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腹腔原发性恶性室管膜瘤:一例报告并文献复习

A primary malignant ependymoma of the abdominal cavity: a case report and review of the literature.

作者信息

Mogler Carolin, Kohlhof Patricia, Penzel Roland, Grenacher Lars, Haag Georg M, Schirmacher Peter, Mueller Wolf

机构信息

Department of General Pathology, University Hospital, Heidelberg, Germany.

出版信息

Virchows Arch. 2009 Apr;454(4):475-8. doi: 10.1007/s00428-009-0744-8. Epub 2009 Feb 24.

Abstract

Ependymomas generally arise in the central nervous system (CNS). Rare primary extraneural ependymomas have been observed. Here, we describe the first case of an overt malignant primary extraneural ependymoma in a young female patient. Careful reevaluation together with extensive review of the literature and comparison of related cases established the diagnosis after treatment failure and tumor progression. The tumor was large and firm with some small cysts and showed pseudorosettes with strong glial fibrillary acidic protein (GFAP) expression. In conclusion, primary extraneural ependymomas have to be included into the differential diagnosis of abdominal tumors with pseudorosette-formation, even in unusual sites, and GFAP-immunohistochemistry (IHC) supports the diagnosis.

摘要

室管膜瘤通常起源于中枢神经系统(CNS)。已观察到罕见的原发性神经外室管膜瘤。在此,我们描述了一名年轻女性患者中首例明显的恶性原发性神经外室管膜瘤。在治疗失败和肿瘤进展后,通过仔细的重新评估以及对文献的广泛回顾和相关病例的比较得以确诊。肿瘤体积大且质地硬,伴有一些小囊肿,显示假菊形团,胶质纤维酸性蛋白(GFAP)表达强烈。总之,即使在不寻常的部位,原发性神经外室管膜瘤也必须纳入具有假菊形团形成的腹部肿瘤的鉴别诊断中,并且GFAP免疫组织化学(IHC)有助于诊断。

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