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[一例以颞叶癫痫为表现的大脑外侧裂深部脑膜瘤]

[A case of deep sylvian meningioma presenting temporal lobe epilepsy].

作者信息

Matsumoto S, Yamamoto T, Ban S, Sato S, Shingu T, Yoshida S, Tokuno T, Nakazawa K, Saiwai S, Shirane H

机构信息

Department of Neurosurgery, Kobe City General Hospital, Japan.

出版信息

No To Shinkei. 1995 May;47(5):503-8.

PMID:7786628
Abstract

A rare case of deep sylvian meningioma is presented. A 62-year-old woman was admitted to our hospital because of one year history of temporal lobe epilepsy. She had no neurological deficit except for EEG abnormality. CT scans showed a small calcified mass in the left temporal lobe adjacent to the sylvian fissure with no enhancement by contrast medium. The mass was low-intense in both T1- and T2-weighted MR images. The T1-weighted image after the infusion of gadolinium revealed enhancement of the middle cerebral artery adjacent to the mass, similar to dural tail sign. Left external carotid angiography did not show any tumor stain nor the dilatation of the middle meningeal artery. Left internal carotid angiography disclosed enlarged middle cerebral artery without tumor stain. A left frontotemporal craniotomy was performed and the mass was totally removed. The tumor was located deep in sylvian fissure without any connection to the dura or ventricular system, which was firmly adherent to the middle cerebral artery. The histological examination of the surgical specimen revealed a psammomatous meningioma. Meningiomas are believed to originate from the arachnoid cap cells and can arise from various intracranial locations where arachnoid cap cells exist. The majority of them are attached to the dura, choroid plexus, or the tela choroidea. Only eleven cases of deep sylvian meningiomas have been presented in the literature. We have reviewed the clinical and radiological findings in such meningiomas. MR findings in deep sylvian meningioma have not been described.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本文报告一例罕见的大脑外侧裂深部脑膜瘤。一名62岁女性因颞叶癫痫病史1年入住我院。除脑电图异常外,她无神经功能缺损。CT扫描显示左侧颞叶靠近大脑外侧裂处有一小的钙化肿块,增强造影剂后无强化。该肿块在T1加权和T2加权磁共振图像上均呈低信号。注射钆后T1加权图像显示肿块附近大脑中动脉强化,类似于脑膜尾征。左侧颈外动脉造影未显示任何肿瘤染色,也未显示脑膜中动脉扩张。左侧颈内动脉造影显示大脑中动脉增粗,无肿瘤染色。行左侧额颞开颅术,肿瘤被完全切除。肿瘤位于大脑外侧裂深部,与硬脑膜或脑室系统无任何连接,紧密附着于大脑中动脉。手术标本的组织学检查显示为砂粒型脑膜瘤。脑膜瘤被认为起源于蛛网膜帽细胞,可发生于存在蛛网膜帽细胞的各种颅内部位。大多数脑膜瘤附着于硬脑膜、脉络丛或脉络膜组织。文献中仅报道了11例大脑外侧裂深部脑膜瘤。我们回顾了此类脑膜瘤的临床和影像学表现。大脑外侧裂深部脑膜瘤的磁共振表现尚未见描述。(摘要截短至250字)

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