtsuka, Kazuhiro Mizumoto, Yoshinao Oda, Makoto Hashizume, Masafumi Nakamura, Adipose tissue-derived stromal cells are sources of cancer-associated fibroblasts and enhance tumor progression by dense collagen matrix, International Journal of Cancer, 10.1002/ijc.31775, 2019.03, [URL], Although recent studies revealed that adipose tissue accelerates pancreatic tumor progression with excessive extracellular matrix, key players for desmoplasia in the adipose microenvironment remains unknown. Here, we investigated the roles of adipose tissue-derived stromal cells (ASCs) in desmoplastic lesions and tumor progression by in vitro and in vivo experiments. In a three-dimensional (3-D) organotypic fat invasion model using visceral fat from CAG-EGFP mice, GFP-positive fibroblastic cells infiltrated toward cancer cells. When tumor cells were inoculated into transplanted visceral fat pads in vivo, tumor weights and stromal components were enhanced compared to subcutaneous and orthotopic tumor cells inoculated without fat pads. Expression of αSMA in established human ASCs was lower compared to cancer associated fibroblasts, and the 3-D collagen matrices produced by ASCs cultured in cancer cell-conditioned medium changed from loose to dense structures that affected the motility of cancer cells. Microarray analyses revealed upregulation of S100A4 in ASCs, while S100A4-positive stromal cells were observed at extrapancreatic invasion sites of human pancreatic cancer. The present findings indicate that ASCs are recruited to extrapancreatic invasion sites and produce dense collagen matrices that lead to enhanced tumor progression. Both inhibition of ASCs recruitment and activation could lead to a novel antistromal therapy.. |
| 139. | Shin Kibe, Kenoki Ohuchida, Yohei Ando, Shin Takesue, Hiromichi Nakayama, Toshiya Abe, Sho Endo, Kazuhiro Koikawa, Takashi Okumura, Chika Iwamoto, Koji Shindo, Taiki Moriyama, Kohei Nakata, Yoshihiro Miyasaka, Masaya Shimamoto, Takao Ohtsuka, Kazuhiro Mizumoto, Yoshinao Oda, Masafumi Nakamura, Cancer-associated acinar-to-ductal metaplasia within the invasive front of pancreatic cancer contributes to local invasion, Cancer Letters, 10.1016/j.canlet.2018.12.005, 2019.03, [URL], The pancreas is an organ prone to inflammation, fibrosis, and atrophy because of an abundance of acinar cells that produce digestive enzymes. A characteristic of pancreatic cancer is the presence of desmoplasia, inflammatory cell infiltration, and cancer-associated acinar atrophy (CAA) within the invasive front. CAA is characterized by a high frequency of small ducts and resembles acinar-to-ductal metaplasia (ADM). However, the clinical significance of changes in acinar morphology, such as ADM with acinar atrophy, within the tumor microenvironment remains unclear. Here, we find that ADM within the invasive front of tumors is associated with cell invasion and desmoplasia in an orthotopic mouse model of pancreatic cancer. An analysis of resected human tumors revealed that regions of cancer-associated ADM were positive for TGFα and that this TGFα expression was associated with primary tumor size and shorter survival times. Gene expression analysis identified distinct phenotypic profiles for cancer-associated ADM, sporadic ADM and chronic pancreatitis ADM. These findings suggest that the mechanisms driving ADM differ according to the specific tissue microenvironment and that cancer-associated ADM and acinar atrophy contribute to tumor cell invasion of the local pancreatic parenchyma.. |
| 140. | Yuichi Shibui, Kina Miyoshi, Kenichi Kohashi, Yoshiaki Kinoshita, Masaaki Kuda, Hidetaka Yamamoto, Tomoaki Taguchi, Yoshinao Oda, Glypican-3 expression in malignant small round cell tumors, Oncology Letters, 10.3892/ol.2019.9976, 2019.03, [URL], Malignant small round cell tumors usually progress rapidly and show resistance to chemotherapy, and it is often difficult to make a definitive diagnosis based on their histological morphology. Glypican-3 (GPC3) is a highly tumor-specific antigen, and the overexpression of GPC3 was reported in many pediatric and adult malignancies. In the present study, we investigated the GPC3 expression in pediatric malignant small round cell tumors to assess its role in the differential diagnosis of the tumors. Immunohistochemistry was performed to assess the expression of GPC3 in samples from 84 rhabdomyosarcomas (RMSs; 44 alveolar and 40 embryonal RMSs), 62 Ewing sarcomas (EWSs), 35 neuroblastomas (NBs) and two desmoplastic small round cell tumors (DSRCTs). We performed a reverse transcription-quantitative polymerase chain reaction for GPC3 to determine the GPC3 mRNA expression in samples from 66 frozen tumors (23 RMSs, 28 EWSs and 15 NBs). The serum expression levels of GPC3 were analyzed in pre-operative blood samples from two RMS and eight NB patients. In total, 25% (21/84) of the RMSs and 3% (1/35) of the NBs exhibited a focal expression of GPC3, whereas, the other specimens showed no GPC3 expression. The GPC3 mRNA expression level of the RMSs with positive GPC3 expression (n=6) was significantly higher compared with the RMSs without such expression (n=17). A total of two cases of NB showed high serum levels of GPC3, but neither tumor showed immunoreactivity for GPC3. The immunohistochemical overexpression of GPC3 may be a candidate ancillary parameter in the differential diagnosis of RMS from EWS and DSRCT.. |
| 141. | Junkichi Takemoto, Masaaki Kuda, Kenichi Kohashi, Yuichi Yamada, Yutaka Koga, Izumi Kinoshita, Ryota Souzaki, Tomoaki Taguchi, Yoshinao Oda, HuC/D expression in small round cell tumors and neuroendocrine tumors a useful tool for distinguishing neuroblastoma from childhood small round cell tumors, Human Pathology, 10.1016/j.humpath.2018.11.004, 2019.03, [URL], The RNA-binding protein HuC/D displays a neuron-specific expression and is involved in neuronal differentiation and the maintenance of the nervous system. Here we investigated the diagnostic value of HuC/D in neuroblastomas. We evaluated 85 neuroblastic tumors: 81 neuroblastomas; 3 ganglioneuroblastomas, intermixed; 1 ganglioneuroma, maturing; and 101 other tumors consisting of 34 Ewing sarcomas, 14 nephroblastomas, 11 rhabdomyosarcomas, 15 pulmonary small cell carcinomas, 18 pancreatic neuroendocrine tumors, and 9 pheochromocytomas. Immunohistochemistry for HuC/D, PHOX2B, and tyrosine hydroxylase was performed. The immunoreactivity for HuC/D was semiquantified using the total score (TS; range, 0-8). HuC/D positivity was defined as a TS ≥6. The TS of the neuroblastic tumors (mean TS, 7.94) was significantly higher than those of the other small round cell tumors and neuroendocrine tumors (P |
| 142. | Yuichi Shibui, Kenichi Kohashi, Ichiro Sakamoto, Kenichiro Yamamura, Yoshinao Oda, Intrahepatic cholangiocarcinoma after the Fontan procedure, Human Pathology: Case Reports, 10.1016/j.ehpc.2018.10.008, 2019.03, [URL], A long duration of Fontan circulation can cause fibrosis, cirrhosis of the liver and liver cancer. There have been some reports of hepatocellular carcinoma occurring after the Fontan procedure (FP), and we encountered a case of intrahepatic cholangiocarcinoma (ICC) after the FP. We herein report the case of 33-year-old man who developed ICC after receiving the FP. At five years of age, the patient underwent the original FP. At 16 years of age, he received total cavopulmonary connection conversion. Sixteen years later, he suffered right heart failure. Thereafter his symptoms showed repeated exacerbation and remission. One year later, he was admitted to the hospital due to the aggravation of congestive heart failure symptoms. He developed contrast nephropathy, and his renal function rapidly weakened. Computed tomography revealed multiple mass lesions in the liver. He ultimately died four months after his admission. An autopsy revealed the hepatic tumor to be ICC. Patients who have undergone the FP need to undergo a checkup with ultrasound on a regular basis.. |
| 143. | Yoshihiro Komohara, Hiroto Takeya, Nanako Wakigami, Natsuki Kusada, Hirofumi Bekki, Shin Ishihara, Motohiro Takeya, Yasuharu Nakashima, Yoshinao Oda, Positive correlation between the density of macrophages and T-cells in undifferentiated sarcoma, Medical Molecular Morphology, 10.1007/s00795-018-0201-3, 2019.03, [URL], Undifferentiated sarcoma (US) is a frequent soft tissue sarcoma. Although the 10-year survival rate is around 60%, advanced US is highly resistant to chemo/radiotherapy. The tumor microenvironment (TME) is closely associated with tumor progression. However, few studies of infiltrated immune cells in US have been published. In this study, we evaluated tumor-associated macrophages (TAMs) and CD8-positive cytotoxic T lymphocytes (CTLs) in 28 cases of US. Iba1, CD163, and CD204 were used as markers for TAMs. The density of CTLs was positively correlated with the density of TAMs. However, a negative correlation was seen between the density of CTLs and the percentage of CD204-positive TAMs. We found no significant association between the density of Iba1-/CD204-/CD8-positive cells and clinicopathological factors. No significant correlation between immune cell infiltration and clinical outcome was observed. Although we found no significant association between immune cells and clinicopathological factors, these findings may provide new insight into the characterization of immune cells in the TME of US.. |
| 144. | Yasuaki Hagio, Akira Shiraishi, Masataka Ishimura, Motoshi Sonoda, Katsuhide Eguchi, Hidetaka Yamamoto, Yoshinao Oda, Shouichi Ohga, Posttransplant recipient-derived CD4 + T-cell lymphoproliferative disease in X-linked hyper-IgM syndrome, Pediatric Blood and Cancer, 10.1002/pbc.27529, 2019.03, [URL]. |
| 145. | Yu Nakaji, Hiroshi Saeki, Kensuke Kudou, Ryota Nakanishi, Masahiko Sugiyama, Yuichiro Nakashima, Koji Ando, Yoshinao Oda, Eiji Oki, Yoshihiko Maehara, Short- and long-term outcomes of surgical treatment for remnant gastric cancer after distal gastrectomy, Anticancer research, 10.21873/anticanres.13256, 2019.03, [URL], Background/Aim: Remnant gastric cancer (RGC) after distal gastrectomy occurs in 1-2% of patients, while the biological features of RGC are unknown. Patients and Methods: A total of 22 consecutive patients with RGC who underwent total gastrectomy were analyzed. Their disease history included either gastric cancer (n=16) or peptic ulcer (n=6). Overall, 18 underwent open total gastrectomy (OTG) and 4 underwent laparoscopic total gastrectomy (LTG). Results: The mean number of lymph nodes dissected and metastatic lymph nodes was larger in the Ulcer group than in the Carcinoma group (p |
| 146. | Hirose K, Saeki H, Nakashima Y, Kamori T, Fujimoto Y, Kawazoe T, Matsuoka H, Haruta Y, Sasaki S, Jogo T, Hu Q, Tsuda Y, Ando K, Oki E, Hiratsuka R, Oda Y, Mori M. , Successful multidisciplinary treatment including repeated metastasectomy for recurrent squamous cell esophageal carcinoma: a case report., Surg Case Rep., 2019.03. |
| 147. | 藤原美奈子、保利喜史、古賀裕、小田義直, 腸管感染症の診断における生検組織の役割, INTESTINE 日本メディカルセンター, 2019.03. |
| 148. | Gouji Toyokawa, Kazuki Takada, Tetsuzo Tagawa, Ryuji Hamamoto, Yuichi Yamada, Mototsugu Shimokawa, Yoshinao Oda, Yoshihiko Maehara, A Positive Correlation Between the EZH2 and PD-L1 Expression in Resected Lung Adenocarcinomas, Annals of Thoracic Surgery, 10.1016/j.athoracsur.2018.08.056, 2019.02, [URL], Background: Enhancer of zeste homolog 2 (EZH2) is reported to be involved in lung cancer pathogenesis via the epigenetic regulation of various genes. Recently, EZH2 was shown to control mechanisms of adaptive resistance to immunotherapy in melanoma; however, the association between EZH2 and programmed death-ligand 1 (PD-L1), which reflects the tumor microenvironment, remains poorly understood. Methods: A total of 428 patients with resected lung adenocarcinoma were analyzed for their EZH2 and PD-L1 expression by immunohistochemistry and evaluated to determine the association between the EZH2 and PD-L1 expression. Results: Among 428 patients, the EZH2 expression was identified in 219 (51.2%) patients, while the PD-L1 expression was observed in 88 (20.6%) patients. The recurrence-free and overall survival were significantly shorter in patients with the EZH2 expression than in those without it. A multivariate analysis showed that EZH2 remained an independent prognosticator for recurrence-free and overall survival. Patients with the EZH2-positive lung adenocarcinoma exhibited a significantly higher expression of PD-L1 than did those without it. A logistic regression analysis with backward elimination revealed that the presence of lymphatic and vessel invasion and PD-L1 positivity were independently associated with the EZH2 expression, while age over 70 years, the presence of vessel invasion, wild-type epidermal growth factor receptor, and EZH2 positivity were significantly associated with the PD-L1 expression. Conclusions: EZH2-expressing lung adenocarcinomas were shown to express the PD-L1 protein more frequently than were nonexpressing lesions. This study provides the first evidence of a possible association between the EZH2 and PD-L1 expression in patients with resected lung adenocarcinoma.. |
| 149. | Satoshi Obata, Koichiro Yoshimaru, Kosuke Kirino, Tomoko Izaki, Satoshi Ieiri, Atsuyuki Yamataka, Tsugumichi Koshinaga, Jun Iwai, Hitoshi Ikeda, Hiroshi Matsufuji, Yoshinao Oda, Tomoaki Taguchi, Acquired isolated hypoganglionosis as a distinct entity results from a nationwide survey, Pediatric surgery international, 10.1007/s00383-018-4398-y, 2019.02, [URL], Purpose: Acquired isolated hypoganglionosis (A-IH) is a late-onset intestinal pseudo-obstruction disorder and shows different pathophysiological findings from congenital isolated hypoganglionosis (C-IH). In this study, we retrospectively examined five cases of A-IH and investigated the features of A-IH. Methods: Five cases of A-IH were extracted from a nationwide retrospective cohort study in 10 years, from which totally 355 cases of Allied Disorders of Hirschsprung’s Disease (ADHD) were collected. Results: Ages of onset were between 13 and 17 years in three cases, and 4 years and 4 months in ones. Initial symptoms were abdominal distension and/or chronic constipation in 4 cases, whereas one exhibited intestinal perforation. Affected lesions varied from case to case, extending various length of intestinal tracts. All cases underwent multiple operations (average: 4.6 times), such as enterostomy, resection of dilated intestines, and/or pull-through. Pathological findings showed the decreased numbers of ganglion cells and degeneration of ganglion cells, whereas the size of the plexus was normal. Currently, all cases were alive and almost all eat regular food without requiring parenteral feeding. Conclusion: A-IH is rare, but distinct entity characterized by different clinical courses and pathological findings from those of C-IH. The outcome is considered to be favorable after a resection of affected intestine.. |
| 150. | Kazuki Takada, Kenichi Kohashi, Mototsugu Shimokawa, Akira Haro, Atsushi Osoegawa, Tetsuzo Tagawa, Takashi Seto, Yoshinao Oda, Yoshihiko Maehara, Co-expression of IDO1 and PD-L1 in lung squamous cell carcinoma Potential targets of novel combination therapy, Lung Cancer, 10.1016/j.lungcan.2018.12.008, 2019.02, [URL], Objectives: Combination therapy with an inhibitor of indoleamine 2, 3-dioxygenase 1 (IDO1) and an agent targeting programmed cell death-1 (PD-1)/programmed cell death-ligand 1 (PD-L1) is expected to be a novel and effective treatment option for various solid tumors including non-small cell lung cancer (NSCLC). Therefore, it is important to elucidate the clinical and pathological features of tumors with IDO1/PD-L1 co-expression and the association between IDO1/PD-L1 co-expression and efficacy of combination therapy in NSCLC patients. In this study, we examined the prognostic impact of IDO1/PD-L1 co-expression and its relationship with tumor-infiltrating lymphocytes (TILs) in primary lung squamous cell carcinoma (SCC). Materials and methods: The expression levels of IDO1, PD-L1, Ki-67, cluster of differentiation 3 (CD3), CD4, and CD8 in 202 patients with surgically resected primary lung SCC were evaluated by immunohistochemistry. Results: Among 202 patients, 176 (87.1%) were positive for IDO1 expression, 106 (52.5%) were positive for PD-L1 expression, and 99 (49.0%) showed co-expression of IDO1/PD-L1 proteins. Fisher's exact test showed a significant association between IDO1 and PD-L1 tumor proportion scores (P = 0.0011). Kaplan–Meier curve showed that PD-L1 alone and co-expression of IDO1 and PD-L1 were significantly associated with shorter overall survival, but IDO1 alone was not (log rank test: P = 0.0122, P = 0.0303 and P = 0.5168, respectively). The Ki-67 labeling index was significantly higher in patients with co-expression of IDO1 and PD-L1 than in patients without co-expression (Student's t-test: P = 0.0005). Moreover, IDO1/PD-L1 co-expression was significantly associated with high CD3, CD4, and CD8 expression (Fisher's exact test: P = 0.0033, P = 0.0003, and P |
| 151. | Yoshikawa N, Tazaki T, Hatanaka M, Oda Y, Matsumoto N, Sonoda J, Ikeda R. , Drug-drug interactions among drugs prescribed for nontuberculous mycobacterial infection and epilepsy: A case report., J Clin Pharm Ther., 2019.02. |
| 152. | Yasuyuki Masuda, Yoshitane Tsukamoto, Masahiro Zenitani, Yoshinao Oda, Izumi Kinoshita, Kenichi Kohashi, Junkichi Takemoto, Seiichi Hirota, Akio Shibata, Tsubasa Koda, Yasuhiro Takeshima, A newborn case of jejunal ALK-negative inflammatory myofibroblastic tumor with ETV6-NTRK3 fusion, Pediatric Blood and Cancer, 10.1002/pbc.27902, 2019.01, [URL]. |
| 153. | Shinkichi Takamori, Gouji Toyokawa, Mototsugu Shimokawa, Fumihiko Kinoshita, Yuka Kozuma, Taichi Matsubara, Naoki Haratake, Takaki Akamine, Fumihiko Hirai, Tetsuzo Tagawa, Yoshinao Oda, Yoshihiko Maehara, A novel prognostic marker in patients with non-small cell lung cancer Musculo-immuno-nutritional score calculated by controlling nutritional status and creatine kinase, Journal of Thoracic Disease, 10.21037/jtd.2019.01.76, 2019.01, [URL], Background: Controlling nutritional status (CONUT) and skeletal muscle area (SMA) are both useful prognostic factors in patients with non-small cell lung cancer (NSCLC). We hypothesized that low serum creatine kinase (CK) would be a surrogate of decreased SMA, and defined a novel prognostic factor, CONUT/CK score (CNKS). The aim of this study was to elucidate the clinical significance of CNKS in NSCLC patients. Methods: One hundred and eighty-nine patients who underwent surgical resection of NSCLC and whose preoperative computed tomography images were available were enrolled. The CNKS was calculated by summing CONUT score and CK score, which was defined as 0 if the CK concentration is within normal range, and 2 if it is under lower limit. The optimal cut-off values of CNKS and CONUT score were 4 and 2, respectively. Results: Low CK was significantly associated with decreased SMA (P=0.012). The high CNKS group was significantly associated with men and smoking history (P=0.006 and P=0.015, respectively). The high CNKS group had significantly shorter overall survival (OS) and disease-free survival (DFS) (P |
| 154. | Yutaka Koga, Minako Hirahashi, Yoshihiro Ohishi, Yoshinao Oda, Clinicopathological features and phenotypic classification of de novo-type colorectal carcinomas differ from those of colorectal carcinomas derived from flat adenomas, Pathology International, 10.1111/pin.12803, 2019.01, [URL], Since adenoma components disappear with tumor progression, it is not known whether colorectal carcinomas (CRCs) are derived from an adenoma–carcinoma sequence or are de novo. We compared 38 cases of ≤10-mm flat CRCs without an adenoma component (de novo type) with 39 cases of ≤10-mm flat CRCs with an adenoma component (carcinoma in adenoma (CIA) type). Compared to the CIA type, the de novo-type CRCs were more frequently located in the proximal colon; more frequently invaded submucosa, and more frequently had venous permeation. Regarding the phenotypic classification based on the immunohistochemical expressions of CD10, MUC2 and MUC5AC, the incidence of unclassified type (CD10−, MUC2− and MUC5AC−) was significantly more frequent in the de novo (32%) than CIA (5%) type. In one de novo-type case, mismatch repair (MMR) protein loss was judged, because MLH1 and PMS2 protein expressions were immunohistochemically negative. BRAF mutation (V600E) was seen in one de novo-type case and two CIA-type cases, but none of these cases had MMR protein loss. In conclusion, small-intestinal type (CD10+ and MUC5AC−) is the most common in flat CRC and unclassified type is mainly characteristic of de novo type. In this study, small flat CRCs with BRAF mutation do not have MMR protein loss.. |
| 155. | Masato Yoshimoto, Yuichi Yamada, Shin Ishihara, Kenichi Kohashi, Yu Toda, Yoshihiro Ito, Hidetaka Yamamoto, Masutaka Furue, Yasuharu Nakashima, Yoshinao Oda, Comparative study of myxofibrosarcoma with undifferentiated pleomorphic sarcoma Histopathologic and clinicopathologic review, American Journal of Surgical Pathology, 10.1097/PAS.0000000000001389, 2019.01, [URL], Myxofibrosarcoma (MFS) is a malignant fibroblastic/ myofibroblastic neoplasm with the prominent myxoid area. It has the clinical features of frequent local recurrence and occasional distant metastasis. Morphologically, MFS is occasionally difficult to distinguish from undifferentiated pleomorphic sarcoma (UPS), especially in the case of high-grade MFS. Here, we reviewed clinical and histologic data of 162 MFS cases and 43 UPS cases. MFS was distinguished from UPS with the criterion of 10% myxoid area as a cutoff value. Overall, 52MFS (34.4%) and 9 UPS (20.9%) cases showed local recurrence, 18 MFS (12.2%) and 19 UPS (44.2%) cases developed distant metastasis, and 13 MFS (9.5%) and 14 UPS (32.6%) cases resulted in tumor-related death. Statistically, MFS had a better prognosis than UPS. Moreover, MFS with less myxoid area had a tendency to present a poorer prognosis. FNCLCC grade was a statistically significant prognostic factor (distant metastasis: P=0.0021, tumor-related death: P=0.0021). Cellularity and nuclear atypia had only a statistical tendency for associations with a poorer prognosis. The overall survival rate of MFS after transformation into a UPS-like condition ( |
| 156. | Rina Jiromaru, Hidetaka Yamamoto, Ryuji Yasumatsu, Takahiro Hongo, Yui Nozaki, Kazuki Hashimoto, Kenichi Taguchi, Muneyuki Masuda, Takashi Nakagawa, Yoshinao Oda, HPV-related Sinonasal Carcinoma Clinicopathologic Features, Diagnostic Utility of p16 and Rb Immunohistochemistry, and EGFR Copy Number Alteration, American Journal of Surgical Pathology, 10.1097/PAS.0000000000001410, 2019.01, [URL], The prevalence and prognostic value of human papillomavirus (HPV) infection and epidermal growth factor receptor (EGFR) alteration in sinonasal squamous cell carcinoma (SNSCC) are not known. The reliability of p16 overexpression as a surrogate for HPV infection in SNSCC is also unclear. We investigated the prognostic and diagnostic significances of HPV infection, EGFR alteration, and p16 expression in SNSCC. We analyzed high-risk HPV infection by HPV-RNA in situ hybridization and EGFR gene copy number gain (CNG) by chromogenic in situ hybridization and by determining the protein expressions of p16, Rb, and EGFR by immunohistochemistry in 101 SNSCC cases. HPV infection (n=9, 8.9%) and p16 overexpression (n=15, 14.9%) were associated with better overall survival (P=0.0042 and 0.005, respectively). The HPV+ cases were located predominantly at the nasal cavity with nonkeratinizing histology and partial loss of Rb. Notably, 40% (6/15) of p16+ SNSCCs were HPV-. Two of these cases showed complete loss of Rb expression by immunohistochemistry, suggesting a reason for the above discrepancy. EGFR CNG, detected in 30.5% of the SNSCCs, was correlated with EGFR protein overexpression (P=0.0001). HPV infection and EGFR CNG were mutually exclusive. The HPV+/EGFR CNG- group had significantly better overall survival than the HPV-/EGFR CNG- and HPV-/EGFR CNG+ groups (P=0.0471 and 0.0343, respectively). Our results suggest that HPV infection is a favorable prognostic marker in SNSCC, but p16 is not a perfect surrogate marker; the Rb expression pattern may improve the diagnostic accuracy. The molecular subclassification of SNSCCs based on HPV infection and EGFR copy number status might provide important information for therapeutic strategies.. |
| 157. | Hidetaka Yamamoto, Shin Ishihara, Yu Toda, Yoshinao Oda, Histone H3.3 mutation in giant cell tumor of bone an update in pathology, Medical Molecular Morphology, 10.1007/s00795-019-00238-1, 2019.01, [URL], Giant cell tumor of bone (GCTB) is a locally aggressive bone tumor that frequently shows local recurrence and occasionally shows malignant transformation to high-grade sarcoma. Histologically, conventional GCTB is composed mainly of three types of cells: mononuclear neoplastic cells with an osteoblastic precursor phenotype, mononuclear histiocytic cells, and osteoclast-like multinucleated giant cells. These cells interact with each other via the RANKL-RANK axis and other mechanisms for tumor formation. The vast majority of GCTBs were recently revealed to harbor H3F3A p.G34W mutation, and a minor subset have H3F3A p.G34L, p.G34M, p.G34R, or p.G34V mutation. H3.3 G34W mutant-specific immunohistochemistry is a highly sensitive and specific surrogate marker for H3F3A p.G34W mutation in GCTB and thus useful for differential diagnoses of histological mimics. H3.3 mutant-specific immunohistochemistry has also contributed to the understanding of the bone-forming ability of neoplastic cells of GCTB and the remarkable new bone formation after treatment with denosumab, an inhibitor of RANKL. In primary and secondary malignant GCTBs, the H3F3A gene allele can be preserved or lost with malignant transformation.. |
| 158. | Yuka Kozuma, Gouji Toyokawa, Yuichi Yamada, Fumihiro Shoji, Koji Yamazaki, Yoshinao Oda, Sadanori Takeo, Spread through air spaces in non-small cell lung cancer, Journal of Thoracic Disease, 10.21037/jtd.2019.08.97, 2019.01, [URL]. |
| 159. | Kenji Yorita, Yuki Togashi, Hideyuki Nakagawa, Katsushi Miyazaki, Seiji Sakata, Satoko Baba, Kengo Takeuchi, Yoshihiro Hayashi, Ichiro Murakami, Naoto Kuroda, Yoshinao Oda, Kenichi Kohashi, Yuichi Yamada, Daisuke Kiyozawa, Michael Michal, Michal Michal, Vocal cord inflammatory myofibroblastic tumor with mucoid deposits harboring TIMP3–ALK fusion A potential diagnostic pitfall, Pathology International, 10.1111/pin.12796, 2019.01, [URL], A 35-year-old Japanese man who had experienced hoarseness for 10 years presented with a vocal cord lesion. A gross examination revealed a left vocal cord polyp occupying two-thirds of the vocal space. The endoscopically resected lesion contained scattered atypical fibroblastic, stellate, or ganglion-like cells with mucoid stroma. Vacuolated cells were also seen. Lymphoplasmacytic infiltrate was largely undetectable. A vocal cord polyp was first suspected, but well-differentiated liposarcoma and inflammatory myofibroblastic tumor (IMT) were included in the differential diagnoses. The tumor cells were positive for anaplastic lymphoma kinase (ALK), calponin, and vimentin, and negative for other smooth muscle markers by immunohistochemistry. Structures resembling myofibroblasts were not observed by electron microscopy, which confirmed abundant rough endoplasmic reticulum in the tumor cells and accumulated lipid droplets in some tumor cells. ALK gene rearrangement was detected by fluorescence in situ hybridization, and TIMP3–ALK fusion was confirmed by 5′ rapid amplification of cDNA ends. We diagnosed the lesion as an IMT, and an ALK-rearranged stellate cell tumor may be postulated. This is the first report of a fusion partner gene of ALK in a case of laryngeal IMT.. |
| 160. | Chihiro Sakaguchi, Kenji Ashida, Kenichi Kohashi, Kenji Ohe, Yoichi Fujii, Seiichi Yano, Yayoi Matsuda, Shohei Sakamoto, Ryuichi Sakamoto, Yoshinao Oda, Masatoshi Nomura, Yoshihiro Ogawa, A case of autonomous cortisol secretion in a patient with subclinical Cushing's syndrome, GNAS mutation, and paradoxical cortisol response to dexamethasone, BMC Endocrine Disorders, 10.1186/s12902-019-0345-8, 2019.01, [URL], Background: Increased urinary free cortisol in response to the oral administration of dexamethasone is a paradoxical reaction mainly reported in patients with primary pigmented nodular adrenocortical disease. Here, we describe the first case of subclinical Cushing's syndrome represented by autonomous cortisol secretion and paradoxical response to oral dexamethasone administration, harboring an activating mutation in the α subunit of the stimulatory G protein (GNAS). Case presentation: A 65-year-old woman was diagnosed with subclinical Cushing's syndrome during an evaluation for bilateral adrenal masses. Tumors of unknown origin were found in the heart, brain, thyroid gland, colon, pancreas, and both adrenal glands. Adenocarcinoma of the sigmoid colon and systemic brown-patchy skin pigmentation were also present. Her urinary cortisol levels increased in response to oral dexamethasone, while serum dehydroepiandrosterone-sulfate was not suppressed. After right adrenalectomy, genetic analysis of the resected tumor revealed the somatic GNAS activating mutation, p.R201H. Paradoxical urinary cortisol response persisted even after unilateral adrenal resection, although serum and urinary cortisol levels were attenuated. Conclusions: This patient harbored a GNAS activating mutation, and presented with a mild cortisol- and androgen-producing adrenal adenoma. Administration of oral dexamethasone paradoxically increased cortisol levels, possibly via the stimulation of the cyclic adenosine monophosphate-dependent protein kinase A signaling pathway, which is seen in patients with pigmented nodular adrenocortical disease or Carney complex. GNAS mutations may provide clues to the mechanisms of hyper-function and tumorigenesis in the adrenal cortex, especially in bilateral adrenal masses accompanied by multiple systemic tumors. Examining GNAS mutations could help physicians detect extra-adrenal malignancies, which may contribute to an improved prognosis for patients with this type of Cushing's syndrome.. |
| 161. | Yasuyuki Masuda, Yoshitane Tsukamoto, Masahiro Zenitani, Yoshinao Oda, Izumi Kinoshita, Kenichi Kohashi, Junkichi Takemoto, Seiichi Hirota, Akio Shibata, Tsubasa Koda, Yasuhiro Takeshima, A newborn case of jejunal ALK-negative inflammatory myofibroblastic tumor with ETV6-NTRK3 fusion, Pediatric Blood and Cancer, 10.1002/pbc.27902, 2019.01, [URL]. |
| 162. | Shinkichi Takamori, Gouji Toyokawa, Mototsugu Shimokawa, Fumihiko Kinoshita, Yuka Kozuma, Taichi Matsubara, Naoki Haratake, Takaki Akamine, Fumihiko Hirai, Tetsuzo Tagawa, Yoshinao Oda, Yoshihiko Maehara, A novel prognostic marker in patients with non-small cell lung cancer Musculo-immuno-nutritional score calculated by controlling nutritional status and creatine kinase, Journal of Thoracic Disease, 10.21037/jtd.2019.01.76, 2019.01, [URL], Background: Controlling nutritional status (CONUT) and skeletal muscle area (SMA) are both useful prognostic factors in patients with non-small cell lung cancer (NSCLC). We hypothesized that low serum creatine kinase (CK) would be a surrogate of decreased SMA, and defined a novel prognostic factor, CONUT/CK score (CNKS). The aim of this study was to elucidate the clinical significance of CNKS in NSCLC patients. Methods: One hundred and eighty-nine patients who underwent surgical resection of NSCLC and whose preoperative computed tomography images were available were enrolled. The CNKS was calculated by summing CONUT score and CK score, which was defined as 0 if the CK concentration is within normal range, and 2 if it is under lower limit. The optimal cut-off values of CNKS and CONUT score were 4 and 2, respectively. Results: Low CK was significantly associated with decreased SMA (P=0.012). The high CNKS group was significantly associated with men and smoking history (P=0.006 and P=0.015, respectively). The high CNKS group had significantly shorter overall survival (OS) and disease-free survival (DFS) (P |
| 163. | Yohei Nakashima, Takao Ohtsuka, So Nakamura, Yasuhisa Mori, Kohei Nakata, Yoshihiro Miyasaka, Kosei Ishigami, Ryota Matsuda, Yoshinao Oda, Masafumi Nakamura, Clinicopathological characteristics of non-functioning cystic pancreatic neuroendocrine tumors, Pancreatology, 10.1016/j.pan.2018.11.010, 2019.01, [URL], Background/objectives: The biological features of cystic pancreatic neuroendocrine tumors (PNETs) remain unclear. The aim of this study was to clarify the clinicopathological characteristics of non-functioning PNETs (NF-PNETs) with a cystic component. Methods: The medical records of 75 patients with NF-PNETs who had undergone resection in our institution were retrospectively reviewed. Clinicopathological factors were compared between PNETs with and without a cystic component. Expression of somatostatin 2 receptor (SSTR-2) was also analyzed. Results: Cystic PNETs were diagnosed in 14 patients (19%). The proportion of men was significantly higher for cystic than solid PNETs (79% vs. 44%, P |
| 164. | Yutaka Koga, Minako Hirahashi, Yoshihiro Ohishi, Yoshinao Oda, Clinicopathological features and phenotypic classification of de novo-type colorectal carcinomas differ from those of colorectal carcinomas derived from flat adenomas, Pathology International, 10.1111/pin.12803, 2019.01, [URL], Since adenoma components disappear with tumor progression, it is not known whether colorectal carcinomas (CRCs) are derived from an adenoma–carcinoma sequence or are de novo. We compared 38 cases of ≤10-mm flat CRCs without an adenoma component (de novo type) with 39 cases of ≤10-mm flat CRCs with an adenoma component (carcinoma in adenoma (CIA) type). Compared to the CIA type, the de novo-type CRCs were more frequently located in the proximal colon; more frequently invaded submucosa, and more frequently had venous permeation. Regarding the phenotypic classification based on the immunohistochemical expressions of CD10, MUC2 and MUC5AC, the incidence of unclassified type (CD10−, MUC2− and MUC5AC−) was significantly more frequent in the de novo (32%) than CIA (5%) type. In one de novo-type case, mismatch repair (MMR) protein loss was judged, because MLH1 and PMS2 protein expressions were immunohistochemically negative. BRAF mutation (V600E) was seen in one de novo-type case and two CIA-type cases, but none of these cases had MMR protein loss. In conclusion, small-intestinal type (CD10+ and MUC5AC−) is the most common in flat CRC and unclassified type is mainly characteristic of de novo type. In this study, small flat CRCs with BRAF mutation do not have MMR protein loss.. |
| 165. | Masato Yoshimoto, Yuichi Yamada, Shin Ishihara, Kenichi Kohashi, Yu Toda, Yoshihiro Ito, Hidetaka Yamamoto, Masutaka Furue, Yasuharu Nakashima, Yoshinao Oda, Comparative study of myxofibrosarcoma with undifferentiated pleomorphic sarcoma Histopathologic and clinicopathologic review, American Journal of Surgical Pathology, 10.1097/PAS.0000000000001389, 2019.01, [URL], Myxofibrosarcoma (MFS) is a malignant fibroblastic/ myofibroblastic neoplasm with the prominent myxoid area. It has the clinical features of frequent local recurrence and occasional distant metastasis. Morphologically, MFS is occasionally difficult to distinguish from undifferentiated pleomorphic sarcoma (UPS), especially in the case of high-grade MFS. Here, we reviewed clinical and histologic data of 162 MFS cases and 43 UPS cases. MFS was distinguished from UPS with the criterion of 10% myxoid area as a cutoff value. Overall, 52MFS (34.4%) and 9 UPS (20.9%) cases showed local recurrence, 18 MFS (12.2%) and 19 UPS (44.2%) cases developed distant metastasis, and 13 MFS (9.5%) and 14 UPS (32.6%) cases resulted in tumor-related death. Statistically, MFS had a better prognosis than UPS. Moreover, MFS with less myxoid area had a tendency to present a poorer prognosis. FNCLCC grade was a statistically significant prognostic factor (distant metastasis: P=0.0021, tumor-related death: P=0.0021). Cellularity and nuclear atypia had only a statistical tendency for associations with a poorer prognosis. The overall survival rate of MFS after transformation into a UPS-like condition ( |
| 166. | Rina Jiromaru, Hidetaka Yamamoto, Ryuji Yasumatsu, Takahiro Hongo, Yui Nozaki, Kazuki Hashimoto, Kenichi Taguchi, Muneyuki Masuda, Takashi Nakagawa, Yoshinao Oda, HPV-related Sinonasal Carcinoma Clinicopathologic Features, Diagnostic Utility of p16 and Rb Immunohistochemistry, and EGFR Copy Number Alteration, American Journal of Surgical Pathology, 10.1097/PAS.0000000000001410, 2019.01, [URL], The prevalence and prognostic value of human papillomavirus (HPV) infection and epidermal growth factor receptor (EGFR) alteration in sinonasal squamous cell carcinoma (SNSCC) are not known. The reliability of p16 overexpression as a surrogate for HPV infection in SNSCC is also unclear. We investigated the prognostic and diagnostic significances of HPV infection, EGFR alteration, and p16 expression in SNSCC. We analyzed high-risk HPV infection by HPV-RNA in situ hybridization and EGFR gene copy number gain (CNG) by chromogenic in situ hybridization and by determining the protein expressions of p16, Rb, and EGFR by immunohistochemistry in 101 SNSCC cases. HPV infection (n=9, 8.9%) and p16 overexpression (n=15, 14.9%) were associated with better overall survival (P=0.0042 and 0.005, respectively). The HPV+ cases were located predominantly at the nasal cavity with nonkeratinizing histology and partial loss of Rb. Notably, 40% (6/15) of p16+ SNSCCs were HPV-. Two of these cases showed complete loss of Rb expression by immunohistochemistry, suggesting a reason for the above discrepancy. EGFR CNG, detected in 30.5% of the SNSCCs, was correlated with EGFR protein overexpression (P=0.0001). HPV infection and EGFR CNG were mutually exclusive. The HPV+/EGFR CNG- group had significantly better overall survival than the HPV-/EGFR CNG- and HPV-/EGFR CNG+ groups (P=0.0471 and 0.0343, respectively). Our results suggest that HPV infection is a favorable prognostic marker in SNSCC, but p16 is not a perfect surrogate marker; the Rb expression pattern may improve the diagnostic accuracy. The molecular subclassification of SNSCCs based on HPV infection and EGFR copy number status might provide important information for therapeutic strategies.. |
| 167. | Hidetaka Yamamoto, Shin Ishihara, Yu Toda, Yoshinao Oda, Histone H3.3 mutation in giant cell tumor of bone an update in pathology, Medical Molecular Morphology, 10.1007/s00795-019-00238-1, 2019.01, [URL], Giant cell tumor of bone (GCTB) is a locally aggressive bone tumor that frequently shows local recurrence and occasionally shows malignant transformation to high-grade sarcoma. Histologically, conventional GCTB is composed mainly of three types of cells: mononuclear neoplastic cells with an osteoblastic precursor phenotype, mononuclear histiocytic cells, and osteoclast-like multinucleated giant cells. These cells interact with each other via the RANKL-RANK axis and other mechanisms for tumor formation. The vast majority of GCTBs were recently revealed to harbor H3F3A p.G34W mutation, and a minor subset have H3F3A p.G34L, p.G34M, p.G34R, or p.G34V mutation. H3.3 G34W mutant-specific immunohistochemistry is a highly sensitive and specific surrogate marker for H3F3A p.G34W mutation in GCTB and thus useful for differential diagnoses of histological mimics. H3.3 mutant-specific immunohistochemistry has also contributed to the understanding of the bone-forming ability of neoplastic cells of GCTB and the remarkable new bone formation after treatment with denosumab, an inhibitor of RANKL. In primary and secondary malignant GCTBs, the H3F3A gene allele can be preserved or lost with malignant transformation.. |
| 168. | Yoshihiro Miyasaka, Takao Ohtsuka, Ryuichiro Kimura, Ryota Matsuda, Yasuhisa Mori, Kohei Nakata, Daisuke Kakihara, Nao Fujimori, Takamasa Ohno, Yoshinao Oda, Masafumi Nakamura, Neoadjuvant Chemotherapy with Gemcitabine Plus Nab-Paclitaxel for Borderline Resectable Pancreatic Cancer Potentially Improves Survival and Facilitates Surgery, Annals of Surgical Oncology, 10.1245/s10434-019-07309-8, 2019.01, [URL], Background: Accumulation of evidence suggests that neoadjuvant chemotherapy improves the outcomes of borderline resectable pancreatic cancer (BRPC). Gemcitabine plus nab-paclitaxel (GnP) has been widely accepted as systemic chemotherapy for unresectable pancreatic cancer and reportedly results in remarkable tumor shrinkage. This study was performed to evaluate the safety and efficacy of neoadjuvant chemotherapy using neoadjuvant GnP for BRPC. Methods: The medical records of 57 patients who underwent treatment of BRPC from 2010 to 2017 were retrospectively reviewed. The patient characteristics and short- and intermediate-term outcomes were compared between the GnP and upfront surgery (UFS) groups. Results: The GnP group comprised 31 patients and the UFS group comprised 26 patients. The patient characteristics were comparable with the exception of a higher prevalence of arterial involvement in the GnP group. Twenty-seven of the 31 patients (87%) in the GnP group and all 26 patients in the UFS group underwent resection. The GnP group showed a significantly shorter operation time (429 vs. 509.5 min, p = 0.0068), less blood loss (760 vs. 1324 ml, p = 0.0115), and a higher R0 resection rate (100% vs. 77%, p = 0.0100) than the UFS group. Postoperative complications and hospital stay were comparable between the two groups, and no treatment-related mortality occurred in either group. Both the disease-free survival and overall survival times were significantly longer in the GnP group (p = 0.0018 and p = 0.0024, respectively). Conclusions: Neoadjuvant GnP is a safe and effective treatment strategy for BRPC. It potentially improves patients’ prognosis and facilitates surgical procedures.. |
| 169. | Takako Ito, Atsunobu Takeda, Kohta Fujiwara, Eiichi Hasegawa, Shintaro Nakao, Yoshihiro Ohishi, Yoshinao Oda, Hiroshi Yoshikawa, Koh Hei Sonoda, Risk factors for failure of vitrectomy cell block technique in cytological diagnosis of vitreoretinal lymphoma, Graefe's Archive for Clinical and Experimental Ophthalmology, 10.1007/s00417-019-04266-6, 2019.01, [URL], Purpose: To determine the factors that may affect the accuracy of vitrectomy cell block technique in detecting atypical lymphoid cells in patients with vitreoretinal lymphoma (VRL). Methods: We retrospectively reviewed 43 eyes in 39 patients who underwent vitrectomy for definitive histological diagnosis of VRL with vitrectomy cell block technique and/or smear preparation at Kyushu University Hospital from January 2001 to March 2016. The association of detection of atypical lymphoid cells using vitrectomy cell block technique with the following factors was assessed using logistic regression analysis: age at diagnosis, sex, presence or absence of concurrent cataract surgery with vitrectomy, clinical grading of vitreous haze, presence or absence of subretinal tumor infiltration, interval between initial symptoms and vitrectomy, and presence or absence of systemic corticosteroid therapy before vitrectomy. Results: Atypical lymphoid cells were more significantly detected using vitrectomy cell block technique compared to that using smear preparation (p = 0.018). After adjusting for age and sex, concurrent cataract surgery (odds ratio [OR], 10.41; 95% confidence interval [CI], 1.42–76.41) and subretinal tumor infiltration (OR, 5.06; 95% CI, 1.06–24.32) were significantly associated with failure of histological analysis with vitrectomy cell blocks. In multivariable logistic regression analysis, similar results were obtained, although subretinal tumor infiltration was only marginally associated with the detective capability of the technique. Conclusion: Vitrectomy cell block technique significantly improved the definitive diagnosis of VRL. Concurrent cataract surgery with vitrectomy and subretinal tumor infiltration were risk factors for failure in vitrectomy cell blocks.. |
| 170. | Yuka Kozuma, Gouji Toyokawa, Yuichi Yamada, Fumihiro Shoji, Koji Yamazaki, Yoshinao Oda, Sadanori Takeo, Spread through air spaces in non-small cell lung cancer, Journal of Thoracic Disease, 10.21037/jtd.2019.08.97, 2019.01, [URL]. |
| 171. | Akira Miyama, Shigeyuki Kuratsu, Satoshi Takenaka, Michiko Yoshimura, Genichiro Yoneda, Yuichi Yamada, Yoshinao Oda, Two case reports of intra-articular nodular fasciitis of the knee confirmed by MYH9-USP6 gene fusion expression, Journal of Orthopaedic Science, 10.1016/j.jos.2018.12.008, 2019.01, [URL], Aim: To describe two cases of intra-articular nodular fasciitis (NF) which developed within the knee joint and were associated with the expression of the MYH9-USP6 gene fusion. Patients and methods: Two women, 30 and 56 years of age, with no history of joint disease or knee joint trauma, are presented in our cases. We report these cases describing the clinical presentation, assessment, histopathological examination, gene expression, and clinical management. Results: Both patients presented with knee pain and limitation in the range of flexion. We diagnosed our two cases as intraarticular nodular fasciitis based on histological findings and by the detection of the MYH9-USP6 gene fusion. The transcript of MYH9-USP6 gene fusion was identified by RT-PCR and direct sequencing in both cases. Conclusion: We report the first cases of intra-articular NF involving the knee joint, with identification of a MYH9-USP6 gene fusion by RT-PCR. NF should be considered in the differential diagnosis of intra-articular lesions.. |
| 172. | Kenji Yorita, Yuki Togashi, Hideyuki Nakagawa, Katsushi Miyazaki, Seiji Sakata, Satoko Baba, Kengo Takeuchi, Yoshihiro Hayashi, Ichiro Murakami, Naoto Kuroda, Yoshinao Oda, Kenichi Kohashi, Yuichi Yamada, Daisuke Kiyozawa, Michael Michal, Michal Michal, Vocal cord inflammatory myofibroblastic tumor with mucoid deposits harboring TIMP3–ALK fusion A potential diagnostic pitfall, Pathology International, 10.1111/pin.12796, 2019.01, [URL], A 35-year-old Japanese man who had experienced hoarseness for 10 years presented with a vocal cord lesion. A gross examination revealed a left vocal cord polyp occupying two-thirds of the vocal space. The endoscopically resected lesion contained scattered atypical fibroblastic, stellate, or ganglion-like cells with mucoid stroma. Vacuolated cells were also seen. Lymphoplasmacytic infiltrate was largely undetectable. A vocal cord polyp was first suspected, but well-differentiated liposarcoma and inflammatory myofibroblastic tumor (IMT) were included in the differential diagnoses. The tumor cells were positive for anaplastic lymphoma kinase (ALK), calponin, and vimentin, and negative for other smooth muscle markers by immunohistochemistry. Structures resembling myofibroblasts were not observed by electron microscopy, which confirmed abundant rough endoplasmic reticulum in the tumor cells and accumulated lipid droplets in some tumor cells. ALK gene rearrangement was detected by fluorescence in situ hybridization, and TIMP3–ALK fusion was confirmed by 5′ rapid amplification of cDNA ends. We diagnosed the lesion as an IMT, and an ALK-rearranged stellate cell tumor may be postulated. This is the first report of a fusion partner gene of ALK in a case of laryngeal IMT.. |
| 173. | Koga N, Kubo N, Saeki H, Sasaki S, Jogo T, Hirose K, Nakashima Y, Oki E, Koga Y, Oda Y, Oiwa H, Oiwa T, Maehara Y. , Primary amelanotic malignant melanoma of the esophagus: a case report., Surg Case Rep., 2019.01. |
| 174. | 宮ヶ原 典 、藤 森 尚 、大 野 隆 真、岡本実里、 佐藤直市、 園田紀之、孝橋賢一 、 石神康生、小川佳宏 , 急性膵炎と低血糖が先行し，膵 CT 所見の経時的変化を観察しえた劇症 1 型糖尿病の 1 例, 日本消化器病学会雑誌., 2019.01. |
| 175. | Ryo Yamasaki, Tomomi Yonekawa, Saeko Inamizu, Koji Shinoda, Hirofumi Ochi, Takuya Matsushita, Noriko Isobe, Gaku Tsuji, Shoko Sadashima, Yuki Kuma, Yoshinao Oda, Toru Iwaki, Masutaka Furue, Jun ichi Kira, A case of overlapping adult-onset linear scleroderma and Parry-Romberg syndrome presenting with widespread ipsilateral neurogenic involvement, Neuropathology, 10.1111/neup.12614, 2019.01, [URL], Linear scleroderma is a variant of localized scleroderma. We report a 43-year-old woman who had developed left arm weakness and linear scleroderma on her back during pregnancy at 25 years of age, followed by left hemifacial atrophy and left leg weakness. She had multiple linear scleroderma lesions on her trunk and left limbs, left eyelid ptosis, impairment of vertical movement and abduction of the left eye, left hemifacial atrophy, and weakness and atrophy of the sternocleidomastoid, trapezius, and proximal limb muscles on the left side. On serology, antibodies to U1-ribonucleoprotein and Jo-1 were positive; anti-scleroderma-70 antibody was negative. Skin biopsy demonstrated increased hypertrophic collagen fibers without inflammatory infiltrates. Needle electromyography of left limb muscles revealed mild neurogenic patterns; left quadriceps muscle biopsy showed chronic neurogenic changes. Brain magnetic resonance imaging revealed mild left hemispheric atrophy. This is a rare case of linear scleroderma and Parry–Romberg syndrome presenting with widespread ipsilateral neurogenic manifestations.. |
| 176. | 佐内透、平木由佳、尾上友朗、福満東馬、小田義直 , 大動脈解離により死亡した長期透析患者の剖検例, 臨床雑誌内科. , 123(1):155-158, 2019.01. |
| 177. | 戸田雄、小田義直
, 骨腫瘍 類軟骨骨化を来す腫瘍と軟骨肉腫の亜型の鑑別 【画像診断】骨・軟部腫瘍の鑑別診断のポイント, 画像診断増刊号, 39(4):S22-S25, 2019.01. |
| 178. | 木村理恵、大久保文彦、山元英崇、野上美和子、中附加奈子、山口知彦、蘆田健二、安松隆治、三好圭、小田義直 , 甲状腺細胞診にて「濾胞性腫瘍」症例の後方視的検討, J.Kyushu-Okinawa Soc.Clin.Cytol, 50:35-38, 2019.01. |
| 179. | 小田義直, 悪性軟部腫瘍の病理診断, クリニシアン, 2018.12. |
| 180. | Kobayashi H, Kobayashi Y, Yuasa S, Okabe M, Yamada Y, Oda Y, Debiec-Rychter M, Rubin BP, Suzuki T. , A Case of Undifferentiated Sarcoma in the Superior Vena Cava and Bilateral Cervical Veins., Am J Case Rep., 2018.11. |
| 181. | Yugawa K, Yoshizumi T, Mano Y, Harada N, Itoh S, Ikegami T, Soejima Y, Fujita N, Kohashi K, Aishima S, Oda Y, Mori M. , Primary intrahepatic cholangiocarcinoma with sarcomatous stroma: case report and review of the literature., Surg Case Rep. , 4(1):138. , 2018.11. |
| 182. | Miyazaki T, Aishima S, Fujino M, Ozono K, Kubo Y, Ushijima Y, Osoegawa T, Ihara E, Tetsuhide I, Ohtsuka T, Nakamura M, Oda Y. , Neuroendocrine tumor of the pancreas with rhabdoid feature. , Virchows Arch. , 473(2):247-252., 2018.08. |
| 183. | Saeki K, Miyasaka Y, Ohishi Y, Yamamoto T, Matsuda R, Mochidome N, Mori Y, Nakata K, Ohtsuka T, Ishigami K, Minoda Y, Koga Y, Oda Y, Nakamura M. , Intrapancreatic recurrence of intraductal tubulopapillary neoplasm (ITPN) 16 years after the initial surgery for noninvasive ITPN: a case report. , Surg Case Rep. , 16;4(1):96. , 2018.08. |
| 184. | Jogo T, Oki E, Fujiwara M, Kurashige J, Nakanishi R, Sugiyama M, Nakashima Y, Saeki H, Tsuruta S, Nishimura M, Oda Y, Maehara Y., Non-familial juvenile polyposis of the stomach with gastric cancers: a case report. , Surg Case Rep. , 4(1):79, 2018.07. |
| 185. | 高岡雄大, 勝原俊亮, 内村浩太郎, 久保宏明, 後藤達郎, 大神吉光, 岡田泰代, 木村壽成, 森田孝一郎, 牛島泰宏, 中山宏道, 大塚隆生, 中村雅史, 持留直希, 大石善丈, 小田義直, 五十嵐久人, 伊藤鉄英
, 急性膵炎を合併した膵動静脈奇形の1例 , 膵臓, 2018.06. |
| 186. | 小田義直, 脂肪肉腫およびその鑑別を要する軟部腫瘍における免疫染色新規マーカー, 病理と臨床・別刷, 2018.06. |
| 187. | 木下伊寿美、孝橋賢一、小田義直, 肉腫 １）軟部肉腫の病理分類バイオマーカーについて, 腫瘍内科, 2018.06. |
| 188. | 藤原美奈子、保利喜史、古賀裕、森山智彦、江﨑幹宏、小田義直, 好酸球食道炎の病理診断, 胃と腸, 2018.05. |
| 189. | Kawazoe T, Saeki H, Edahiro K, Korehisa S, Taniguchi D, Kudou K, Nakanishi R, Kubo N, Ando K, Nakashima Y, Oki E, Fujiwara M, Oda Y, Maehara Y., A case of mixed adenoneuroendocrine carcinoma (MANEC) arising in Barrett's esophagus: literature and review. , Surg Case Rep. , 4(1):45., 2018.05. |
| 190. | 久野 恭子,森 泰寿,大塚 隆生,仲田 興平,小田義直,中村 雅史, 嚢胞空腸吻合術後の膵嚢胞性疾患に対し腹腔鏡下膵体尾部切除術を施行した一例, 日本内視鏡外学会雑誌, 2018.03. |
| 191. | 山田裕一、小田義直, 臨床研究論文の書き方 , 病理と臨床・別刷, 2018.03. |
| 192. | Kinoshita F, Shoji F, Takada K, Toyokawa G, Okamoto T, Yano T, Oda Y, Maehara Y.
, Mucinous adenocarcinoma of the thymus: report of a case. , Gen Thorac Cardiovasc Surg. , 2018.02. |
| 193. | Kohsaka S, Saito T, Akaike K, Suehara Y, Hayashi T, Takagi T, Kaneko K, Ueno T, Kojima S, Kohashi KI, Mano H, Oda Y, Yao T.
, Pediatric soft tissue tumor of the upper arm with LMNA-NTRK1 fusion. , Hum Pathol., 72:167-173. , 2018.02. |
| 194. | Harimoto N, Yugawa K, Ikegami T, Ohira M, Mano Y, Motomura T, Toshima T, Itoh S, Harada N, Soejima Y, Yoshizumi T, Maehara Y, Oda Y.
, Hepatobiliary and Pancreatic: Pregnancy induced hepatic veno-occlusive disease requiring liver transplantation. , J Gastroenterol Hepatol. , 33(1):9., 2018.01. |
| 195. | Kuwamoto S, Matsushita M, Takeda K, Tanaka N, Endo Y, Yamasaki A, Kohashi K, Oda Y, Horie Y.
, SMARCA4-deficient thoracic sarcoma: report of a case and insights into how to reach the diagnosis using limited samples and resources. , Hum Pathol. , 70:92-97. , 2017.12. |
| 196. | Ono M, Kasuga Y, Uehara T, Oda Y.
, Epithelioid hemangioendothelioma of the thyroid: a case report. , Surg Case Rep. , 3(1):18., 2017.12. |
| 197. | Sasaki S, Sugiyama M, Nakaji Y, Nakanishi R, Nakashima Y, Saeki H, Oki E, Oda Y, Maehara Y.
, Anal metastasis of rectal cancer-adenocarcinoma of squamous cells: a case report and literature review. , Surg Case Rep. , 2017.12. |
| 198. | Shindo K, Nagai E, Nabae T, Eguchi T, Moriyama T, Ohuchida K, Manabe T, Ohtsuka T, Oda Y, Hashizume M, Nakamura M.
, Successful video-assisted thoracoscopic surgery in prone position in patients with esophageal cancer and aberrant right subclavian artery: report of three cases. , Surg Case Rep., 3(1):86. , 2017.12. |
| 199. | Yoshiya K, Imamura Y, Nakaji Y, Taniguchi D, Takeda R, Ando K, Nakashima Y,
Shimizu M, Ohgaki K, Furusyo N, Matsumoto T, Saeki H, Oda Y, Oki E, Maehara Y.
, Successful surgical intervention for rectal perforation due to polyarteritis nodosa : report of a case. , Surg Case Rep. , 3(1):43. , 2017.12. |
| 200. | 伊達直希,庄司剛,若月悠佑,山田裕一,小田義直,片倉浩理, 肺内に発生した未分化/分類不能型肉腫の1 例, Japanese Journal of Lung Cancer, 57(7):866-869, 2017.12. |
| 201. | Yoshihiro T, Tsuchihashi K, Nio K, Arita S, Nakano T, Yasumatsu R, Jiroumaru R, Ariyama H, Kusaba H, Oda Y, Akashi K, Baba E.
, Lingual alveolar soft part sarcoma responsive to pazopanib: A case report. , Medicine (Baltimore)., 2017.11. |
| 202. | Kishida N, Sentani K, Terada H, Honda Y, Goto K, Hatanaka Y, Kohashi K, Oda Y, Iwata J, Yasui W, Shinmei S, Hayashi T, Teishima J, Matsubara A, Nakamura Y, Iida M, Awai K. , Anastomosing haemangioma with fatty changes in the perirenal space: a lesion mimicking liposarcoma, BJR Case Rep., doi: 10.1259/bjrcr.20170022. , 4(2):20170022., 2017.11. |
| 203. | Ikematsu Y, Yoneshima Y, Ijichi K, Tanaka K, Harada T, Oda Y, Nakanishi Y, Okamoto I., Marked response to pembrolizumab in a patient with pulmonary pleomorphic carcinoma highly positive for PD-L1., Lung Cancer., 112:230-231, 2017.10. |
| 204. | Okumura Y, Kohashi K, Wang H, Kato M, Maehara Y, Ogawa Y, Oda Y.
, Combined primary hepatic neuroendocrine carcinoma and hepatocellular carcinoma with aggressive biological behavior (adverse clinical course): A case report. , Pathol Res Pract. , 213(10):1322-1326., 2017.10. |
| 205. | Fujimoto Y, Nakashima Y, Sasaki S, Jogo T, Hirose K, Edahiro K, Korehisa S, Taniguchi D, Kudou K, Nakaji YU, Nakanishi R, Ando K, Saeki H, Oki E, Fujiwara M, Oda Y, Maehara Y., Chemoradiotherapy for Solitary Skeletal Muscle Metastasis from Oesophageal Cancer: Case Report and Brief Literature Review. , Anticancer Res. , 37(10):5687-5691 , 2017.10. |
| 206. | Oda Y, Yamamoto H, Kohashi K, Yamada Y, Iura K, Ishii T, Maekawa A, Bekki H., Soft tissue sarcomas: From a morphological to a molecular biological approach., Pathol Int., 67(9):435-446, 2017.09. |
| 207. | Akamine T, Toyokawa G, Kohashi K, Matsubara T, Kozuma Y, Haratake N, Takamori S, Katsura M, Takada K, Shoji F, Okamoto T, Oda Y, Maehara Y.
, Highlighted version successful resection of a tracheal metastasis of rectal cancer: a case report. , J Thorac Dis. , E797-E800. , 2017.09. |
| 208. | Tsuruta N, ,Takayoshi K, Arita S, Aikawa T , Ariyama H, Kusaba H, Ohuchida K,
Nagai E, Kohashi K, Hirahashi M, Inadomi K, Tanaka M, Sagara K, Okumura Y, Nio K, Nakano M, Nakamura M, Oda Y, Akashi K, Baba E.
, Systemic chemotherapy with pronounced efficacy and neutropenia in a granulocyte-colony stimulating factor-producing advanced gastric neuroendocrine carcinoma , Oncol Lett., 14(2):1500-1504., 2017.08. |
| 209. | 森岡友佳,辻学,伊東孝通,水江航之介,薄手政博,中原剛士,三苫千景,内博史,山田裕一,小田義直,古江増隆, 隆起性皮膚線維肉腫より生じたと考えられた線維肉腫, 西日本皮膚科別冊, 79(4):337-338, 2017.08. |
| 210. | Tanaka M, Kohashi K, Kushitani K, Yoshida M, Kurihara S, Kawashima M, Ueda Y, Souzaki R, Kinoshita Y, Oda Y, Takeshima Y, Hiyama E, Taguchi T, Tanaka Y., Inflammatory myofibroblastic tumors of the lung carrying a chimeric A2M-ALK gene: report of 2 infantile cases and review of the differential diagnosis of infantile pulmonary lesions, Hum Pathol., doi: 10.1016/j.humpath., 66:177-182. , 2017.08. |
| 211. | Hatano T, Ohishi M, Yoshimoto G, Yamauchi M, Maekawa A, Yamamoto H, Oda Y, Endo M, Bekki H, Matsunobu T, Nakashima Y, Okazaki K, Fukushi JI, Oyamada A, Iwamoto Y.
, Methotrexate-Related Lymphoproliferative Disorder Presenting with Severe Swelling of the Elbow Joint: A Case Report. , JBJS Case Connect. , 7(3):e65. , 2017.07. |
| 212. | Nishijima T, Yamamoto H, Nakano T, Hatanaka Y, Taguchi KI, Masuda M, Oda Y., Low-grade intraductal carcinoma (low-grade cribriform cystadenocarcinoma) with tumor-associated lymphoid proliferation of parotid gland., Pathol Res Pract., 213(6):706-709., 2017.06. |
| 213. | Takizawa K, Kohashi K, Negishi T, Taguchi K, Yamada Y, Nakamura M, Oda Y.
, A exceptional collision tumor of primary adrenal angiosarcoma and non-functioning adrenocortical adenoma. , Pathol Res Pract. , 213(6):702-705., 2017.06. |
| 214. | Yoshihiro T, Nio K, Tsuchihashi K, Ariyama H, Kohashi K, Tsuruta N, Hanamura F, Inadomi K, Ito M, Sagara K, Okumura Y, Nakano M, Arita S, Kusaba H, Oda Y, Akashi K, Baba E.
, Pancreatic acinar cell carcinoma presenting with panniculitis, successfully treated with FOLFIRINOX: A case report. , Mol Clin Oncol. , 6(6):866-870. , 2017.06. |
| 215. | Aso A, Ihara E, Nakamura K, Sudovykh I, Ito T, Nakamura M, Ikeda T, Takizawa N,
Oda Y, Shimizu S.
, Solid Pseudopapillary Neoplasm of the Pancreas in Young Male Patients: Three Case Reports. , Case Rep Gastrointest Med. , 2017.05. |
| 216. | Ogata H, Yamamoto Y, Harada T, Nakanishi Y, Okamoto I, Iwama E, Kato K, Oda Y., Severe Aplastic Anemia during Osimertinib Therapy in a Patient with EGFR Tyrosine Kinase Inhibitor-Resistant Non-Small Cell Lung Cancer. , J Thorac Oncol. , 12(5):e46-e47., 2017.05. |
| 217. | Tsuchihashi K, Kusaba H, Yamada Y, Okumura Y, Shimokawa H, Komoda M, Uchino K, Yoshihiro T, Tsuruta N, Hanamura F, Inadomi K, Ito M, Sagara K, Nakano M, Nio K, Arita S, Ariyama H, Kohashi K, Tominaga R, Oda Y, Akashi K, Baba E
, Programmed death-ligand 1 expression is associated with fibrosarcomatous transformation of dermatofibrosarcoma protuberans , Mol Clin Oncol. , 6(5):665-668. , 2017.05. |
| 218. | Kohashi K, Oda Y., Oncogenic roles of SMARCB1/INI1 and its deficient tumors., Cancer Sci., 108(4):547-552, 2017.04. |
| 219. | 大塚洋,小田義直, 筋骨格系 関節, 福岡医学雑誌, 108(6)別刷:163-175, 2017.04. |
| 220. | Adachi K, Umezaki T, Nishijima T, Yamamoto H, Oda Y., Long-term outcomes of type I thyroplasty with silicone implantation: Assessment of excised laryngeal tissue from a patient with secondary hypopharyngeal carcinoma. , Auris Nasus Larynx., 44(2):245-248., 2017.04. |
| 221. | 戸次大史, 小田 義直, 皮下軟部腫瘍の病理組織像の特徴と基礎知識, PEPARS, 122(別刷）:74-81, 2017.02. |
| 222. | 宮崎玲子, 内博史, 伊東孝通, 石井武彰, 山田裕一, 小田義直, 古江増隆, 脱分化型脂肪肉腫と鑑別を要した未分化多形肉腫の1例 , 西日本皮膚科, 79(1):46-47, 2017.02. |
| 223. | 宮崎玲子, 内 博史, 伊東孝通, 石井武彰, 山田裕一, 小田義直, 古江増隆 , 脱分化型脂肪肉腫と鑑別を要した未分化多形肉腫の1例 , 西日本皮膚科 , 2017Feb;79(1):46-47, 2017.02. |
| 224. | Yoshihiro T, Tsuchihashi K, Kusaba H, Nakashima T, Obara T, Nio K, Takayoshi K, Kodama H, Tsuruta N, Kiyohara H, Asai K, Harada E, Kamezaki K, Arita T, Sato M, Yamamoto H, Arita S, Ariyama H, Odashiro K, Oda Y, Akashi K, Baba E., Cardiac metastasis of squamous cell carcinoma of the thyroid gland with severe disseminated intravascular coagulation: A case report, Mol Clin Oncol ., doi: 10.3892/mco.2016.1091, 6(1):91-95. , 2017.01. |
| 225. | 吉本 昌人, 山元 英崇, 大塚 洋, 孝橋 賢一, 山田 裕一, 小田 義直, 左臀部に生じたMyxoid variant of angiomatoid fibrous histiocytomaの1例 , 診断病理 , 34(4):288-292, 2017.01. |
| 226. | 高岡雄大, 勝原俊亮, 内村浩太郎, 久保宏明, 後藤達郎, 大神吉光, 岡田泰代, 木村壽成, 森田孝一郎, 牛島泰宏, 中山宏道, 大塚隆生, 中村雅史, 持留直希, 大石善丈, 小田義直, 五十嵐久人, 伊藤鉄英, 急性膵炎を合併した膵動静脈奇形の1例 , 膵臓, 32(4): 760-766, 2017.01. |
| 227. | Suzuki T, Yasumatsu R, Nakashima T, Arita S, Yamamoto H, Nakagawa T. , Primary Ewing's Sarcoma of the Sinonasal Tract: A Case Report., Case Rep Oncol. , 2017 Jan 19;10(1):91-97, 2017.01. |
| 228. | Abe A, Manabe T, Takizawa N, Ueki T, Yamada D, Nagayoshi K, Sadakari Y, Fujita H, Nagai S, Yamamoto H, Oda Y, Nakamura M., IgG4-related sclerosing mesenteritis causing bowel obstruction: a case report. , Surg Case Rep., 2016 Dec;2(1):120, 2016.12. |
| 229. | Fujiie M, Yamamoto M, Taguchi K, Iwanaga A, Ohgaki K, Egashira A, Minami K, Toh Y, Oda Y, Okamura T. , Gastric carcinosarcoma with rhabdomyosarcomatous differentiation: a case report and review., Surg Case Rep., doi: 10.1186/s40792-016-0176-z. , 2016 Dec;2(1):52., 2016.12. |
| 230. | Mizuuchi Y, Nishihara K, Hayashi A, Tamiya S, Toyoshima S, Oda Y, Nakano T. , Perivascular epithelial cell tumor (PEComa) of the pancreas: a case report and review of previous literatures., Surg Case Rep., 2016 Dec;2(1):59, 2016.12. |
| 231. | Tsutsumi S, Saeki H, Nakashima Y, Nakaji Y, Kudou K, Tsutsumi R, Nishimura S, Akiyama S, Tajiri H, Yukaya T, Tanaka K, Nakanishi R, Sugiyama M, Ohgaki K, Sonoda H, Hirahashi M, Oki E, Morita M, Oda Y, Maehara Y. , Distant lymph node metastases caused by esophageal cancer invasion to the lamina propria: a case report., Surg Case Rep. , 2016 Dec;2(1):143, 2016.12. |
| 232. | Iguchi T, Yamagata M, Sonoda T, Yanagita K, Fukahori T, Tsujita E, Aishima S, Oda Y, Maehara Y. , Malignant transformation of hepatocellular adenoma with bone marrow metaplasia arising in glycogen storage disease type I: A case report., Mol Clin Oncol. , 2016 Nov;5(5):599-603, 2016.11. |
| 233. | Mitamura Y, Azuma S, Matsumoto D, Takada-Watanabe A, Takemoto M, Yokote K, Motoshita J, Oda Y, Furue M, Takeuchi S. , Case of sarcomatoid carcinoma occurring in a patient with Werner syndrome., J Dermatol., 2016 Nov;43(11):1362-1364, 2016.11. |
| 234. | 平橋 美奈子, 宮崎正史, 江崎幹宏, 小田 義直, 消化管Ⅱー下部消化管ー 【知っておきたい比較的稀な炎症性疾患】静脈硬化症Phlebosclerosis, 病理と臨床, 34(10):1050-1054, 2016.10. |
| 235. | Kohashi K, Tanaka Y, Kishimoto H, Yamamoto H, Yamada Y, Taguchi T, Iwamoto Y, Oda Y.
, Reclassification of rhabdoid tumor and pediatric undifferentiated/unclassified sarcoma with complete loss of SMARCB1/INI1 protein expression: three subtypes of rhabdoid tumor according to their histological features., Mod Pathol. , 2016 Oct;29(10):1232-42 , 2016.10. |
| 236. | 小田 義直, 「希少がん」としての骨・軟部腫瘍の病理診断-誌説, 整形外科, 67(9):938, 2016.08. |
| 237. | Morita M, Saeki H, Nakaji Y, Zaitsu Y, Hirahashi M, Ohguri T, Oki E, Toh Y, Oda Y, Maehara Y. , Conversion to Neuroendocrine Carcinoma from Squamous Cell Carcinoma of the Esophagus After Definitive Chemoradiotherapy., Anticancer Res., 2016 Aug;36(8):4045-9, 2016.08. |
| 238. | Wada N, Ito T, Uchi H, Nakahara T, Tsuji G, Ijichi A, Yamada Y, Oda Y, Furue M. , Superficial CD34-positive fibroblastic tumor: A new case from Japan. , J Dermatol. , 2016 Aug;43(8):934-6, 2016.08. |
| 239. | 永吉絹子、植木隆、真鍋達也、遠藤翔、永井俊太郎、梁井公輔、持留直樹、平橋美奈子、小田義直、中村雅史 , 腸管子宮内膜症に対する腹腔鏡手術の経験, 日本消化器外科学会雑誌, 2016 Aug;49(8):762-771, 2016.08. |
| 240. | 大石 善丈, 小田 義直, 子宮頸部小細胞癌の２例 , 日本臨床細胞学会九州連合会雑誌, 47:101-106, 2016.07. |
| 241. | 寺戸信芳, 仲正喜, 野上美和子, 大久保文彦, 杉島節夫, 孝橋 賢一, 山元 英崇, 久保真, 徳永えり子, 小田 義直, 多形型非浸潤性小葉癌の２例 , 日本臨床細胞学会九州連合会雑誌, 47:113-117, 2016.07. |
| 242. | 中附加奈子, 大久保文彦, 仲正喜, 矢幡秀昭, 兼城英輔, 園田顕三, 加藤聖子, 加耒恒壽, 大石 善丈, 小田 義直, 子宮頸部小細胞癌の２例 , 日本臨床細胞学会九州連合会雑誌, 47:101-106, 2016.07. |
| 243. | Inadomi K, Kumagai H, Arita S, Tsuruta N, Takayoshi K, Mishima K, Ota S, Tanaka M, Okumura Y, Sagara K, Nio K, Nakano M, Uchi H, Yamamoto H, Ariyama H, Kusaba H, Niiro H, Oda Y, Akashi K, Baba E. , Bi-cytopenia possibly induced by anti-PD-1 antibody for primary malignant melanoma of the esophagus: A case report., Medicine (Baltimore). , 2016 Jul;95(29):e4283, 2016.07. |
| 244. | 山田 裕一, 小田 義直, 軟部腫瘍：変化する疾患概念 孤立性線繊維性腫瘍と血管周皮腫, 病理と臨床, 34(6):584-589, 2016.06. |
| 245. | 山元 英崇, 小田 義直, 軟部腫瘍：変化する疾患概念 脱分化型脂肪肉腫 -概念とその拡大–, 病理と臨床, 34(6):595-599, 2016.06. |
| 246. | Tahara K, Yamashita K, Hiwatashi A, Togao O, Kikuchi K, Endo M, Otsuka H, Oda Y, Honda H., MR Imaging Findings of a Leiomyosarcoma of the Thoracic Spine: A Case ReportClin Neuroradiol , Clin Neuroradiol, doi: 10.1007/s00062-015-0420-0., 2016 Jun;26(2):229-33. , 2016.06. |
| 247. | Motomatsu Y, Oishi Y, Matsunaga S, Onitsuka H, Yamamoto H, Zaitsu E, Yamada Y, Kohashi K, Oda Y, Tominaga R. , Primary Cardiac T-Cell Lymphoma Localized in the Mitral Valve., Ann Thorac Surg., 2016 Jun;101(6):2363-5, 2016.06. |
| 248. | 井浦国生, 小田 義直, 骨軟部腫瘍. 癌の分子病理学. 病理診断から治療標的探索まで , 病理と臨床.臨時増刊号, 34:221-228, 2016.04. |
| 249. | Ito T, Kohashi K, Yamada Y, Iwasaki T, Maekawa A, Kuda M, Hoshina D, Abe R, Furue M, Oda Y. , Prognostic Significance of Forkhead Box M1 (FOXM1) Expression and Antitumor Effect of FOXM1 Inhibition in Angiosarcoma., J Cancer. , 2016 Apr 27;7(7):823-30, 2016.04. |
| 250. | Sugimoto M, Kohashi K, Itsumi M, Shiota M, Abe T, Yamada Y, Kuroiwa K, Naito S, Oda Y. , Epithelial to Mesenchymal Transition in Clear Cell Renal Cell Carcinoma with Rhabdoid Features., Pathobiology. , 2016;83(6):277-86, 2016.04. |
| 251. | 平橋 美奈子, 瀧澤延喜, 大石 善丈, 小田 義直, まれな大腸悪性腫瘍の病理診断 , 胃と腸, 51(3): 309-323 , 2016.03. |
| 252. | 井浦 国生, 小田 義直, 骨軟部腫瘍の遺伝子異常と病理診断 , 43(3):300-304, 2016.03. |
| 253. | 小田 義直, 臨床検査技師として必要な病理解剖手技について , 検査と技術, 43(12):1198-204, 2015.11. |
| 254. | 小田 義直, 軟部腫瘍の新たな疾患概念 , 病理と臨床, 33(8):905-7, 2015.08. |
| 255. | 小田 義直, 2013年軟部腫瘍の新WHO分類 , 日整会誌, 89:399-404, 2015.06. |
| 256. | 前川 啓, 小田 義直, 胞巣状軟部肉腫 病理診断クイックリファレンス , 病理と臨床臨時増刊号 vol.33 p264, 文光堂 2015年, 2015.04. |
| 257. | 前川 啓, 小田 義直, 胎児型横紋肉腫 病理診断クイックリファレンス , 病理と臨床臨時増刊号 vol.33 p265, 文光堂 2015年, 2015.04. |
| 258. | 前川 啓, 小田 義直, 類上皮肉腫 病理診断クイックリファレンス , 病理と臨床臨時増刊号 vol.33 p266, 文光堂 2015年, 2015.04. |
| 259. | 山田 裕一, 小田 義直, 診療や相談に役立つがん患者100の質問, 各論(15)軟部腫瘍 , メディカルレビュー社, 188-193, 2015.04. |
| 260. | 山田 裕一, 小田 義直, 軟部腫瘍はどんながんですか？ 軟部腫瘍はどうやって診断しますか？ 軟部腫瘍はどのように治療しますか？ , 安達洋祐 編 がん患者100の質問 メディカルレビュー社 p188-193, 2015年3月, 2015.03. |
| 261. | Shinichi Aishima, Yoshinao Oda, Pathogenesis and classification of intrahepatic cholangiocarcinoma: different characters of perihilar large duct type versus peripheral small duct type., J Hepatobiliary Pancreat Sci. 2015 Feb;22(2):94-100., 2015.02. |
| 262. | Hidetaka Yamamoto, Yoshinao Oda, Gastrointestinal stromal tumor: Recent advances in pathology and genetics., Pathol Int Jan 65: 9–18, 2015, 2015.01. |
| 263. | 山元 英崇, 小田 義直, 細胞周期とチェックポイント, 病理と臨床 32(8): 907-910, 2014., 2014.08. |
| 264. | Hidetaka Yamamoto, Yoshinao Oda, 胃腸管間質腫瘍(GIST)の遺伝子異常に基づく亜型分類と臨床的意義, 福岡医学雑誌 105 (8): 157-165, 2014, 2014.08. |
| 265. | Kataoka K, Tanaka K, Mizusawa J, Kimura A, Hiraga H, Kawai A, Tomoya Matsunobu, Matsumine A, Araki N, Yoshinao Oda, Fukuda H, Yukihide Iwamoto, Tissue Tumor Study Group of the Japan Clinical Oncology Group: A randomized phase II/III trial of perioperative chemotherapy with adriamycin plus ifosfamide vs. gemcitabine plus docetaxel for high-grade soft tissue sarcoma: Japan Clinical Oncology Group study JCOG1306. , Jpn J Clin Oncol. 2014 Aug;44(8):765-9., 2014.08. |
| 266. | Yoshitane Tsukamoto, Takahiro Watanabe, Soh Nishimoto, Masao Kakibuchi, Yuichi Yamada, Kenichi Kohashi, Yoshinao Oda, Seiichi Horita, STAT6-positive intraorbital papillary tumor: A rare variant of solitary fibrous tumor?, Pathol Res Pract. 2014 Jul;210(7):450-3., 2014.07. |
| 267. | 石井 武彰, 小田 義直, 骨・軟部の未分化肉腫いわゆるMFHの概念の変遷, 臨床画像 30(7): 724-729, 2014., 2014.07. |
| 268. | 小田 義直, 紡錘形細胞軟部肉腫における細胞内シグナル伝達, 病理と臨床 32(7): 804-806, 2014, 2014.07. |
| 269. | Shohei Yoshiya, ikegami Toru, Tomoharu Yoshizumi, Huanlin Wang, Noboru Harada, Yo-ichi Yamashita, Akihiro Nishie, Ken Shirabe, Yoshinao Oda, Yoshihiko Maehara, Fairly rare de Novo inflammatory pseudotumor in a graft after living donor liver transplantation., Liver Transpl, 2014 May;20(5):616-8. , 2014.05. |
| 270. | Yasunori Sakai, Ryota Souzaki, Hidetaka Yamamoto, Yuki Matsushita, Hazumu Nagata, Ishizaki Yoshito, Hiroyuki Torisu, Yoshinao Oda, tomoaki taguchi, Chad A Shaw, Toshiro Hara, Testicular sex cord-stromal tumor in a boy with 2q37 deletion syndrome., BMC Med Genomics. 2014 Apr 22;7(1):19., 2014.04. |
| 271. | Yuka Hotokebuchi, Kenichi Kohashi, Satoshi Toyoshima, Naoko Matsumoto, Toshinori Nakashima, Yoshinao Oda, Congenital peribronchial myofibroblastic tumor., Pathol Int. 2014 Apr;64(4):189-91., 2014.04. |
| 272. | Takamichi Ito, Itoh Eriko, Ayami Koda-Maeda, Hiroaro Kiryu, Yuichi Yamada, Toshiharu Yamashita, Yoshinao Oda, Masutaka Furue, Lipoblastomatosis on the sole showing spontaneous regression., 2014.04. |
| 273. | Yusuke Inatomi, Takamichi Ito, Konosuke Nagae, Yuichi Yamada, Mari Kiyomatsu, Nakano Misa, Uchi Hiroshi, Yoshinao Oda, Masutaka Furue, Hybrid perineurioma-neurofibroma in a patient with neurofibromatosis type 1, clinically mimicking malignant peripheral nerve sheath tumor., 2014.04. |
| 274. | Harimoto Norifumi, ikegami Toru, H Nakagawara, Yo-ichi Yamashita, Tomoharu Yoshizumi, Hideaki Uchiyama, T Soejima, K Ikeda, Ken Shirabe, Shinichi Aishima, Yoshinao Oda, Yoshihiko Maehara, Chronic Immune-Mediated Reaction Syndrome as the Cause of Late Graft Mortality in Living-Donor Liver Transplantation for Primary Biliary Cirrhosis., Transplant Proc. 2014 May 14, 2014.04. |
| 275. | 山田 裕一, 小田 義直, 皮膚特有の間葉系腫瘍２：線維・線維組織球性、脂肪性およびその他の腫瘍 皮膚疾患のみかたII―腫瘍および腫瘍類似病変―, 病理と臨床 32(4): 391-399, 2014. , 2014.04. |
| 276. | 山元 英崇, 小田 義直, 細胞周期、細胞増殖からみた悪性度診断 病理と臨床 臨時増刊号 vol.32 p395-399, 2014 , 病理と臨床 臨時増刊号 vol.32 p395-399, 2014 , 2014.04. |
| 277. | H Kimura, Ohtsuka Takao, Hiroki Toma, JUNJI UEDA, Yuusuke Mizuuchi, Hidetaka Yamamoto, Shunichi Takahata, Yoshinao Oda, Takashi Ueki, Masao Tanaka, A Case of Gastrointestinal Stromal Tumor of the Jejunum Successfully Treated by Preoperative Induction Chemotherapy with Imatinib Mesylate Administered through Jejunostomy and Subsequent Surgical Resection., Gan To Kagaku Ryoho. 2014 Mar;41(3):391-4., 2014.03. |
| 278. | 蔵原 晃一, 大城 由美, 岡本 康治, 川崎 啓祐, 河内 修司, 八坂 弘樹, 鷲尾 恵万, 永田 豊, 平橋 美奈子, 江崎 幹宏, 小田 義直, 松本 主之, 渕上 忠彦, 消化管アミロイド―シスの臨床像. 画像診断を中心にーアミロイド―シスの小腸病変の特徴. , 胃と腸 49(3): 311-319, 2014, 2014.03. |
| 279. | Yuusuke Mizuuchi, Shinichi Aishima, Masami Hattori, Yasuhiro Ushijima, Akira Aso, Shunichi Takahata, Ohtsuka Takao, JUNJI UEDA, Masao Tanaka, Yoshinao Oda, Follicular pancreatitis mimicking pancreatic cancer, report of a case and review of the literature., Pathol Res Pract. 2014 Feb;210(2):118-22. (corresponding), 2014.02. |
| 280. | 髙橋 祐介, 孝橋 賢一, 小田 義直, WHO分類改訂に基づく最近の知見 , 病理と臨床 32(2): 128-132, 2014 , 2014.02. |
| 281. | Yoshihiro Matsumoto, Yusuke Takahashi, Akihisa Haraguchi, Tatsuro Okamoto, Katsumi Harimaya, Tomoya Matsunobu, Makoto Endo, Yoshinao Oda, Yukihide Iwamoto, Intraosseous hemangioma arising in the clavicle., Skeletal Radiol. 2014 Jan;43(1):89-93., 2014.01. |
| 282. | 安蘇 鉄平, 大塚 隆生, 木村 英世, 松永 壮人, 渡邊 雄介, 田村 公二, 井手野 昇, 大内田 研宙, 上田 純二, 髙畑 俊一, 相島 慎一, 五十嵐 久人, 伊藤 鉄英, 小田 義直, 水元 一博, 田中 雅夫, 膵液細胞診および膵液遺伝子検査による膵癌診断 , 臨床外科 69(1): 12-16, 2014, 2014.01. |
| 283. | Shinichi Aishima, Yuichiro Kubo, Yuki Tanaka, Yoshinao Oda, Histological features of precancerous and early cancerous lesions of biliary tract carcinoma., Journal of Hepato-Biliary-Pancreatic Sciences, 2014 Jan 21, 2014.01. |
| 284. | Makoto Endo, Hidetaka Yamamoto, Katsumi Harimaya, Kenichi Kohashi, Takeaki Ishii, N Setsu, Yukihide Iwamoto, Yoshinao Oda, Conventional spindle cell type malignant peripheral nerve sheath tumor arising in a sporadic schwannoma., Hum Pathol. 2013 Dec;44(12):2845-8. (corresponding) , 2013.12. |
| 285. | 平橋 美奈子, 小林 広幸, 恒吉 正澄, 古賀 裕, 熊谷 玲子, 長田 美佳子, 熊谷 好晃, 河野 由紀子, 髙橋 俊介, 瀧澤 延喜, 一瀬 理沙, 小田 義直, 好酸球性消化管疾患の病理―主題：好酸球性消化管疾患の概念, 2013.12. |
| 286. | Makoto Endo, Kenichi Kohashi, Hidetaka Yamamoto, Takeaki Ishii, Tatsuya Yoshida, Tomoya Matsunobu, Yukihide Iwamoto, Yoshinao Oda, Ossifying fibromyxoid tumor presenting EP400-PHF1 fusion gene. , Hum Pathol Nov;44(11):2603-2608, 2013 (corresponding), 2013.11. |
| 287. | 田村 公二, 大塚 隆生, 上田 純二, 髙畑 俊一, 小田 義直, 水元 一博, 田中 雅夫, 漿液性嚢胞腫瘍(SCN) -手術適応はどこにあるか- , 肝胆膵 67(5): 739-746, 2013., 2013.11. |
| 288. | Koji Shindo, JUNJI UEDA, Shinichi Aishima, Akira Aso, Ohtsuka Takao, Shunichi Takahata, Kousei Ishigami, Yoshinao Oda, Masao Tanaka, Small-sized, flat-type invasive branch duct intraductal papillary mucinous neoplasm: a case report., 2013.10. |
| 289. | 渡邊 祐介, 大塚 隆生, 田村 公二, 木村 英世, 松永 壮人, 井出野 昇, 安蘇 鉄平, 上田 純二, 髙畑 俊一, 牛島 泰宏, 伊藤 鉄平, 水内 祐介, 相島 慎一, 小田 義直, 水元 一博, 田中 雅夫, IPMN: 術前画像診断のポイントと術中解剖認識 IV 肝・胆・膵 , 臨床外科 68(11): 228-234, 2013, 2013.10. |
| 290. | Shinji Okano, Hidetaka Yamamoto, Shinji Kono, Hiroshi Fujii, Ken Shirabe, Yoshihiko Maehara, Yoshinao Oda, Dedifferentiated liposarcoma of a spermatic cord with a hemangioendothelioma-like component: A case report and review of the literature., Pathol Res Pract Sep;209(9):596-604, 2013 , 2013.09. |
| 291. | Yusuke Mizuuchi, Hidetaka Yamamoto, Katsuya Nakamura, Shirahane Kengo, Masae Souzaki, Masao Tanaka, Yoshinao Oda, Solitary fibrous tumor of the thyroid gland., 2013.09. |
| 292. | SATOSHI YAMASAKI, Tsuyoshi Muta, Taiki Higo, Hirotake Kusumoto, Eiko Zaitsu, Toshihiro Miyamoto, Yoshinao Oda, koichi akashi, Ventricular fibrillation after bortezomib therapy in a patient with systemic amyloidosis., Hematol Rep. 2013 Sep 16;5(3):e12. doi: 10.4081/hr.2013.e12., 2013.09. |
| 293. | 平橋 美奈子, 山元 英崇, 小田 義直, 小腸悪性腫瘍の病理学的特徴：悪性リンパ腫 , 胃と腸 48(10): 1417-1427, 2013, 2013.09. |
| 294. | Koji Tamura, Ohtsuka Takao, Noboru Ideno, Teppei Aso, Hiroshi Kono, Yousuke Nagayoshi, Koji Shindo, Yasuhiro Ushijima, JUNJI UEDA, Shunichi Takahata, Tetsuhide Ito, Yoshinao Oda, Mizumoto Kazuhiro, Masao Tanaka, Unresectable Pancreatic Ductal Adenocarcinoma in the Remnant Pancreas Diagnosed during Every-6-Month Surveillance after Resection of Branch Duct Intraductal Papillary Mucinous Neoplasm: A Case Report., J Pancreas. 2013 Jul 10;14(4):450-453. doi: 10.6092/1590-8577/1494. , 2013.07. |
| 295. | Masaki Fujioka, kenji Hayashida, Chikako Murakami, Masanori Hisaoka, Yoshinao Oda, Masahiro Ito, Cutaneous malignant rhabdoid tumor in the palm of an adult., Rare Tumors 2013-07-12 17:44:12 | DOI: 10.4081/rt.2013.e36 | , 2013.07. |
| 296. | Makoto Endo, Tatsuya Yoshida, Hidetaka Yamamoto, Takeaki Ishii, Nokitaka Setsu, Kenichi Kohashi, Tomoya Matsunobu, Yukihide Iwamoto, Yoshinao Oda, Low-grade osteosarcoma arising from bone infarct. , Hum Pathol Jun;44(6):1184-1189,2013(corresponding), 2013.06. |
| 297. | Koji Shindo, JUNJI UEDA, Taro Toubo, Masafumi Nakamura, Yoshinao Oda, Toru Eguchi, Masao Tanaka, Primary carcinoid tumor in a retroperitoneal mature teratoma: report of a case. , Surg Today. 2013 Jun;43(6):694-7., 2013.06. |
| 298. | Tsuyoshi Miyazaki, Kenzo Uchida, Takafumi Yayama, Hideaki Nakajima, Kazuya Honjoh, Hiroshi Ito, Yoshinao Oda, Hisatoshi Baba, Chondroblastoma of the distal femur resected through a small fenestra via computed tomography navigation and endoscopy: a case report., J Med Case Rep. 2013 Jun 27;7(1):164. , 2013.06. |
| 299. | 遠藤 誠, 小田 義直, 肉腫と融合遺伝子 特集：固形腫瘍と融合遺伝子, 2013.06. |
| 300. | 小田 義直, 骨・軟部腫瘍外科医と病理医のコミュニケーション , 日本整形外科学会雑誌 86(5): 420-426, 2012, 2013.05. |
| 301. | H Tsubouchi, Shunsuke Endo, Yoshinao Oda, Yoh Dobashi, Carcinoid tumor of the lung with massive ossification: report of a case showing the evidence of osteomimicry and review of the literature , Int J Clin Exp Pathol Apr 15;6(5):957-61, 2013, 2013.05. |
| 302. | 新野 大介, 山元 英崇, 宮原 司, 園田 美穂, 佐土原 順子, 小田 義直, 大島 孝一, 陰嚢内に生じた粘液型脂肪肉腫の1例 , 2013.04. |
| 303. | 髙橋 祐介, 孝橋 賢一, 山元 英崇, 松田 秀一, 岩本 幸英, 小田 義直, 肺転移を生じた軟部原発 malignant mixed tumor/ myoepithelioma の1例 , 診断病理 30(2): 154-157, 2013 , 2013.04. |
| 304. | 今村 紘子, 大石 善丈, 矢幡 秀昭, 小林 裕明, 加藤 聖子, 小田 義直, 卵巣原発肺型小細胞癌の1例, 診断病理 30(2): 158-162, 2013 , 2013.04. |
| 305. | Yusuke Takahashi, Yoshinao Oda, Hidetaka Yamamoto, Takeaki Ishii, Nokitaka Setsu, Makoto Endo, Shuichi Matsuda, Yukihide Iwamoto, Fibrocartilaginous mesenchymoma arising in the pubic bone: A case report , Pathol Int 63(4): 226-229, 2013 (corresponding) , 2013.04. |
| 306. | 山元 英崇, 小田 義直, 悪性軟部腫瘍におけるシグナル伝達因子異常の病理学的研究 Current organ topics: 骨・軟部腫瘍 , 癌と化学療法 40(3): 314-317, 2013, 2013.03. |
| 307. | 相島 慎一, 小田 義直, 発生部位からみた胆管癌の特徴 胆膵病理I: 胆道・膵臓腫瘍 update , 病理と臨床 31(3): 230-236, 2013, 2013.03. |
| 308. | Yoshihiro Matsumoto, Yusuke Takahashi, Katsumi Harimaya, NAKAGAWA Takeshi, Kenichi Kawaguchi, Seiji Okada, Hayashida Mitsumasa, Toshio Doi, Akio Sakamoto, Tomoya Matsunobu, Yoshinao Oda, Yukihide Iwamoto, Dedifferentiated chondrosarcoma of the cervical spine: a case report. , World J Surg Oncol. Feb 2;11(1):32, 2013. , 2013.02. |
| 309. | 大久保文彦, 小田 義直, 大久保文彦、麻生暁、相島慎一、小田義直 EUS（超音波内視鏡検査）による細胞診の標本作製方法 , MEDICAL TECHNOLOGY 41(1): 80-86, 2013, 2013.01. |
| 310. | 吉河康二, 田中 浩正, 篠崎 智子, 角沖 久夫, 吉田 祥子, 井上 貴史, 大石 善丈, 小田 義直, セルトリ・ライディッヒ細胞腫に酷似する組織像を呈した卵巣類内膜腺癌の１例. , 診断病理 30(1); 32-36, 2013, 2013.01. |
| 311. | N Watanabe, Katsunori Nenohi, Keisuke Takeuchi, Hiroshi Hasegawa, Tsuyoshi Tanaka, Makoto Shimomura, Kanji Tanigawa, Hajime Yokoi, Hiroshi Nakabayashi, Yoshinao Oda, A case of duodenal epithelioid hemangioma causing gastrointestinal bleeding. , Nihon Shokakibyo Gakkai Zasshi. 2012;109(12):2058-65., 2012.12. |
| 312. | Akio Sakamoto, Takeaki Ishii, Yoshinao Oda, Yukihide Iwamoto, Nonossifying fibroma presenting as an aneurysmal bone cyst: a case report, J Med Case Rep. 2012 Nov 29;6(1):407. , 2012.11. |
| 313. | Akio Sakamoto, Yoshiaki Fukutoku, Yoshihiro Matsumoto, Katsumi Harimaya, Yoshinao Oda, Yukihide Iwamoto, Myxoid liposarcoma with negative features on bone scan and [18F]-2-fluoro-2-deoxy-D-glucose-positron emission tomography., World J Surg Oncol. 2012 Oct 9;10(1):214., 2012.10. |
| 314. | 熊谷玲子, 小田 義直, 熊谷玲子、大屋正文、大島孝一、藤田綾、小田義直: 組織球様形態を示し形質細胞への分化を伴う肺MALTomaの１例 , 診断病理 29(3): 211-214, 2012, 2012.09. |
| 315. | 野上美和子, 小田 義直, 野上美和子、大久保文彦、高山浩一、矢野篤次郎、古賀孝臣、小田義直: 肺癌における細胞診の組織型推定の評価 , 日本臨床細胞学会九州連合会雑誌第43号: 57-63, 2012, 2012.07. |
| 316. | 小田 義直, 軟部肉腫における分子基盤と診断・治療 , 病理と臨床 30(7): 796-798, 2012, 2012.07. |
| 317. | Kohashi K, Takahashi Y, Taguchi T, Oda Y, Pediatric Rhabdomyosarcoma: Role of Cell Cycle Regulators Alteration M.A. Hayat (ed.), Teratoid/Rhabdoid, Brain Tumors, and Glioma, Pediatric Cancer 2, , © Springer 2012, in press (Corresponding) , 2012.05. |
| 318. | Matsumoto Y, Fujiwara T, Imamura R, Okada Y, Harimaya K, Doi T , Kawaguchi K, Okada S, Yamada Y, Oda Y, Iwamoto Y, Hematoma of the ligamentum flavum in the thoracic spine: report of two cases and possible role of the transforming growth factor beta-vascular endothelial growth factor signaling axis in its pathogenesis. , J Orthop Sci, in press, 2012.05. |
| 319. | Iida KI, Fukushi JI, Fujiwara T, Oda Y, Iwamoto Y:, Adult hypophosphatasia with painful periarticular calcification treated with surgical resection. , J Bone Miner Metab. 2011 Dec 15. [Epub ahead of print], in press, 2012.05. |
| 320. | Ishii T, Sakamoto A, Matsuda S, Matsumoto Y, Harimaya K, Takahashi Y, Oda Y, Iwamoto Y, Leiomyosarcoma in the humerus with leukocytosis and elevation of serum G-CSF. , Skeletal Radiol. 2011 Dec 14. [Epub ahead of print], in press, 2012.05. |
| 321. | 遠藤誠、小田義直、恒吉正澄, 結節性筋膜炎と悪性線維性組織球腫(MFH)との病理組織学的鑑別点 古江増隆 総編集 エキスパートに学ぶ皮膚病理診断学 , 中山書店、2012年、pp470-473, 2012.05. |
| 322. | 薛宇孝、小田義直、恒吉正澄, 皮膚・皮下平滑筋肉腫の病理組織学的特徴と鑑別診断 古江増隆 総編集 エキスパートに学ぶ皮膚病理診断学 , 中山書店、2012年、pp474-477, 2012.05. |
| 323. | 田中伸哉, 小田 義直, 腫瘍 深山正久編. はじめの一歩のイラスト病理学 , 羊土社、2012年、pp142-163, 2012.04. |
| 324. | 孝橋賢一、小田義直, 骨軟部腫瘍 がんの分子病理診断- 免疫染色と遺伝子診断の進歩 , 最新医学 67(3) 437-444, 2012 , 2012.03. |
| 325. | Anami A, Fukushima K, Fujita Y, Sato S, Matsumoto E, Endo M, Oda Y, Wake N, An antenatally diagnosed congenital orbital teratoma in which rupture was associated with intrauterine fetal death – a case report. , J Obstet Gynaecol Res Mar;38(3):578-81, 2012, 2012.03. |
| 326. | 山元英崇、小田義直, 炎症性筋線維芽細胞性腫瘍とその周辺疾患 特集 軟部腫瘍II―病理診断と最近の話題― , 病理と臨床 30(3): 258 -264 2012, 2012.03. |
| 327. | 孝橋賢一、小田義直, 上皮様軟部肉腫の鑑別診断 軟部腫瘍I –診断と研究の進歩- , 病理と臨床 30(2): 154-159, 2012, 2012.02. |
| 328. | 小田義直, 紡錘形細胞性軟部腫瘍の鑑別診断 軟部腫瘍I –診断と研究の進歩- , 病理と臨床 30(2): 168-178, 2012, 2012.02. |
| 329. | 藤野稔、大石善丈、阿萬紫、栗原秀一、上岡陽亮、恒吉正澄、小田義直, 成熟奇形腫と卵巣偽粘液腫を伴う粘液性嚢胞性腫瘍の1例 , 診断病理 29(1): 53-57, 2012, 2012.01. |
| 330. | 中島収、小田義直、飯島尋子: 坂元亨宇 座長, 座談会：肝細胞癌病理診断の現状と展望 , The Liver Cancer Journal 4(1): 15-26, 2012, 2012.01. |
| 331. | Yamada Y, Yamamoto H, Ohishi Y, Nishiyama K, Fukuhara M, Saitou T, Tsuneyoshi M, Oda Y, Sclerosing variant of perivascular epithelioid cell tumor in the female genital organs. , Pathol Int 61(12) Dec; 768–772, 2011, 2011.12. |
| 332. | 竹内正久、大石善丈、村上知彦、仲池隆史、小田義直, 後腹膜を原発とする粘液性腺癌の1例 , 診断病理 28(4) Dec: 257-260, 2011, 2011.12. |
| 333. | 山田裕一、小田義直, 結節性筋膜炎 –その病態と軟部腫瘍との鑑別点- , 整形・災害外科 54(10): 1235-1241, 2011, 2011.10. |
| 334. | Mano Y, Aishima S, Fujita N, Taketomi A, Shirabe K, Maehara Y, Oda Y, Cystic tumors of the liver; on the problems of diagnostic criteria. , Pathol Res Pract Oct 15;207(10):659-63, 2011, 2011.10. |
| 335. | 平橋美奈子、小田義直, 若年者胃癌の特徴：中高年に認める胃癌との相違―病理の立場から , 胃と腸 46(9): 1308-1315, 2011, 2011.09. |
| 336. | 小田義直, 小田義直 軟部多形性悪性腫瘍の病理診断 外科病理診断の手引 , 外科病理診断の手引 国立がん研究センターがん対策情報センター2011. 9. 27. https://preview-ganjoho.ncc.go.jp/professional/med_info/surgical_pathology/soft_tissue_pleomorphic_tumor.html , 2011.09. |
| 337. | 平橋美奈子、大城由美、松本主之、小田義直, 胃炎の生検診断―生検でわかること、わかるべきことー 消化管の病理I-上部消化管- , 病理と臨床 29(9): 952-959, 2011, 2011.09. |
| 338. | 山本卓明、小田義直, 大腿骨頭軟骨下脆弱性骨折、特発性大腿骨頭壊死、股関節唇損傷 青木隆敏編集 病理像・関節鏡像との対比と参考症例に学ぶ骨軟部の画像診断 , ベクトルコア社、東京、pp172-177, 2011, 2011.08. |
| 339. | 熊谷玲子、黒木綾、宮久禎、西山尚子、植山雅彦、伏見文良、田口健一、西山憲一、衛藤貴子、小田義直, 子宮原発が疑われた骨盤内Ewing sarcoma/ Primitive neuroectodermal tumor (PNET)の一例 , 日本臨床細胞学会九州連合会雑誌第42号: 103-107, 2011, 2011.08. |
| 340. | 小田義直, CD34（腫瘍等）解説編、診断編: 病理診断に役立つ分子生物学 , 病理と臨床 臨時増刊号 Vol. 29, 146-151, 2011, 2011.04. |
| 341. | 小田義直, 軟部肉腫の組織学的悪性度評価 長谷川匡、小田義直 編集 軟部腫瘍. 腫瘍病理鑑別診断アトラス , 文光堂、東京、pp210-214, 2011. 4 .1, 2011.04. |
| 342. | 小田義直, 上皮様肉腫 長谷川匡、小田義直 編集 軟部腫瘍. 腫瘍病理鑑別診断アトラス , 文光堂、東京、pp191-196, 2011. 4 .1, 2011.04. |
| 343. | 仲正喜、大久保文彦、渡辺寿美子、田宮貞史、加来恒壽、杉島節夫、山元英崇、小林裕明、小田義直, 子宮頚部細胞診におけるfiber cellの意義 , 日本臨床細胞学会雑誌 50(4): 209-213, 2011, 2011.04. |
| 344. | Kubota K, Okada S, Maeda T, Matsumoto Y, Sakamoto A, Harimaya K, Saiwai H, Kumamaru H, Oda Y, Iwamoto Y, Extradural nodular fasciitis arising in the spinal canal. , Spine, in press, 2011.03. |
| 345. | Sakamoto A, Imamura S, Matsumoto Y, Harimaya K, Mastuda S, Takahashi Y, Oda Y, Iwamoto Y, Bizarre parosteal osteochondromatous proliferation with an inversion of chromosome 7 , Skeletal Radiol, in press, 2011.03. |
| 346. | Souzaki R, Kinoshita Y, Matsuura T, Tajiri T, Taguchi T, Ieiri S, Hong J, Uemura M, Konishi K, Tomikawa M, Tanoue K, Hashizume M, Koga Y, Suminoe A, Hara T, Kohashi K, Oda Y, Successful resection of an undifferentiated sarcoma in a child using a real-time. Surgical navigation system in an open magnetic resonance imaging operation room. , J Periatr Surg 46(3): 608-611, 2011, 2011.03. |
| 347. | Hashimoto K, Yamamoto H, Nakano T, Oyama M, Shiratsuchi H, Nakashima T, Tamiya S, Komune S, Oda Y, Tumor-to-tumor metastasis: Lung adenocarcinoma metastatic to follicular variant of papillary thyroid carcinoma-Report of a case with pathological, immunohistochemical and molecular analyses of the different tumor cell populations. , Pathol Int, in press, 2011.03. |
| 348. | Yamamoto Y; Toyozawa S; Uede K; Oda Y, Nakamura Y; Furukawa F, Clinical and pathological changes in a long-term follow-up case of dermatofibrosarcoma protuberans. , J Dermatol 38(2); 203-205, 2011, 2011.02. |
| 349. | 小田義直, 骨軟部腫瘍の悪性転化とその分子メカニズム , 福岡医学雑誌 102(1): 1-7, 2011, 2011.01. |
| 350. | 小田義直、岩間祐基、武内章彦、土屋弘行, 骨外性Ewing肉腫/PNET 大塚隆信、福田国彦、小田義直 編集：骨・軟部腫瘍：臨床・画像・病理 , 診断と治療社、東京、pp254-255, 2011.1.11, 2011.01. |
| 351. | 小田義直、福田国彦、大塚隆信, 神経鞘腫 大塚隆信、福田国彦、小田義直 編集：骨・軟部腫瘍：臨床・画像・病理 , 診断と治療社、東京、pp222-225, 2011.1.11, 2011.01. |
| 352. | 小田義直、小山雅司、大塚隆信, メロレオストーシス 大塚隆信、福田国彦、小田義直 編集：骨・軟部腫瘍：臨床・画像・病理 , 診断と治療社、東京、pp170-171, 2011.1.11, 2011.01. |
| 353. | 石田剛、小田義直、福田国彦、大塚隆信, Florid reactive periostitis/ 手指線維骨性偽腫瘍 大塚隆信、福田国彦、小田義直 編集：骨・軟部腫瘍：臨床・画像・病理 , 診断と治療社、東京、pp164-165, 2011.1.11, 2011.01. |
| 354. | 小田義直、福庭栄治、大塚隆信, 修復性巨細胞肉芽腫 大塚隆信、福田国彦、小田義直 編集：骨・軟部腫瘍：臨床・画像・病理 , 診断と治療社、東京、pp162-163, 2011.1.11, 2011.01. |
| 355. | 小田義直、福庭栄治、大塚隆信, 褐色腫 大塚隆信、福田国彦、小田義直 編集：骨・軟部腫瘍：臨床・画像・病理 , 診断と治療社、東京、pp160-161, 2011.1.11, 2011.01. |
| 356. | 小田義直、福庭栄治、大塚隆信, 骨幹端線維性欠損 大塚隆信、福田国彦、小田義直 編集：骨・軟部腫瘍：臨床・画像・病理 , 診断と治療社、東京、pp158-159, 2011.1.11, 2011.01. |
| 357. | 小田義直、福庭栄治、大塚隆信, 骨内ガングリオン 大塚隆信、福田国彦、小田義直 編集：骨・軟部腫瘍：臨床・画像・病理 , 診断と治療社、東京、pp156-157, 2011.1.11, 2011.01. |
| 358. | 小田義直、福庭栄治、大塚隆信, Langerhans細胞組織球症 大塚隆信、福田国彦、小田義直 編集：骨・軟部腫瘍：臨床・画像・病理 , 診断と治療社、東京、pp154-155, 2011.1.11, 2011.01. |
| 359. | 小田義直、福田国彦、大塚隆信, 線維性骨異形成 大塚隆信、福田国彦、小田義直 編集：骨・軟部腫瘍：臨床・画像・病理 , 診断と治療社、東京、pp148-151, 2011.1.11, 2011.01. |
| 360. | 小田義直、高尾正一郎、大塚隆信, 骨内脂肪腫 大塚隆信、福田国彦、小田義直 編集：骨・軟部腫瘍：臨床・画像・病理 , 診断と治療社、東京、pp140-141, 2011.1.11, 2011.01. |
| 361. | 小田義直、青木隆敏、大塚隆信, 骨巨細胞腫 大塚隆信、福田国彦、小田義直 編集：骨・軟部腫瘍：臨床・画像・病理 , 診断と治療社、東京、pp126-129, 2011.1.11, 2011.01. |
| 362. | 小田義直、青木隆俊、武内章彦、土屋弘行, Ewing肉腫/PNET 大塚隆信、福田国彦、小田義直 編集：骨・軟部腫瘍：臨床・画像・病理 , 診断と治療社、東京、pp120-121, 2011.1.11, 2011.01. |
| 363. | 小田義直, 腫瘍の分類とその変遷 大塚隆信、福田国彦、小田義直 編集：骨・軟部腫瘍：臨床・画像・病理 , 診断と治療社、東京、pp54-61, 2011.1.11, 2011.01. |
| 364. | 小田義直, 生検、免疫組織化学染色と遺伝子診断 大塚隆信、福田国彦、小田義直 編集：骨・軟部腫瘍：臨床・画像・病理 , 診断と治療社、東京、pp62-68, 2011.1.11, 2011.01. |
| 365. | 小田義直, 腫瘍の分類とその変遷 大塚隆信、福田国彦、小田義直 編集：骨・軟部腫瘍：臨床・画像・病理 , 診断と治療社、東京、pp54-61, 2011.1.11, 2011.01. |
| 366. | Yokouchi Y,Hiruta N, Oharaseki T, Ihara F, Oda Y, Ito S, Yamashita H, Ozaki S, Gomi T, Takahashi K, Primary cardiac synovial sarcoma: A case report and literature review , Pathol Int 61(1): 150-155, 2011, 2011.01. |
| 367. | 小田義直, 整形外科医と病理医の連携. 中村耕三、吉川秀樹 編 整形外科パサージュ６ 軟部腫瘍プラクティガイド, 中山書店、東京, pp82-89, 2010, 2010.12. |
| 368. | 小田義直、的野浩士、松浦傑、恒吉正澄、長谷川匡、野島孝之、岩本幸英, 生検標本による軟部肉腫の組織型・悪性度判定における病理診断の問題点 , 日本整形外科学会雑誌 84(12): 1114-1119, 2010, 2010.12. |
| 369. | Tajiri T, Souzaki R, Kinoshita Y, Tanaka S, Koga Y, Suminoe A, Hara T, Kohashi K, Oda Y, Masumoto K, Ohira M, Nakagawara A, Taguchi T, Concordance for neuroblastoma in monozygotic twins: case report and review of the literature. , J Pediatr Surg 45(12): 2312-6, 2010, 2010.12. |
| 370. | Ogino T, Ueda J, Sato N, Takahata S, Mizumoto K, Nakamura M, Oda Y, Tanaka M, Repeated pancreatectomy for recurrent pancreatic carcinoma after pylorus-preserving pancreatoduodenectomy: Report of two patients. , Case Rep Gastroenterol. 2010 Oct 9;4(3):429-434, 2010.10. |
| 371. | Souzaki R, Tajiri T, Kinoshita Y, Tanaka S, Koga Y, Suminoe A, Hara T, Kohashi K, Oda Y, Taguchi T, Successful treatment of advanced pancreatoblastoma by a pylorus-preserving pancreatoduodenectomy after radiation and high-dose chemotherapy. , Pediatr Surg Int. 26(10): 1045-1048, 2010 , 2010.10. |
| 372. | 遠藤誠、小田義直, 滑膜肉腫の臨床病理-臨床病理における最近の進歩 , 整形外科 61(8): 777-782, 2010, 2010.08. |
| 373. | 小田義直, 骨外性粘液型軟骨肉腫: 整形外科医が知っておくべき骨・軟部腫瘍の組織像 , 整形外科 61(7): 670-571, 2010, 2010.07. |
| 374. | 小田義直, 平滑筋肉腫：整形外科医が知っておくべき骨・軟部腫瘍の組織像 , 整形外科 61(6): 570-571, 2010, 2010.06. |
| 375. | 小田義直, 良性骨腫瘍および腫瘍類似病変 , 今日の整形外科治療方針 第6版 医学書院 p222-225, 2010, 2010.06. |
| 376. | 小田義直, 類上皮細胞性腫瘍: 病理形態学キーワード , 病理と臨床 臨時増刊号 Vol. 28, 分光堂、354-355, 2010, 2010.04. |
| 377. | 小田義直, 書評：Dahlin’s Bone Tumors, 6th ed. LIPPINCOTT WILLIAMS & WILKINS , 病理と臨床 28(4): 457, 2010, 2010.04. |
| 378. | Yamamoto H, Miyamoto Y, Nishihara Y, Kojima A, Imamura M, Kishikawa K, Takase Y, Ario K, Oda Y, Tsuneyoshi M, Primary gastrointestinal stromal tumor of the liver with PDGFRA gene mutation: A case report with a review of literature. , Hum Pathol 41(4): 605-609, 2010, 2010.04. |
| 379. | 米増博俊、宋裕賢、甲斐友喜、渋谷忠正、今川全晴、小田義直, 腎粘液管状紡錘細胞癌(Mucinous tubular and spindle cell carcinoma)の一例 , 診断病理 27(3): 257-7260, 2010, 2010.03. |
| 380. | Endo M, Oda Y, Harimaya K, Tamiya S, Yamamaoto H, Kohashi K, Kurihara S, Setsu N, Matsuura S, Matono H, Matsuda S, Iwamoto Y, Tsuneysohi M:
, Low-grade dedifferentiated liposarcoma of the neck: magnetic resonance imaging and pathological correlation. , J Orthop Sci 15(1): 148-152, 2010 (Corresponding), 2010.01. |
| 381. | 小田義直, 整形外科専門医に必須な知識としての骨・軟部腫瘍の組織像 , 日本整形外科学会雑誌 84(1): 47-58, 2010, 2010.01. |
| 382. | 小田義直, 悪性線維性組織球腫（多形型、巨細胞型、炎症型）：整形外科医が知っておくべき骨・軟部腫瘍の組織像 , 整形外科 60(12): 1298-1299, 2009, 2009.12. |
| 383. | 孝橋賢一、小田義直、田口智章, 小児軟部腫瘍の病理診断と遺伝子異常 , 日本小児科学会雑誌 113(11): 1626-1635, 2009, 2009.11. |
| 384. | 小田義直, ヒト悪性腫瘍におけるYB-1およびCXCR4発現と悪性度の指標 特集：がん分子病理診断の新展開 , 医学のあゆみ 229 (10): 1008-1013, 2009, 2009.10. |
| 385. | 小田義直, 隆起性皮膚線維肉腫：整形外科医が知っておくべき骨・軟部腫瘍の組織像 , 整形外科 60(9): 1002-1003, 2009, 2009.09. |
| 386. | Kohashi K, Oda Y, Tsuneyoshi M, Direct evidence of mutational inactivation of SMARCB1/INI1 in epithelioid sarcoma-Reply. , Hum Pathol 40(9): 1362-1364, 2009, 2009.09. |
| 387. | 森松克哉、小田義直、孝橋賢一、西山憲一、横山良平、恒吉正澄, Proximal type epithelioid sarcomaの１例 , 診断病理 26(4): 257-259, 2009, 2009.08. |
| 388. | Koga Y, Matsuzaki A, Suminoe A, Hatano, M, Saito Y, Kinoshita Y, Tajiri T, Taguchi T, Kohashi K, Oda Y, Tsuneyoshi T, Hara T:
, Long-term survival after autologous peripheral blood stem cell transplantation in two patients with malignant rhabdoid tumor of the kidney. , Pediatr Blood Cancer 52(7): 888-890, 2009., 2009.07. |
| 389. | Oshiro Y, Kohashi K, Oda Y, Tsuneyoshi M, Shono Y
, Unclassified epithelioid vascular tumor with hemangioendotheliomatous feature and lymphatic differentiation: A case report. , Pathol Int 59(6): 410-414, 2009, 2009.06. |
| 390. | 本田由美、孝橋賢一、小田義直、恒吉正澄、猪山賢一, Angiomatoid fibrous histiocytomaの一例 , 診断病理 26(3): 151-154, 2009, 2009.06. |
| 391. | 小田義直, 粘液線維肉腫：整形外科医が知っておくべき骨・軟部腫瘍の組織像 , 整形外科 60(5): 466-467, 2009, 2009.05. |
| 392. | Nakamura T, Matsumine A, Kato H, Kusuzaki K, Nishimura K, Murata T, Shiraishi T, Oda Y, Tsuneyoshi M, Uchida A, Malignant melanoma with a rhabdoid phenotype exhibiting numerous solid tumor masses; A case report. , Oncol Rep 21(4): 887-891, 2009., 2009.04. |
| 393. | 小田義直, 顎関節領域に発生する腫瘤性病変の鑑別診断 /骨関節病変のエッセンスII ―非腫瘍性病変― , 病理と臨床 27(3): 218-224, 2009, 2009.03. |
| 394. | Oda Y, Tsuneyoshi M
, Recent advances of molecular pathology in soft tissue sarcoma: Their implications for diagnosis, patient’s prognosis, and molecular target therapy in the future , Cancer Sci 100(2): 200-208, 2009 (Corresponding), 2009.02. |
| 395. | 恒吉正澄、八尾隆史、小田義直、田宮貞史、相島慎一、山元英崇、大石善丈、平橋美奈子、栗原秀一、孝橋賢一
, ヒト悪性腫瘍の病理組織形態と分子生物学的特性 , 福岡医学雑誌 100(1): 12-25, 2009., 2009.01. |
| 396. | 小田義直, 軟部腫瘍の新たな概念:軟部腫瘍診断2009 , 臨床画像25(1): 6-15, 2009, 2009.01. |
| 397. | Kohashi K, Nakamori M, Oda Y, Yamamoto H, Tamiya S, Kurihara S, Tobo T, Kinoshita Y, Tajiri T, Taguchi T, Tsuneyoshi M:
, Multifocal metanephric adenoma in childhood: A case report. , Pathol Int 59(1): 49-52, 2009. (Corresponding), 2009.01. |
| 398. | 小田義直, 成人型線維肉腫:整形外科医が知っておくべき骨・軟部腫瘍の組織像 , 整形外科 59(12): 1464-1465, 2008., 2008.12. |
| 399. | Saito Y, Matsuzaki A, Suminoe A, Koga Y, Kurata H, Oda Y, Tsuneyoshi M, Hara T
, Congenital Ewing sarcoma in retroperitoneum with multiple metastases. , Pediatr Blood Cancer 51(5): 698-701, 2008, 2008.11. |
| 400. | Takayama Y, Yabuuchi H, Matsuo Y, Soeda H, Okafuji T, Kamitani T, Kinoshita Y, Kubokura N, Sakai S,
Oda Y, Hatakenaka M, Honda H:
, Computed tomographic and magnetic resonance features of inflammatory myofi broblastic tumor of the lung in children , Radiat Med 26(10): 613-617, 2008, 2008.10. |
| 401. | Takahara M, Ichikawa R, Oda Y, Uchi H, Takeuchi S, Moroi Y, Kiryu H, Furue M, Desmoplastic fibroblastoma; a case presenting as a protruding nodule in the dermis. , J Cutan Pathol Suppl. 1(10): 70-73, 2008, 2008.10. |
| 402. | Oda Y, Tsuneyoshi M
, Expression of multidrug resistance-related molecules and Y-box-binding protein-1 in soft-tissue sarcomas. , Nova Scientific Publisher (Corresponding), 2008.10. |
| 403. | 井久保丹、森藤良浩、新海健太郎、尾立西一、松成康生、中村和彦、松尾静香、古賀有希、松原不二夫、平方良輔、小田義直
, 十二指腸腫瘍による狭窄を契機に発見された同時性膵頭部および膵体部癌の１例 , 胆と膵 29(9): 873-878, 2008., 2008.09. |
| 404. | 小田義直
, 表在性線維腫症(Dupuytren型線維腫症)、デスモイド型線維腫症:整形外科医が知っておくべき骨・軟部腫瘍の組織像 , 整形外科 59(9): 1140-1141, 2008., 2008.09. |
| 405. | 小田義直
, 結節性筋膜炎:整形外科医が知っておくべき骨・軟部腫瘍の組織像 , 整形外科 59(3): 292-293, 2008., 2008.03. |
| 406. | 後藤綾子、小田義直、孝橋賢一、田尻達郎、田口智章、恒吉正澄：
, Clear cell sarcoma of the kidneyの1例 , 診断病理 25(3): 177-180, 2008., 2008.03. |
| 407. | Matsumoto Y, Matsuda S, Matono K, Oda Y, Tsuneyoshi M, Iwamoto Y
, Intra-articular osteochondroma of the knee joint in a patient with hereditary multiple osteochondromatosis. , Fukuoka Acta Med 98(12): 425-430, 2007., 2007.12. |
| 408. | Oda Y, Takahira T, Yokoyama R, Tsuneyoshi M, Diffuse-type giant cell tumor (GCT)/ pigmented villonodular synovitis (PVNS) arising in the sacrum: Malignant form. , Pathol Int 57(9): 627-631, 2007 (Corresponding), 2007.09. |
| 409. | Sakamoto A, Yoshida T, Matono H, Tanaka K, Matsuda S, Oda Y, Iwamoto Y, Dedifferentiated liposarcoma with leukocytosis. A case report. G-CSF-producing soft-tissue tumors, possible association with undifferentiated liposarcoma lineage. , World J Surg Oncol, 5(1): 131 (5 pages), 2007 (Online journal), 2007.08. |
| 410. | Ishimura M, Ohga S, Nagatoshi Y, Okamura J, Tajiri T, Kohashi K, Oda Y,
Takada H, Hara T
, Malignant hepatic tumor occurring 10 yrs after a histocompatible sibling donor bone marrow transplantation for severe aplastic anemia. , Pediatr Transplant 11(8):945-949, 2007, 2007.08. |
| 411. | 小田義直、恒吉正澄
, 軟部肉腫の遺伝子診断と分子生物学的予後因子 , 福岡医学会雑誌98(7): 287-294, 2007, 2007.07. |
| 412. | Sakamoto A, Yoshida T, Matsuura S, Tanaka K, Matsuda S, Oda Y, Hori Y, Yokomizo A, Iwamoto Y, Metastasis to the gluteus muscle from renal cell carcinoma with special emphasis on MRI features , World J Surg Oncol 5: 88 (4pages), 2007 (Online journal), 2007.06. |
| 413. | Yoshida T, Sakamoto A, Tanaka K, Matsuda S, Oda Y, IwamotoY
, Alternative surgical treatment for giant-cell reparative granuloma in the metacarpal bone of the hand, ulilizing phenol and ethanol adjuvant therapy. , J Hand Surg (Am) 32 (6): 887-892, 2007 , 2007.06. |
| 414. | Sakamoto A, Yamamoto H, Yoshida T, Tanaka K, Matsuda S, Oda Y, Tsuneyoshi M, Iwamoto Y, Desmoplastic fibroblastoma (collagenous fibroma) with a specific breakpoint of 11q12., Histopathology 51(6), 859-860, 2007, 2007.06. |
| 415. | Kinoshita Y, Tajiri T, Ieiri S, Nagata K, Taguchi T, Suita S, Yamazaki K, Yoshino I, Maehara Y, Kohashi K, Yamamoto H, Oda Y, Tsuneyoshi M, A case of an inflammatory myofibroblastic tumor in the lung which expressed TPM3-ALK gene fusion., Pediatr Surg Int 23(6): 595-599, 2007, 2007.06. |
| 416. | 仲田興平、山元英崇、今村公一、中川真宗、井上崇弘、小田義直、恒吉正澄
, 軟骨化生を伴う乳癌の１例 , 診断病理24: 220-223, 2007, 2007.05. |
| 417. | 小田義直、恒吉正澄, 炎症性偽腫瘍と鑑別すべき炎症性腫瘍および腫瘍状病変 , 病理と臨床25: 459-465, 2007, 2007.05. |
| 418. | Miyajima K, Hasegawa S, Oda Y, Toyoshima S, Tsuneyoshi M, Motooka M,
Matsuura Y, Ishioka H, Ono M:
, Angiomyofibroblastoma-like tumor (cellular angiofibroma) in the male inguinal region. , Radiat Med 25(4): 173-177, 2007, 2007.04. |
| 419. | Sakamoto A, Yoshida T, Yamamoto H, Oda Y, Tsuneyoshi M, Iwamoto Y
, Congenital pseudoarthrosis of the tibia. An analysis of the histology and NF1 gene: Case study. , J Orthop Sci 12(4): 361-365, 2007, 2007.04. |
| 420. | 山口敢、古賀友紀、住江愛子、斎藤祐介、松崎彰信、神野俊介、瀧本智仁、
須田正洋、小田義直、武藤敏孝、高月浩、原寿郎:
, 初発時に急性白血病様の骨髄像を呈した原発不明胞巣型横紋筋肉腫 , 臨床血液48(4): 315-320, 2007, 2007.04. |
| 421. | Yoshida T, Sakamoto A, Tanaka K, Iwamoto Y, Oda Y, Izumi T, Tsuneyoshi M, Intramuscular diffuse-type giant cell tumor within hamstring muscle., Skeletal Radiol 36; 331-333, 2007., 2007.03. |
| 422. | 小田義直, グロムス腫瘍：整形外科医が知っておくべき骨・軟部腫瘍の組織像, 整形外科 58: 438-439, 2007., 2007.01. |
| 423. | 小田義直, 腱鞘巨細胞腫、色素性絨毛結節性滑膜炎：整形外科医が知っておくべき骨・軟部腫瘍の組織像, 整形外科 58: 298-299, 2007., 2007.01. |
| 424. | 小田義直, 滑膜肉腫：整形外科医が知っておくべき骨・軟部腫瘍の組織像, 整形外科 58: 198-199, 2007., 2007.01. |
| 425. | 米増博俊、今村公一、小田義直、犬塚貞明、福澤謙吾、若杉健三、恒吉正澄, 横行結腸間膜に発生した胃腸管外間質腫瘍 extragastrointestinal stromal tumor (EGIST) の一例, 診断病理 24: 86-88, 2007., 2007.01. |
| 426. | Sakamoto A, Tanaka K, Matsuda S, Oda Y, Tsuneyoshi M, Iwamoto Y, Aneurysmal bone cyst of the capitate: a case report and a review emphasizing local recurrence., Fukuoka Acta Med 97:302-7, 2006., 2006.01. |
| 427. | Sakamoto A, Tanaka K, Matsuda S, Harimaya K, Nakamura T, Oda Y, Tsuneyoshi M, Iwamoto Y, Adventitial cystic disease of the popliteal vein: report of a case., Surg Today 12: 1098-100, 2006., 2006.01. |
| 428. | Sakamoto A, Yoshida T, Matsuda S, Tanaka K, Kobayashi C, Oda Y, Tsuneyoshi M, Iwamoto Y, Chondromyxoid fibroma of the clavicle., J Orthop Sci 11; 533-536, 2006., 2006.01. |
| 429. | Sakamoto A, Yamamoto H, Tanaka K, Matsuda S, Harimaya K, Oda Y, Tsuneyoshi M, Iwamoto Y, Dedifferentiated chondrosarcoma with leukocytosis and elevation of serum G-CSF. A case report., World J Surg Oncol 4; 37 (7 pages): 2006. (Online journal), 2006.01. |
| 430. | Matsuo Y, Sakai S, Yabuuchi H, Soeda H, Takahashi N, Okafuji T, Yoshimitsu K, Koga H, Yoshino I, Oda Y, Nakamura Y, Honda H., A case of pulmonary synovial sarcoma diagnosed with detection of chimera gene. Imaging findings., Clin Imaging 30: 60-2, 2006, 2006.01. |
| 431. | Yamamoto H, Oda Y, Yao T, Oiwa T, Kobayashi C, Tamiya S, Kawaguchi K, Hino O, Tsuneyoshi M, Malignant perivascular epithelioid cell tumor of the colon: Report of a case with molecular analysis., Pathol Int 56: 46-50, 2006, 2006.01. |
| 432. | 小田義直、恒吉正澄, 粘液-円形細胞型脂肪肉腫における分子生物学的悪性度評価, 細胞 38: 390-393, 2006., 2006.01. |
| 433. | Oda Y, Tsuneyoshi M, Letter to the editor; Re: Oda et al. Frequent alteration of p16INK4a/p14ARF and p53 pathways in the round cell component of myxoid/round cell liposarcoma: p53gene alterations and reduced p14ARF expression both correlate with poor prognosis. Author's reply, J Pathol 209: 282, 2006., 2006.01. |
| 434. | 孝橋賢一、小田義直、木下義晶、田尻達郎、高橋由紀子、田口智章、水田祥代、恒吉正澄, hSNF5/INI1遺伝子の全欠失を認めた腎悪性ラブドイド腫瘍の１例, 診断病理 23: 132-135, 2006., 2006.01. |
| 435. | Ohishi Y, Kaneki E, Tamiya S, Oda Y, Hirakawa T, Miyamoto S, Kaku T, Nakano H, Tsuneyoshi M, Role of immunohistochemical expression of Ki-67 in ovarian carcinoma., Handbook of Immunohistochemistry and in situ Hybridization of Human Carcinomas, Hayat MA (Edt), Volume 4: Molecular Genetics,Gastrointestinal Carcinoma, and Ovarian Carcinoma, Elsevier Academic Press, London, 2006, pp363-370., 2006.01. |
| 436. | Shimonodan H, Nagayama J, Nagatoshi Y, Hatanaka M, Takada A, Iguchi H, Oda Y, Okamura J, Acute lymphocytic leukemia in adolescence with multiple osteolytic lesion and hypercalcemia mediated by lymphoblast-producing parathyroid hormone-related peptide: A case report and review of the literature., Pediatric Blood and Cancer 45: 333-339, 2005, 2005.01. |
| 437. | Saito T, Oda Y , Kawaguchi K, Tanaka K, Matsuda S, Sakamoto A, Iwamoto Y, Tsuneyoshi M, Five-year evoluation of a telangiectatic osteosarcoma initially managed as an aneurysmal bone cyst., Skeletal Radiol 34: 290-294, 2005., 2005.01. |
| 438. | 孝橋賢一、小田義直、高比良知也、蜂須賀淳一、恒吉正澄, COL1A1-PDGFB融合遺伝子が検出された線維肉腫の成分を含む隆起性皮膚線維肉腫の１例, 診断病理 22: 239-241, 2005., 2005.01. |
| 439. | 高比良知也、小田義直、恒吉正澄, 線維性線維組織球性腫瘍の診断をめぐる問題点とその診断, 臨床画像 21: 438-444, 2005., 2005.01. |
| 440. | 岩佐厚子、兼城英輔、小田義直、小川伸二、尼田覚、平川俊夫、恒吉正澄, Female adnexal tumor of probable wolffian origin (FATWO)の１例, 診断病理 22: 171-174, 2005., 2005.01. |
| 441. | Kiyoshima K, Oda Y, Nakamura T, Migita T, Okumura K, Naito S, Tsuneyoshi M:, Multicentric papillary renal cell carcinoma associated with renal adenomatosis., Pathol Int 54: 266-272, 2004., 2004.06. |
| 442. | Niwa H, Masuda S, Kobayashi C, Oda Y, Pulmonary synovial sarcoma with polypoid endobronchial growth: A case report, immunohistochemical and cytogenetic study., Pathol Int 54: 611-615, 2004., 2004.01. |
| 443. | 小田義直, 骨軟部腫瘍野WHO分類2002年改訂；軟部腫瘍の変更点について整形外科の先生方へ, 骨・関節・靭帯 17: 1141-1149, 2004, 2004.01. |
| 444. | 泉貞有、小田義直、松田秀一、田仲和宏、岩本幸英、恒吉正澄, 脛腓骨同時発生のosteofibrous dysplasiaの一例, 診断病理 21: 251-253, 2004., 2004.01. |
| 445. | 川口謙一、小田義直、恒吉正澄, 骨腫瘍類似疾患の鑑別診断と問題点；骨軟部腫瘍：新WHO分類をふまえてII-骨腫瘍, 病理と臨床 22: 270-276, 2004., 2004.01. |
| 446. | 兼城英輔、大石善丈、田宮貞史、河野善明、平川俊夫、小田義直、恒吉正澄, 子宮内膜間質平滑筋混合腫瘍の1例, 診断病理 21: 80-83, 2004., 2004.01. |
| 447. | 小田義直、恒吉正澄, 筋原性腫瘍について； 骨軟部腫瘍：新WHO分類をふまえてI-軟部腫瘍, 病理と臨床 22: 146-159, 2004., 2004.01. |
| 448. | Harimaya K, Oda Y, Matsuda S, Tanaka K, Sakamoto A, Chuman K, Iwamoto Y:, Primitive neuroectodermal tumor and extraskeletal Ewing's sarcoma arising primarily around the spinal colum: report of four cases and review of the literature., Spine 28: E408-412, 2003., 2003.01. |
| 449. | Yamaguchi M, Yoshino I, Osoegawa A, Kameyama T, Tagawa T, Fukuyama S, A, Kameyama T, Tagawa T, Fukuyama S,, Inflammatory myofibroblastic tumor of the mediastinum presenting as superior vena cava syndrome., J Thorac Cardiovasc Surg 26; 870-872, 2003., 2003.01. |
| 450. | Yamamoto H, Shiratsuchi H, Yao T, Uryu H, Oda Y, Tamiya S, Tsuneyoshi M:, ALK-positive anaplastic large cell lymphoma of the parotid gland., Histopathology 43: 397-398, 2003., 2003.01. |
| 451. | Saito T, Oda Y, Tanaka K, Matsuda S, Sakamoto A, Yamamoto H , Iwamoto Y, Tsuneyoshi M:, Low-grade fibrosarcoma of the proximal humerus. A case report with a review of literatures., Pathol Int 53: 115-120, 2003., 2003.01. |
| 452. | Kikuchi I, Anbo J, Nakamura S, Sugai T, Sasou S, Yamamoto M, Oda Y, Shiratsuchi H, Tsuneyoshi M:, Synovial sarcoma of the thyroid: Report of a case with aspiration cytology findings and gene analysis., Acta Cytologica 47: 495-500, 2003., 2003.01. |
| 453. | Adachi T, Oda Y, Sakamoto A, Saito T, Tamiya S, Hachitanda Y, Masuda S, Tsuneyoshi M, Mixed tumor of deep soft tissue, Pathol Int 53: 35-39, 2003., 2003.01. |
| 454. | 小田義直, 巨細胞性線維芽細胞腫の病態, 日本医事新報 第4146号: 98-99, 2003, 2003.01. |
| 455. | 山元英崇、恵良昭一、小田義直、恒吉正澄:, 下腿のPleomorphic hyalinizing angiectatic tumorの１例, 診断病理 20(3): 299-300, 2003, 2003.01. |
| 456. | Ehara S, Oda Y:, Letter to the Editor; Infantile fibromatosis., Am J Roentgenol 180; 284, 2003., 2003.01. |
| 457. | 高橋由紀子、小田義直、八反田洋一、恒吉正澄, 横紋筋肉腫の病理診断からみた予後, 小児外科 35: 25-30, 2003., 2003.01. |
| 458. | Kawaguchi K, Oda Y, Nakanishi K, Saito T, Tamiya S, Nakahara K, Matsuoka H, Tsuneyoshi M, Malignant transformation of renal angiomyolipoma: A case report., Am J Surg Pathol 26: 523-529, 2002., 2002.01. |
| 459. | 八尾隆史、大屋正文、西山憲一、田口健一、中村俊彦、小田義直、恒吉正澄:, 病理学的に胃癌と鑑別する必要がある炎症性病変, 胃と腸 37: 1715-1723, 2002., 2002.01. |
| 460. | Ehara S, Oda Y, Letter to the Editor; Deep dermatofibrosarcoma protuberans., Am J Roentgenol 179; 1643, 2002. , 2002.01. |
| 461. | 大庭功一、武井明、名取省、新井堅、中西和夫、小田義直: , 左腹壁の骨化性筋炎の像を呈したphosphaturic mesenchymal tumorによる腫瘍性骨軟化症の一例, 日本内科学会雑誌 創立100周年記念号 第91巻 230-232, 2002. , 2002.01. |
| 462. | 小田義直、恒吉正澄, 軟部肉腫の遺伝子診断と多剤耐性遺伝子発現, 大阪医薬品協会 会報 平成14年11月・第646号 pp1-9, 2002.01. |
| 463. | 小田義直、恒吉正澄, 骨肉腫と良性病変との鑑別, 病理と臨床 20: 795-811, 2002, 2002.01. |
| 464. | 小田義直:, 悪性軟部ラブドイド腫瘍 Malignant rhabdoid tumor of soft parts, 病理と臨床 20: 526-527, 2002, 2002.01. |
| 465. | 高橋由紀子、小田義直、恒吉正澄:, 悪性線維性組織球腫の最新知見-悪性線維性組織球腫と類血管腫線維性組織球腫:特に小児発生例について-, 小児外科 34: 463-468, 2002, 2002.01. |
| 466. | Oda Y, Tsuneyoshi M, Letter to the Editor; Leiomyosarcoma versus myofibrosarcoma. Author's reply, Am J Surg Pathol 26; 394-396, 2002, 2002.01. |
| 467. | 小田義直、高橋由紀子、恒吉正澄:, 小児の線維腫症とその鑑別を要する疾患., 小児外科 34: 165-175, 2002, 2002.01. |
| 468. | Sakamoto A, Oda Y, Nagayoshi Y, Iwakiri K, Tamiya S, Iwamoto Y, Tsuneyoshi M, Glomangiopericytoma causing oncologic osteomalacia. A case report with immunohistochemical analysis., Arch Orthop Trauma Surg 121: 104-108, 2001, 2001.01. |
| 469. | 坂本昭夫、小田義直、恒吉正澄, 軟部腫瘍診断のpitfall., Monthly Book Orthopaedics 14: 63-76, 2001, 2001.01. |
| 470. | 斎藤剛、小田義直、恒吉正澄, 滑膜肉腫における細胞間接着分子の発現とβ-cateninの核内発現:その臨床病理学的意義, 現代医療 33: 253-257, 2001, 2001.01. |
| 471. | Oda Y, Kinoshita Y, Tamiya S, Iwamoto Y, Tsuneyoshi M:, Extraskeletal primitive neuroectodermal tumor with massive osteo-cartilaginous metaplasia., Histopathology 36: 188-191, 2000, 2000.01. |
| 472. | Kitamura T, Oda Y, Matsuda S, Kubota H, Iwamoto Y:, Nerve sheath ganglion of the ulnar nerve., Arch Orthop Trauma Surg 120: 108-109, 2000, 2000.01. |
| 473. | 小田義直、恒吉正澄, 泌尿生殖器系臓器の肉腫, 病理と臨床 18: 908-918, 2000, 2000.01. |
| 474. | 渡辺哲雄、小田義直、恒吉正澄, 軟部腫瘍の病理, 臨床画像 16: 385-394, 2000, 2000.01. |
| 475. | 小田義直、恒吉正澄, 巨細胞性線維芽細胞腫および隆起性皮膚線維肉腫, 病理と臨床 18: 123-128, 2000, 2000.01. |
| 476. | Saito T, Terada K, Tsuchiya K, Oda Y, Tsuneyoshi M, Iwamoto Y, Lymphangioma presenting as a dumbell tumor in the epidural space of the lumbar spine., Spine 24: 74-76, 1999, 1999.01. |
| 477. | 小田義直、恒吉正澄, 低悪性線維粘液肉腫, 病理と臨床 17: 937-938, 1999, 1999.01. |
| 478. | 小田義直、恒吉正澄, 小児の軟部組織の線維腫症、その他の類似病変, 病理と臨床 17: 456-462, 1999, 1999.01. |
| 479. | 斎藤太一、松田秀一、小田義直、 寺田和正、土屋邦喜、岩本幸英, 仙骨脊索腫に対する手術症例の検討, 西日本脊椎研究会誌 24: 187-190, 1998, 1998.01. |
| 480. | Kawaguchi K, Oda Y, Miura H, Watanabe T, Tsuneyoshi M, Iwamoto Y:, Periostel osteoblastoma of the distal humerus. A case report., J Orthop Science 3: 341-345, 1998, 1998.01. |
| 481. | 小田義直、岩本幸英, 骨肉腫における転写因子YB-1蛋白の発現, 骨・関節・靭帯 11: 1499-1501, 1998, 1998.01. |
| 482. | 小田義直, Vocabulary; MRP, 整形外科 49: 705, 1998, 1998.01. |
| 483. | 松田秀一、小田義直、播磨谷勝三、岩本幸英, 切除不能な仙骨、骨盤部発生の原発性悪性腫瘍に対する治療, 西日本脊椎研究会誌 24: 218-221, 1998., 1998.01. |
| 484. | 小田義直、岩本幸英, 左前腕の腫瘤にて来院した21歳女性（胞巣状軟部肉腫）. pp95-99, 整形外科専門医を目指すケース・メソッド・アプローチ ５ 骨軟部腫瘍. 日本医事新報社、東京, 1998.01. |
| 485. | 小田義直、岩本幸英, von Recklinghausen病に左下腿部以下の疼痛、しびれ、膝の腫瘤が出現した27歳男性（von Recklinghausen病に伴う悪性神経鞘腫）. pp80-85, 整形外科専門医を目指すケース・メソッド・アプローチ ５ 骨軟部腫瘍. 日本医事新報社、東京, 1998.01. |
| 486. | 小田義直、岩本幸英, 左大腿外側の腫瘤を認めた62歳男性（軟部悪性線維性組織球腫）. pp74-79, 整形外科専門医を目指すケース・メソッド・アプローチ ５ 骨軟部腫瘍. 日本医事新報社、東京, 1998.01. |
| 487. | 小田義直、岩本幸英, 増強する左膝痛、膝か部腫瘤を訴えて来院した33歳男性（滑膜肉腫）. pp67-73, 整形外科専門医を目指すケース・メソッド・アプローチ ５ 骨軟部腫瘍. 日本医事新報社、東京, 1998.01. |
| 488. | 小田義直、岩本幸英, 左大腿近位部の疼痛とX線上異常陰影を指摘され来院した 50歳男性（転移性骨腫瘍）. pp55-60, 整形外科専門医を目指すケース・メソッド・アプローチ ５ 骨軟部腫瘍. 日本医事新報社、東京, 1998.01. |
| 489. | 小田義直、岩本幸英, 右膝内側の疼痛、跛行を認める23歳女性（骨巨細胞腫）. pp49-54, 整形外科専門医を目指すケース・メソッド・アプローチ ５ 骨軟部腫瘍. 日本医事新報社、東京, 1998.01. |
| 490. | 小田義直、岩本幸英, 左上腕痛、左肩の疼痛をきたした75歳男性（軟骨肉腫）. pp36-42, 整形外科専門医を目指すケース・メソッド・アプローチ ５ 骨軟部腫瘍. 日本医事新報社、東京, 1998.01. |
| 491. | Y Okumura, M Komoda, S Tamura, H Kumagai, T Shirakawa, Shuji Arita, Ariyama Hiroshi, hitoshi kusaba, UMENO JUNJI, Matsumoto Takuya, Hidetaka Yamamoto, Yoshinao Oda, koichi akashi, Eishi Baba, Anti-HER2 combinationchemotherapy for advanced gastric cancer associated with the Peutz-Jeghers syndrome: a case report and literature review., Int Cancer Conf J, in press . |
| 492. | Kenzo Sonoda, M Nogami, M Naka, F Ookubo, H Kobayashi, Hideaki Yahata, Okugawa Kaoru, Kaneki Eisuke, Yoshinao Oda, Kiyoko Kato, Charactetristic cytological features of cervical clear cell adenocarcinoma: A report of 4 cases., J Cytol Histol 4:5, 2013. |
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