Maruyama R, Koga K, Nakahara T, Kishida K, Nabeshima K
Department of Central Laboratory, Nobeoka Prefectural Hospital, Miyazaki, Japan.
Hum Pathol. 1992 Aug;23(8):960-2. doi: 10.1016/0046-8177(92)90413-w.
A rare case of myxopapillary ependymoma is reported. The tumor occurred in the cerebral hemisphere of an 8-year-old girl and had no relationship to the lateral ventricles. Microscopically, it showed abundant mucin production around papillary or reticular structures. Immunohistochemically, these tumor cells were weakly positive, with glial fibrillary acidic protein demonstrated in part of the tumor and vimentin strongly demonstrated throughout the tumor. The results may indicate the poorly differentiated nature of this tumor. This is the second reported case of intracranial myxopapillary ependymoma.
报告了一例罕见的黏液乳头型室管膜瘤。该肿瘤发生于一名8岁女孩的脑半球,与侧脑室无关。显微镜下,肿瘤在乳头或网状结构周围可见大量黏液分泌。免疫组化显示,这些肿瘤细胞呈弱阳性,部分肿瘤细胞表达胶质纤维酸性蛋白,波形蛋白在整个肿瘤中均呈强阳性表达。这些结果可能提示该肿瘤分化较差。这是第二例颅内黏液乳头型室管膜瘤的报道病例。