Glial differentiation in medulloblastoma. Case report.

Neuropatologia polska Pub Date : 1993-01-01
H Kroh, J Bidziński
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Abstract

A 30-year-old man suffered for a year of a typical syndrome of cerebellar tumor. At suboccipital craniectomy a soft tumor infiltrating both hemispheres and vermis, filling up part of the IV ventricle was found. After subtotal removal of the neoplasm the postoperative course was poor and the patient died 5 weeks later. Biopsy material consisted of three types of tissue: 1. large nests of carrot-shaped, hyperchromatic cells, 2. fields of "halo" cells presenting myelin basic protein (MBP) immunoreactivity and 3. fields and scattered strongly GFAP-positive cells. The histological and immunocytochemical pattern of the neoplasm indicates differentiation of the tumor into oligodendrogliomatous and astrocytomatous line being an uncommon example of dual glial differentiation capability in medulloblastoma.

髓母细胞瘤的神经胶质分化。病例报告。
一名30岁的男子患有典型的小脑肿瘤综合征一年。在枕下颅骨切除术中发现一软性肿瘤浸润双脑半球和蚓部,填充部分IV脑室。肿瘤次全切除后病程不佳,患者于5周后死亡。活检材料包括三种类型的组织:1。胡萝卜形的大巢,深染的细胞,2。“晕”细胞呈现髓鞘碱性蛋白(MBP)免疫反应性和3。和分散的强gap阳性细胞。肿瘤的组织学和免疫细胞化学模式表明肿瘤分化为少突胶质细胞瘤和星形细胞瘤系,这是髓母细胞瘤双胶质分化能力的罕见例子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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