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桥小脑角区影像学表现难以区分的脑膜瘤与前庭神经鞘瘤并存的罕见病例——病例报告及文献综述

A Rare Case of Radiologically Not Distinguishable Coexistent Meningioma and Vestibular Schwannoma in the Cerebellopontine Angle - Case Report and Literature Review.

作者信息

Grauvogel Juergen, Grauvogel Tanja Daniela, Taschner Christian, Baumgartner Sandra, Maier Wolfgang, Kaminsky Jan

机构信息

Department of Neurosurgery, Albert-Ludwigs-University of Freiburg, Freiburg, Germany.

出版信息

Case Rep Neurol. 2010 Aug 27;2(2):111-117. doi: 10.1159/000320213.

DOI:10.1159/000320213
PMID:21045938
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2968772/
Abstract

BACKGROUND

The simultaneous occurrence of cerebellopontine angle (CPA) meningioma and vestibular schwannoma (VS) in the absence of neurofibromatosis type 2 or history of irradiation is very rare. We report a case with coexistent CPA meningioma and VS, which were radiologically not distinguishable in preoperative imaging. CASE DESCRIPTION: A 46-year-old female presented with acute hearing loss, tinnitus and gait ataxia. Otorhinolaryngological diagnostic workup and imaging studies showed an intra- and extrameatal homogenous contrast enhancing lesion. The neuroradiological diagnosis was VS. The patient was operated via the retrosigmoid approach. INTRAOPERATIVELY TWO DISTINCT TUMORS WERE FOUND: a small, mainly intrameatally located VS and a larger meningioma originating from the dura of the petrous bone. Both tumors were completely microsurgically removed. The patient experienced no new neurological deficit after surgery; particularly facial nerve function was completely preserved. Histopathological examination revealed a fibromatous meningioma and a VS, respectively. CONCLUSIONS: The coincidental occurrence of CPA meningioma and VS is very rare. Careful interpretation of imaging studies before surgery is crucial. Even such rare cases should be kept in mind when discussing the therapeutic options with the patient. More studies are needed for a better understanding of mechanisms leading to multiple tumor growth.

摘要

背景

在无2型神经纤维瘤病或放疗史的情况下,同时发生小脑桥脑角(CPA)脑膜瘤和前庭神经鞘瘤(VS)非常罕见。我们报告一例CPA脑膜瘤和VS并存的病例,术前影像学检查在放射学上无法区分这两种肿瘤。病例描述:一名46岁女性,出现急性听力丧失、耳鸣和步态共济失调。耳鼻喉科诊断检查和影像学研究显示,耳道内和耳道外有均匀强化的病变。神经放射学诊断为VS。患者通过乙状窦后入路进行手术。术中发现两个不同的肿瘤:一个小的、主要位于耳道内的VS和一个起源于岩骨硬脑膜的较大脑膜瘤。两个肿瘤均通过显微手术完全切除。患者术后未出现新的神经功能缺损;尤其是面神经功能完全保留。组织病理学检查分别显示为纤维瘤性脑膜瘤和VS。结论:CPA脑膜瘤和VS同时发生非常罕见。术前仔细解读影像学检查至关重要。在与患者讨论治疗方案时,即使是这种罕见病例也应予以考虑。需要更多研究以更好地理解导致多发肿瘤生长的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e22a/2968772/70a7b736dcea/crn0002-0111-f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e22a/2968772/5784da8765af/crn0002-0111-f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e22a/2968772/73052d6ef06e/crn0002-0111-f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e22a/2968772/70a7b736dcea/crn0002-0111-f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e22a/2968772/5784da8765af/crn0002-0111-f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e22a/2968772/73052d6ef06e/crn0002-0111-f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e22a/2968772/70a7b736dcea/crn0002-0111-f03.jpg

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