横纹肌样脑膜瘤以不典型脑膜瘤伴脂肪瘤化生为背景:1例报告及文献复习

S. Shuja, T. Lucey, Victor R. Dasilva, Raafat Maakary
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引用次数: 0

摘要

脑膜瘤在组织学上是异质性的,大多数组织学亚型没有预后意义,被WHO列为1级。临床上复发风险增加的患者被WHO列为II级或III级。新近加入脑膜瘤家族的是一种称为横纹肌样脑膜瘤的罕见变异,它与复发风险增加和侵袭性临床行为相关,因此被WHO列为III级脑膜瘤。我们报告一个43岁男性横纹肌样脑膜瘤的病例,在不典型脑膜瘤的背景下,表现出横纹肌样和脂肪瘤成分的不寻常组合。本文描述了该病例的临床特征、神经影像学、手术治疗结果和病理特征,并对有关患者预后和治疗方案的文献进行了有限的回顾。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rhabdoid Meningioma In A Background Of Atypical Meningioma With Lipomatous Metaplasia: Case Report And Review Of Literature
Meningiomas are heterogenous in their histology, and most of histologic subtypes have no prognostic significance, and are classified as WHO grade 1. Those with clinically increased risk of recurrence are classified as WHO grade II or III. A relatively recent addition to the meningioma family is a rare variant called rhabdoid meningioma, which is associated with increased risk of recurrence and aggressive clinical behavior and therefore classified as WHO grade III meningioma. We report a case of rhabdoid meningioma in a 43 year old man, which exhibited an unusual combination of rhabdoid and lipomatous components, in a background of atypical meningioma. The clinical features, neuroimaging, surgical treatment results and pathological features of this case are described with a limited review of literature regarding prognosis of patients and treatment options.
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