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一名成年患者的BRAF V600E突变型弥漫性胶质瘤:病例报告及文献复习

BRAF V600E-mutated diffuse glioma in an adult patient: a case report and review.

作者信息

Suzuki Yuta, Takahashi-Fujigasaki Junko, Akasaki Yasuharu, Matsushima Satoshi, Mori Ryosuke, Karagiozov Kostadin, Joki Tatsuhiro, Ikeuchi Satoshi, Ikegami Masahiro, Manome Yoshinobu, Murayama Yuichi

机构信息

Department of Neurosurgery, The Jikei University School of Medicine, Tokyo, Japan.

Department of Neuropathology, Brain Bank for Aging Research, Tokyo Metropolitan Institute of Gerontology, 35-2 Sakae-cho, Itabashi-ku, Tokyo, 173-0015, Japan.

出版信息

Brain Tumor Pathol. 2016 Jan;33(1):40-9. doi: 10.1007/s10014-015-0234-4. Epub 2015 Oct 7.

Abstract

Recent advances in genomic technology and genome-wide analysis have identified key molecular alterations that are relevant to the diagnosis and prognosis of brain tumors. Molecular information such as mutations in isocitrate dehydrogenase (IDH) genes or 1p/19q co-deletion status will be more actively incorporated into the histological classification of diffuse gliomas. BRAF V600E mutations are found frequently in circumscribed low-grade gliomas such as pleomorphic xanthoastrocytoma (PXA) and extra-cerebellar pilocytic astrocytoma, or epithelioid glioblastomas (E-GBM), a rare variant of GBM. This mutation is relatively rare in other types of diffuse gliomas, especially in adult onset cases. Here, we present an adult onset case of IDH wild-type/BRAF V600E-mutated diffuse glioma, evolving from grade III to grade IV. The tumor displayed atypical exophytic growth and had unusual histological features not fully compatible with, but indicative of PXA and E-GBM. We discuss differential diagnosis of the tumor, and review previously described diffuse gliomas with the BRAF V600E mutation.

摘要

基因组技术和全基因组分析的最新进展已经确定了与脑肿瘤诊断和预后相关的关键分子改变。诸如异柠檬酸脱氢酶(IDH)基因突变或1p/19q共缺失状态等分子信息将更积极地纳入弥漫性胶质瘤的组织学分类中。BRAF V600E突变常见于局限性低级别胶质瘤,如多形性黄色星形细胞瘤(PXA)和小脑外毛细胞型星形细胞瘤,或胶质母细胞瘤的一种罕见变体——上皮样胶质母细胞瘤(E-GBM)。这种突变在其他类型的弥漫性胶质瘤中相对少见,尤其是在成人发病的病例中。在此,我们报告一例成人发病的IDH野生型/BRAF V600E突变的弥漫性胶质瘤病例,该肿瘤从III级进展为IV级。肿瘤表现为非典型的外生性生长,具有与PXA和E-GBM不完全相符但提示其特征的异常组织学特征。我们讨论了该肿瘤的鉴别诊断,并回顾了先前描述的具有BRAF V600E突变的弥漫性胶质瘤。

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