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桥小脑角脑膜瘤合并副神经神经鞘瘤——病例报告

Cerebellopontine angle meningioma associated with cranial accessory nerve neurinoma--case report.

作者信息

Tsukamoto H, Hikita T, Takaki T

机构信息

Department of Neurosurgery, Hamanomachi General Hospital, Fukuoka.

出版信息

Neurol Med Chir (Tokyo). 1994 Apr;34(4):225-9. doi: 10.2176/nmc.34.225.

Abstract

A 46-year-old female presented with a rare association of cerebellopontine (CP) angle meningioma with accessory nerve neurinoma manifesting as headache, occasional diplopia, speech disturbance, swallowing difficulty, and unsteady gait. Magnetic resonance imaging demonstrated a large tumor in the left CP angle. The tumor was totally removed through a lateral suboccipital approach. During the operation another smaller tumor was found originating from the cranial accessory nerve and was also totally removed. Histological examination found that the larger tumor was a meningotheliomatous meningioma and the smaller an Antoni type A neurinoma. The symptoms were apparently due to the larger tumor. Careful examination of neuroimages is necessary even after the main lesions responsible for the symptoms are identified.

摘要

一名46岁女性患者,表现为罕见的桥小脑角(CP)脑膜瘤合并副神经神经鞘瘤,症状包括头痛、偶尔复视、言语障碍、吞咽困难和步态不稳。磁共振成像显示左侧桥小脑角有一个大肿瘤。通过枕下外侧入路将肿瘤完全切除。手术中发现另一个较小的肿瘤起源于颅副神经,也被完全切除。组织学检查发现较大的肿瘤是上皮型脑膜瘤,较小的是Antoni A型神经鞘瘤。症状显然是由较大的肿瘤引起的。即使在确定了导致症状的主要病变后,仔细检查神经影像也是必要的。

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