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伴有颞下窝扩展的胶质肉瘤。病例报告。

Gliosarcoma with infratemporal fossa extension. Case report.

作者信息

Sade Burak, Prayson Richard A, Lee Joung H

机构信息

Brain Tumor Institute, and Department of Neurosurgery, The Cleveland Clinic Foundation, Cleveland, Ohio 44195, USA.

出版信息

J Neurosurg. 2006 Dec;105(6):904-7. doi: 10.3171/jns.2006.105.6.904.

DOI:10.3171/jns.2006.105.6.904
PMID:17405263
Abstract

Gliosarcomas are bimorphic intraaxial tumors. Involvement of the skull base is highly unexpected. The authors present the case of a temporal lobe gliosarcoma with significant infratemporal fossa extension. This 55-year-old man presented with a 1-month history of severe progressive headache. Neurological examination was unremarkable except for bilateral papilledema. Magnetic resonance imaging revealed a 6-cm right temporal mass with extension into the infratemporal fossa. The patient underwent a right frontotemporal craniotomy together with drilling of the sphenoid ridge and middle fossa floor. The tumor consisted of intraaxial, intracranial as well as extradural, and extracranial components with extension to the posterolateral wall of the sphenoid sinus. It had a relatively well-circumscribed dissection plane. Gross-total resection was achieved, and the middle fossa floor was reconstructed using a rotated temporalis muscle flap. The postoperative course was uneventful except for hypesthesia in the distribution of the maxillary division of the right trigeminal nerve. The histopathological diagnosis was consistent with gliosarcoma. Radiotherapy and chemotherapy consisting of temozolomide were administered subsequently, and the patient was recurrence free 12 months after his initial diagnosis. In the presence of a mass lesion with both intraaxial and extracranial involvement, gliosarcoma should be considered among the differential diagnoses. Aggressive resection should be attempted, including the use of skull base surgical techniques to ensure an optimal outcome. The effect of skull base involvement to the overall treatment and outcome of patients with gliosarcomas would be difficult to determine given the rare occurrence of these lesions in such locations.

摘要

胶质肉瘤是双相性轴内肿瘤。累及颅底非常罕见。作者报告了一例颞叶胶质肉瘤并伴有显著的颞下窝扩展的病例。该55岁男性有1个月严重进行性头痛病史。神经系统检查除双侧视乳头水肿外无异常。磁共振成像显示右侧颞叶有一个6厘米的肿块并延伸至颞下窝。患者接受了右额颞开颅手术,同时磨除蝶骨嵴和中颅窝底。肿瘤由轴内、颅内以及硬膜外和颅外成分组成,并延伸至蝶窦后外侧壁。其有一个相对界限清楚的分离平面。实现了肉眼下全切,并用旋转颞肌瓣重建了中颅窝底。术后过程顺利,除了右侧三叉神经上颌支分布区感觉减退。组织病理学诊断符合胶质肉瘤。随后给予了放疗和替莫唑胺化疗,患者在初次诊断后12个月无复发。在存在既有轴内又有颅外受累的肿块病变时,胶质肉瘤应列入鉴别诊断之中。应尝试积极切除,包括使用颅底外科技术以确保最佳结果。鉴于这些病变在该部位罕见,颅底受累对胶质肉瘤患者总体治疗和预后的影响难以确定。

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