病態病理学分野│群馬大学大学院 医学系研究科 高次機能統御系脳神経病理生体制御学

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業績集

業績集

Results

2018年度

  1. 横尾英明、中里洋一(分担執筆). カラーアトラス病理組織の見方と鑑別診断(第6版), 医歯薬出版, 2018.

  2. 山田勢至、横尾英明. 臨床医のための神経病理再入門. 上衣. Clinical Neuroscience. 36(4): 398-399, 2018.

  3. 山﨑文子, 横尾英明. 臨床医のための神経病理再入門. 膠芽腫. Clinical Neuroscience, 36(12): 1390-1392, 2018.

  4. 竹渕友弥、佐野孝昭、 後藤優典、星川里美、栗原康哲、伊古田勇人、平戸純子、小山徹也. 甲状腺に病変を形成したランゲルハンス細胞組織球症の1例. 日本臨床細胞学会雑誌, 57(3): 177-182, 2018.

  5. Shin SA, Ahn B, Kim SK, Kang HJ, Nobusawa S, Komori T, Park SH. Brainstem astroblastoma with MN1 translocation. Neuropathology, 38(6): 631-637, 2018.

  6. Yoshida Y, Nobusawa S, Nakata S, Nakada M, Arakawa Y, Mineharu Y, Sugita Y, Yoshioka T, Araki A, Sato Y, Takeshima H, Okada M, Nishi A, Yamazaki T, Kohashi K, Oda Y, Hirato J, Yokoo H. CNS high-grade neuroepithelial tumor with BCOR internal tandem duplication: a comparison with its counterparts in the kidney and soft tissue. Brain Pathol, 28(5): 710-720, 2018.

  7. Hirose T, Nobusawa S, Sugiyama K, Amatya VJ, Fujimoto N, Sasaki A, Mikami Y, Tanaka S, Yokoo H. Astroblastoma: A distinct tumor entity characterized by alterations of the X chromosome and MN1 rearrangement. Brain Pathol, 28(5): 684-694, 2018.

  8. Nakajima N, Nobusawa S, Nakata S, Nakada M, Yamazaki T, Matsumura N, Harada K, Matsuda H, Funata N, Nagai S, Nakamura H, Sasaki A, Akimoto J, Hirato J, Yokoo H. BRAF V600E, TERT promoter mutations and CDKN2A/B homozygous deletions are frequent in epithelioid glioblastomas: A histological and molecular analysis focusing on intratumoral heterogeneity. Brain Pathol, 28(5): 663-673, 2018.

  9. Okonogi N, Suzuki Y, Sato H, Oike T, Yoshimoto Y, Mimura K, Noda S, Okamoto M, Tamaki T, Ohgaki H, Yokoo H, Nakano T. Combination therapy of intravenously injected microglia and radiotherapy prolongs survival in a rat model of spontaneous malignant glioma. Int J Radiat Oncol Biol Phys, 102(3): 601-608, 2018.

  10. Murakami C, Yamazaki T, Shintoku R, Aihara M, Yoshimoto Y, Matsumura N, Nobusawa S, Ikota H, Hirato J, Yokoo H. Anaplastic ganglioglioma with epithelioid cell components. Neuropathology, 38(5): 498-502, 2018.

  11. Yajima T, Mogi A, Shimizu K, Kosaka T, Nagashima T, Ohtaki Y, Obayashi K, Nakazawa S, Iijima M, Yoshida Y, Hirato J, Kuwano H. Ectopic thymoma in the paratracheal region of the middle mediastinum: a rare case report and literature review. BMC Res Notes, 11(1):256, 2018.

  12. Kubo N, Harimoto N, Araki K, Hagiwara K, Yamanaka T, Ishii N, Tsukagoshi M, Igarashi T, Watanabe A, Miyazaki M, Yokoo H, Kuwano H, Shirabe K. The Feature of Solitary Small Nodular Type of Hepatic Epithelioid Hemangioendothelioma. Case Rep Gastroenterol, 12(2): 402-410, 2018.

  13. Murata K, Koga Y, Kasahara N, Hachisu Y, Nunomura S, Nakajima N, Yokoo H, Kaira K, Maeno T, Dobashi K, Izuhara K, Hisada T. Accumulation of periostin in acute exacerbation of familial idiopathic pulmonary fibrosis. J Thorac Dis, 10(7): E587-E591, 2018.

  14. Matsumura N, Ikota H, Yamazaki T, Nakata S, Nobusawa S, Hirato J, Yoshimoto Y, Yokoo H. Cerebellar high-grade astrocytoma with IDH mutations in the elderly: a report of two cases. Neuropathology, 38(4): 411-416, 2018.

  15. Yoshida Y, Ide M, Fujimaki H, Matsumura N, Nobusawa S, Ikota H, Yokoo H. Gliosarcoma with primitive neuronal, chondroid, osteoid, and ependymal elements. Neuropathology, 38(4): 392-399, 2018.

  16. Yamada SM, Tomita Y, Shibui S, Takahashi M, Kawamoto M, Nobusawa S, Hirato J. Primary spinal cord astroblastoma: case report. J Neurosurg Spine, 28(6): 642-646, 2018.

  17. Tomomasa R, Nakata S, Nobusawa S, Horiguchi K, Matsumura N, Ikota H, Hirato J, Yoshimoto Y, Yokoo H. Primary diffuse leptomeningeal atypical teratoid/rhabdoid tumor diagnosed by cerebrospinal fluid cytology: Case report with molecular genetic analysis. Hum Pathol, 77: 116-120, 2018.

  18. Harimoto N, Hagiwara K, Yamanaka T, Ishii N, Igarashi T, Watanabe A, Kubo N, Araki K, Ikota H, Suyama M, Maki T, Aishima S, Kuwano H, Shirabe K. Fairly rare clear cell adenocarcinoma mimicking liver cancer: a case report. Surg Case Rep, 4(1): 97, 2018.

  19. Hagiwara K, Araki K, Yamanaka T, Ishii N, Igarashi T, Watanabe A, Kubo N, Harimoto N, Kuwano H, Nobusawa S, Aishima S, Shirabe K. Resected primary mucinous cholangiocarcinoma of the liver. Surg Case Rep, 4(1): 41, 2018.

  20. Kumakura Y, Yokobori T, Yoshida T, Hara K, Sakai M, Sohda M, Miyazaki T, Yokoo H, Handa T, Oyama T, Yorifuji H, Kuwano H. Elucidation of the Anatomical Mechanism of Nodal Skip Metastasis in Superficial Thoracic Esophageal Squamous Cell Carcinoma. Ann Surg Oncol, 25(5): 1221-1228, 2018.

  21. Arai H, Nobusawa S, Kawabata-Iwakawa R, Rokudai S, Higuchi T, Yamazaki T, Horiguchi J, Sano T, Kojima M, Nishiyama M, Yokoo H, Hirato J, Oyama T. Myeloid sarcoma arising in malignant phyllodes tumour: clonal relationships revealed by comparative genome-wide analyses. Br J Haematol, 181(2): 255-259, 2018.

  22. Johann PD, Bens S, Oyen F, Wagener R, Giannini C, Perry A, Raisanen JM, Reis GF, Nobusawa S, Arita K, Felsberg J, Reifenberger G, Agaimy A, Buslei R, Capper D, Pfister SM, Schneppenheim R, Siebert R, Fruhwald MC, Paulus W, Kool M, Hasselblatt M. Sellar Region Atypical Teratoid/Rhabdoid Tumors (ATRT) in Adults Display DNA Methylation Profiles of the ATRT-MYC Subgroup. Am J Surg Pathol, 42(4): 506-511, 2018.

  23. Vaubel RA, Caron AA, Yamada S, Decker PA, Eckel Passow JE, Rodriguez FJ, Nageswara Rao AA, Lachance D, Parney I, Jenkins R, Giannini C. Recurrent copy number alterations in low-grade and anaplastic pleomorphic xanthoastrocytoma with and without BRAF V600E mutation. Brain Pathol, 28(2): 172-182, 2018.

  24. Okada J, Matsumoto S, Kaira K, Saito T, Yamada E, Yokoo H, Katoh R, Kusano M, Okada S, Yamada M. Sodium glucose cotransporter 2 inhibition combined with cetuximab significantly reduced tumor size and carcinoembryonic antigen level in colon cancer metastatic to liver. Clin Colorectal Cancer, 17(1): e45-e48, 2018.

  25. Funata N, Nobusawa S, Nakata S, Yamazaki T, Takabagake K, Koike T, Maegawa T, Yamada R, Shinoura N, Mine Y. A case report of adult cerebellar high-grade glioma with H3.1 K27M mutation: a rare example of an H3 K27M mutant cerebellar tumor. Brain Tumor Pathol, 35(1): 29-35, 2018.

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