组蛋白突变胶质瘤表现为弥漫性脑膜轻脑病。

Q1 Medicine CNS Oncology Pub Date : 2021-09-01 DOI:10.2217/cns-2021-0008
Tanvi Nadkarni, Kimberly Hamilton, Faraze Niazi, Melanie Ward, Uchenna Okakpu, Rudolph J Castellani, Ion Prisneac, Ugur Sener
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引用次数: 3

摘要

多形性胶质母细胞瘤是成人最常见的原发性恶性脑肿瘤。组蛋白H3突变已在儿童和成人胶质瘤中被发现,H3K27M突变通常与后窝中线肿瘤位置和预后不良有关。轻脑膜病是已知的组蛋白突变胶质瘤的并发症,但在最初诊断时并不常见。我们描述了一例H3K27M突变的胶质母细胞瘤,该病例最初表现为弥漫性脑脊膜疾病导致的进行性视力丧失,除了小脑小区增强外,没有肿块病变,两次脑脊液细胞学检查均为恶性细胞阴性,强调了在弥漫性脑脊膜增强的鉴别中包括原发性中枢神经系统恶性肿瘤的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Histone-mutant glioma presenting as diffuse leptomeningeal disease.

Glioblastoma multiforme is the most common malignant primary brain tumor in adults. Histone H3 mutations have been identified in pediatric and adult gliomas, with H3K27M mutations typically associated with a posterior fossa midline tumor location and poor prognosis. Leptomeningeal disease is a known complication of histone-mutant glioma, but uncommon at the time of initial diagnosis. We describe a case of glioblastoma with H3K27M mutation that initially presented with progressive vision loss due to diffuse leptomeningeal disease in the absence of a mass lesion other than a small cerebellar area of enhancement and with cerebrospinal fluid cytology negative for malignant cells on two occasions, highlighting the importance of including primary CNS malignancies in the differential of diffuse radiographic leptomeningeal enhancement.

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来源期刊
CNS Oncology
CNS Oncology Medicine-Neurology (clinical)
CiteScore
3.80
自引率
0.00%
发文量
12
审稿时长
13 weeks
期刊最新文献
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