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皮下骶尾部黏液乳头型室管膜瘤。病例报告及文献复习。

Subcutaneous sacrococcygeal myxopapillary ependymoma. A case report and review of the literatures.

作者信息

Matsuo K, Kumagai K, Kawai K, Tsuchiyama H

出版信息

Acta Pathol Jpn. 1985 Jul;35(4):925-31. doi: 10.1111/j.1440-1827.1985.tb00634.x.

Abstract

A case of myxopapillary ependymoma originating in the soft tissue is described. The tumor was located subcutaneously over the coccyx of an 11-year-old girl but was connected neither to the filum terminale nor cauda equina. Clinically, the tumor was locally resected with a diagnosis of pilonidal cyst. Histological and electron microscopic findings were identical to myxopapillary ependymoma. The tumor cells showed a positive reaction by immunoperoxidase method (PAP method) of glial fibrillary acidic protein (GFAP).

摘要

本文描述了一例起源于软组织的黏液乳头状室管膜瘤。该肿瘤位于一名11岁女孩尾骨皮下,但与终丝及马尾均无连接。临床上,该肿瘤被诊断为藏毛囊肿并进行了局部切除。组织学和电子显微镜检查结果与黏液乳头状室管膜瘤一致。肿瘤细胞经胶质纤维酸性蛋白(GFAP)免疫过氧化物酶法(PAP法)检测呈阳性反应。

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