Pimentel J, Kepes J J, Moura Nunes J F, Bentes C, Miguéns J, Antunes J L
Laboratório de Neuropatologia, Hospital de Santa Maria, Lisboa, Portugal.
Clin Neuropathol. 2001 Jan-Feb;20(1):31-7.
Ependymomas account for 3 to 9% of all neuroepithelial tumors and, although occurring most often within the ventricular system, they may arise from the extraventricular parenchyma as well. Several histologic patterns of these neoplasm are well known, but little attention has been devoted to a variant composed of giant elements. We describe the case of a 13-year-old girl experiencing a 3-month history of partial seizures in whom cranial magnetic resonance imaging showed an extraventricular, right parietotemporal neoplasm, adherent to the overlying dura mater. Histologic, immunohistochemical and ultrastructural findings were consistent with those of a high-grade ependymoma. The tumor was characterized by the presence of a major component of pleomorphic giant cells, as also seen in pleomorphic xantoastrocytoma, subependymal giant cell astrocytoma and glioblastoma multiforme. Similar elements have been described in two filum terminale and one supratentorial, intraventricular ependymoma, respectively. Histologic and evolutional data of those and of our own case suggest that isolated giant cells are not necessarily linked to a bad prognosis in ependymomas.
室管膜瘤占所有神经上皮肿瘤的3%至9%,尽管最常发生于脑室系统内,但也可起源于脑室外实质。这些肿瘤的几种组织学模式已为人熟知,但对一种由巨大细胞组成的变体关注较少。我们描述了一名13岁女孩的病例,她有3个月的部分性癫痫病史,头颅磁共振成像显示脑室外右顶颞部肿瘤,与硬脑膜粘连。组织学、免疫组化和超微结构检查结果与高级别室管膜瘤相符。该肿瘤的特征是存在多形性巨细胞的主要成分,这在多形性黄色星形细胞瘤、室管膜下巨细胞星形细胞瘤和多形性胶质母细胞瘤中也可见到。分别在两个终丝和一个幕上脑室室管膜瘤中也描述过类似成分。那些病例以及我们自己病例中的组织学和演变数据表明,在室管膜瘤中,孤立的巨细胞不一定与不良预后相关。