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颈段脊髓巨细胞型室管膜瘤:病例报告及文献复习

Giant cell ependymoma of the cervical spinal cord: case report and review of the literature.

作者信息

Barbagallo Giuseppe M V, Caltabiano Rosario, Parisi Giuseppe, Albanese Vincenzo, Lanzafame Salvatore

机构信息

Department of Neurosurgery, Azienda Ospedaliero-Universitaria Policlinico G. Rodolico, Catania, Italy.

出版信息

Eur Spine J. 2009 Jul;18 Suppl 2(Suppl 2):186-90. doi: 10.1007/s00586-008-0789-4. Epub 2008 Sep 27.

Abstract

Ependymomas account for 2-6% of all central nervous system neoplasms. They develop from the ependymal cells that line the ventricular cavities of the brain and the central canal of the spinal cord, as well as from ependymal clusters in the filum terminale. Giant cell ependymoma (GCE) is a rare subtype, with few cases reported, mostly in the brain. We describe the case of a cervical spinal cord ependymoma with pleomorphic giant cells and focal calcifications occurring in a 25-year-old woman. Magnetic resonance imaging revealed a large multicystic and partially enhancing intramedullary tumour extending from C2 to C5. Intraoperative analysis of frozen section tissue fragments suggested a malignant tumour; however, an obvious cleavage plane was present around most of the mass, and a macroscopically complete tumour removal could be achieved. Subsequently, paraffin sections and immunohistochemical investigations revealed unequivocal evidence of a GCE with focal calcifications. This case, the second giant-cell ependymoma to be described in the spinal cord and the first with focal calcifications, highlights the features of GCE and the discrepancy between the worrisome histological appearance, the surgical findings and the clinical relatively good prognosis.

摘要

室管膜瘤占所有中枢神经系统肿瘤的2% - 6%。它们起源于衬于脑室内腔和脊髓中央管的室管膜细胞,以及终丝中的室管膜细胞簇。巨细胞室管膜瘤(GCE)是一种罕见的亚型,报道的病例很少,主要发生在脑部。我们描述了一例25岁女性发生的伴有多形性巨细胞和局灶性钙化的颈段脊髓室管膜瘤。磁共振成像显示一个大的多囊性且部分强化的髓内肿瘤,从C2延伸至C5。术中对冰冻切片组织碎片的分析提示为恶性肿瘤;然而,大部分肿块周围存在明显的分离平面,可实现肉眼下肿瘤的完整切除。随后,石蜡切片和免疫组化检查明确显示为伴有局灶性钙化的GCE。该病例是脊髓中描述的第二例巨细胞室管膜瘤,也是首例伴有局灶性钙化的病例,突出了GCE的特征以及令人担忧的组织学表现、手术发现与相对良好的临床预后之间的差异。

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