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[1例伴有明显颅外扩展的三叉神经鞘瘤]

[A case of trigeminal neurinoma with marked extracranial extension].

作者信息

Fushimi S, Miura S, Suda Y, Fujii S, Kowada M

机构信息

Neurosurgical Service, Akita University Hospital, Japan.

出版信息

No Shinkei Geka. 1987 Oct;15(10):1117-22.

PMID:3323932
Abstract

A case of trigeminal neurinoma with marked extracranial extension is reported with a review of the literature. A 60-year-old female noticed numbness over the left side of the face during the proceeding 15 years. Two years prior to admission, she began to complain of itching and lancinating pain at the left lateral aspect of the nose. Neurologic examination on admission revealed diminished corneal reflex on the left side and hypesthesia in the distribution of the left trigeminal nerve. There was no weakness or atrophy of the ipsilateral masticatory muscles. The remaining cranial nerves and cerebellar functions were normal. Craniograms showed destruction of the left petrous apex, enlargement of the left superior orbital fissure and an extensive bone defect in the floor of the left middle cranial fossa. CT disclosed a huge heterogeneously enhancing mass lesion in the left middle cranial fossa, which extended posteriorly into the left cerebellopontine angle and inferiorly into the pterygoid and infratemporal fossae. Cerebral angiograms revealed medial displacement of the left internal cerebral artery in the ganglionic, cavernous and supraclinoid portions, and elevation of the left middle cerebral artery in the sphenoidal portion. Although the left meningohypophyseal trunk was dilated, no tumor stain was observed. A transantral biopsy specimen provided the diagnosis of neurinoma with Antoni type A tissue. The patient was followed up at the outpatient clinic as radical operations were not agreed upon. Eight cases of trigeminal neurinoma with extracranial extension are reviewed including the presented case. There were two males and six females, and the age varied from 16 to 65 years.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本文报告一例伴有明显颅外扩展的三叉神经鞘瘤,并对相关文献进行综述。一名60岁女性在过去15年中逐渐出现左侧面部麻木。入院前两年,她开始抱怨左侧鼻翼外侧瘙痒和刺痛。入院时神经系统检查发现左侧角膜反射减弱,左侧三叉神经分布区域感觉减退。同侧咀嚼肌无无力或萎缩。其余颅神经和小脑功能正常。颅骨X线片显示左侧岩尖骨质破坏,左侧眶上裂扩大,左侧中颅窝底有广泛骨缺损。CT显示左侧中颅窝有一个巨大的不均匀强化肿块,向后延伸至左侧桥小脑角,向下延伸至翼腭窝和颞下窝。脑血管造影显示左侧大脑中动脉在神经节、海绵窦和鞍上部分向内移位,在蝶骨部分向上抬高。虽然左侧脑膜垂体干增粗,但未观察到肿瘤染色。经鼻窦活检标本诊断为具有Antoni A型组织的神经鞘瘤。由于患者不同意接受根治性手术,故在门诊进行随访。本文回顾了包括该病例在内的8例伴有颅外扩展的三叉神经鞘瘤。其中男性2例,女性6例,年龄在16至65岁之间。(摘要截短至250字)

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