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雑誌文献

Neurological Surgery 脳神経外科51巻5号

2023年09月発行

文献概要

特集 臨床脳神経外科医にとってのWHO脳腫瘍分類第5版 Ⅰ WHO脳腫瘍分類第5版の概要

トルコ鞍部腫瘍の分類・診断

著者: 西岡宏1

所属機関: 1虎の門病院間脳下垂体外科

ページ範囲:P.789 - P.798

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・臨床病理学的見地から,下垂体腺腫は下垂体神経内分泌腫瘍(PitNET)へ名称が変更された.
・PitNETの組織分類の基本は,下垂体転写因子(PIT1, TPIT, SF1)の免疫組織化学になった.
・腫瘍増殖能の指標(Ki67指数)の有用性や,特定の組織型の腫瘍がaggressiveな臨床経過を呈しやすいことは示されたが,PitNETのgrade分類は提示されなかった.
・エナメル上皮腫型と乳頭型の頭蓋咽頭腫は,おのおのCTNNB1変異とBRAF変異を呈する独立した個別の組織型になった.
・下垂体細胞腫,顆粒細胞腫などTTF1陽性の4型の後葉(神経下垂体)腫瘍は,下垂体細胞(pituicyte)由来腫瘍として統一された.

参考文献

1)Asa SL, et al;attendees of 14th Meeting of the International Pituitary Pathology Club, Annecy, France, November 2016:From pituitary adenoma to pituitary neuroendocrine tumor(PitNET):an International Pituitary Pathology Club proposal. Endocr Relat Cancer 24:C5-C8, 2017 doi:10.1530/ERC-17-0004
2)Asa SL, et al:Pituitary neuroendocrine tumors(PitNETs):nomenclature evolution, not clinical revolution. Pituitary 23:322-325, 2020
3)Ho K, et al:Pituitary neoplasm nomenclature workshop:does adenoma stand the test of time? J Endocr Soc 5:bvaa205, 2021 doi:10.1210/jendso/bvaa205
4)Rindi G, Inzani F:Neuroendocrine neoplasm update:toward universal nomenclature. Endocr Relat Cancer 27:R211-R218, 2020 doi:10.1530/ERC-20-0036
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6)Nishioka H, et al:The complementary role of transcription factors in the accurate diagnosis of clinically nonfunctioning pituitary adenomas. Endocr Pathol 26:349-355, 2015
7)Inoshita N, et al:Immunohistochemical and ultrastructural review of six cases previously diagnosed as null cell PitNETs. Brain Tumor Pathol 40:158-162, 2023
8)Asa SL, et al:Overview of the 2022 WHO classification of pituitary tumors. Endocr Pathol 33:6-26, 2022
9)Lopes MBS, et al:Pituitary adenoma/pituitary neuroendocrine tumour. WHO Classification of Tumours. Central Nervous System Tumours(5th edition). IARC, Lyon, 2021, pp. 406-414
10)Mete O, Asa SL:Structure, function, and morphology in the classification of pituitary neuroendocrine tumors:the importance of routine analysis of pituitary transcription factors. Endocr Pathol 31:330-336, 2020
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12)Trouillas J, et al:A new prognostic clinicopathological classification of pituitary adenomas:a multicentric case-control study of 410 patients with 8 years post-operative follow-up. Acta Neuropathol 126:123-135, 2013
13)Dai C, et al:Refractory pituitary adenoma:a novel classification for pituitary tumors. Oncotarget 7:83657-83668, 2016
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15)Trouillas J, et al:Aggressive pituitary tumours and carcinomas:two sides of the same coin? Eur J Endocrinol 178:C7-C9, 2018 doi:10.1530/EJE-18-0250
16)Goschzik T, et al:Genomic alterations of adamantinomatous and papillary craniopharyngioma. J Neuropathol Exp Neurol 76:126-134, 2017
17)Fukuhara N, et al:Immunohistochemistry or molecular analysis:which method is better for subtyping craniopharyngioma? Endocr Pathol 32:262-268, 2021
18)Santagata S, et al:Adamantinomatous craniopharyngioma. WHO Classification of Tumours. Central Nervous System tumours(5th edition). IARC, Lyon, 2021, pp. 393-396
19)Santagata S, et al:Papillary craniopharyngioma. WHO Classification of Tumours. Central Nervous System tumours(5th edition). IARC, Lyon, 2021, pp. 397-400
mutations. Acta Neuropathol 128:111-122, 2014
21)Lopes MBS, et al:Pituicytoma, granular cell tumor of the sellar region, and spindle cell oncocytoma. WHO Classification of Tumours. Central Nervous System Tumours(5th edition). IARC, Lyon, 2021, pp. 401-405
22)Asa SL, et al:Hypothalamic vasopressin-producing tumors:often inappropriate diuresis but occasionally Cushing disease. Am J Surg Pathol 43:251-260, 2019

掲載誌情報

出版社:株式会社医学書院

電子版ISSN:1882-1251

印刷版ISSN:0301-2603

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