Kuhajda F P, Mendelsohn G, Taxy J B, Long D M
Department of Pathology, The Johns Hopkins University School of Medicine and Hospital, Baltimore, Maryland 21205, USA.
Ultrastruct Pathol. 1981 Jan-Mar;2(1):25-32. doi: 10.3109/01913128109031500.
A case of pleomorphic xanthoastrocytoma is reported with light and electron microscopic findings. This unusual tumor arose in a 15-year-old male. The tumor consisted predominantly of nests of xanthomatous cells and plump spindle cells surrounded by a prominent reticulin network. There was considerable cellular pleomorphism with abundant bizarre giant cells and multinucleated cells. Occasional mitoses were present. Electron microscopy and immunoperoxidase localization of glial fibrillary acidic protein (GFAP) confirmed the glial nature of the tumor. Recognition of this tumor is important. Despite its "m alignant" appearance, the tumor characteristically has a relatively good prognosis and should not be confused with high-grade gliomas or meningeal sarcomas, which require aggressive therapy.
报告了一例多形性黄色星形细胞瘤的光镜和电镜检查结果。该罕见肿瘤发生于一名15岁男性。肿瘤主要由黄色瘤细胞巢和丰满的梭形细胞组成,周围有明显的网状纤维网络。存在显著的细胞多形性,有大量奇异的巨细胞和多核细胞。可见散在的有丝分裂象。电镜检查和胶质纤维酸性蛋白(GFAP)免疫过氧化物酶定位证实了肿瘤的胶质性质。认识这种肿瘤很重要。尽管其外观呈“恶性”,但该肿瘤通常预后相对较好,不应与需要积极治疗的高级别胶质瘤或脑膜肉瘤相混淆。