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上皮样胶质母细胞瘤和伴发的低级别星形细胞瘤中TERT启动子与BRAF V600E的同时突变

Concurrent TERT promoter and BRAF V600E mutation in epithelioid glioblastoma and concomitant low-grade astrocytoma.

作者信息

Matsumura Nozomi, Nakajima Nozomi, Yamazaki Tatsuya, Nagano Takuro, Kagoshima Kaie, Nobusawa Sumihito, Ikota Hayato, Yokoo Hideaki

机构信息

Department of Human Pathology, Gunma University Graduate School of Medicine, Maebashi, Japan.

Department of Neurosurgery, Ohta Memorial Hospital, Ohta, Japan.

出版信息

Neuropathology. 2017 Feb;37(1):58-63. doi: 10.1111/neup.12318. Epub 2016 Jun 15.

Abstract

Epithelioid glioblastoma (E-GBM) is a rare variant of glioblastoma (GBM), characterized by epithelioid cells with eosinophilic round cytoplasm devoid of stellate cytoplasmic processes. A number of studies have demonstrated that more than half of E-GBMs harbor a valine to glutamic acid substitution at position 600 of the serine/threonine-protein kinase BRAF (BRAF V600E). However, there are no previous reports on E-GBM with telomerase reverse transcriptase (TERT) promoter mutation in addition to BRAF V600E mutation. Here, we report an E-GBM case in an 18-year-old man with BRAF V600E and TERT promoter mutations. The tumor composed of 80% E-GBM and 20% diffuse astrocytoma-like components, and BRAF V600E and TERT promoter mutations were detected in both. E-GBM generally arises as a primary lesion; however, a few previous cases have been demonstrated to accompany low-grade areas. Demonstration of concurrent BRAF V600E and TERT promoter mutations in low- and high-grade lesions strongly suggested their identical origin, and acquisition of each mutation may be an early event, possibly playing a pivotal role in the genesis and subsequent progression to E-GBM.

摘要

上皮样胶质母细胞瘤(E-GBM)是胶质母细胞瘤(GBM)的一种罕见变体,其特征是上皮样细胞,具有嗜酸性圆形细胞质,无星状细胞质突起。多项研究表明,超过半数的E-GBM在丝氨酸/苏氨酸蛋白激酶BRAF的第600位存在缬氨酸到谷氨酸的替代(BRAF V600E)。然而,此前尚无关于除BRAF V600E突变外还伴有端粒酶逆转录酶(TERT)启动子突变的E-GBM的报道。在此,我们报告一例18岁男性的E-GBM病例,其存在BRAF V600E和TERT启动子突变。肿瘤由80%的E-GBM和20%的弥漫性星形细胞瘤样成分组成,二者均检测到BRAF V600E和TERT启动子突变。E-GBM通常作为原发性病变出现;然而,之前有少数病例显示伴有低级别区域。在低级别和高级别病变中同时出现BRAF V600E和TERT启动子突变,强烈提示它们起源相同,且每个突变可能都是早期事件,可能在E-GBM的发生及随后进展中起关键作用。

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