Bilateral rhabdoid meningioma mimicking glioma: an unusual occurrence.

Q1 Medicine
GMS German Medical Science Pub Date : 2017-08-14 eCollection Date: 2017-01-01 DOI:10.3205/000253
Varsha Dalal, Fouzia Siraj, Manveen Kaur, K B Shankar, Avninder Singh
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引用次数: 2

Abstract

Rhabdoid meningioma is an infrequent variant of meningioma, introduced for the first time in the 2000 World Health Organization's classification of tumors of the nervous system. Owing to its aggressive clinical course and high proliferative index, it has been classified as a grade III neoplasm. We describe a fifty-year-old male with headache, weakness of limbs, and altered sensorium. CT showed hetero-dense enhancing mass lesions in both right and left parietal areas raising suspicion of high grade glioma. Histopathologic and immunohistochemical examination revealed a tumor with features of rhabdoid meningioma. A review of literature did not reveal any bilateral occurrence of this tumor.

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双侧模拟神经胶质瘤横纹肌样脑膜瘤:罕见病例。
横纹肌样脑膜瘤是脑膜瘤的一种罕见变体,在2000年世界卫生组织对神经系统肿瘤的分类中首次被引入。由于其侵袭性的临床过程和高增殖指数,它已被归类为III级肿瘤。我们描述一个五十岁的男性头痛,四肢无力,和改变感觉。CT示左右顶骨区异密度增强肿块,怀疑为高级别胶质瘤。组织病理及免疫组化检查显示为横纹肌样脑膜瘤。文献回顾未发现任何双侧肿瘤的发生。
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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来源期刊
GMS German Medical Science
GMS German Medical Science Medicine-Medicine (all)
CiteScore
6.30
自引率
0.00%
发文量
10
审稿时长
11 weeks
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