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多形性黄色星形细胞瘤:两例报告

Pleomorphic xanthoastrocytoma: a report of two cases.

作者信息

Jones M C, Drut R, Raglia G

出版信息

Pediatr Pathol. 1983 Oct-Dec;1(4):459-67. doi: 10.3109/15513818309025878.

Abstract

We report two cases of a recently isolated variety of astrocytoma, pleomorphic xanthoastrocytoma, affecting the cerebral cortex and meninges of children and young adults. The first tumor was localized in the left frontal lobe of a 9-year-old girl. The second appeared in the right parietal lobe of a 14-year-old girl. Both tumors displayed a pleomorphic cellular proliferation, with spindle-shaped and bizarre multinucleated giant cells, some positive for neutral lipids, with a prominent reticulin network and areas highly suggestive of malignant fibrohistiocytomas (fibroxanthosarcomas). The glial fibrillary acidic protein was demonstrated by the immunoperoxidase method in the cytoplasm of the giant and the spindle cells. Ultrastructural studies confirmed the glial nature of the tumor. This type of tumor seems to carry a much better prognosis than other tumors from which it has to be separated, e.g., glioblastoma and meningeal sarcomas.

摘要

我们报告了两例最近分离出的星形细胞瘤变种——多形性黄色星形细胞瘤,其累及儿童和年轻成人的大脑皮层和脑膜。第一例肿瘤位于一名9岁女孩的左额叶。第二例出现在一名14岁女孩的右顶叶。两例肿瘤均显示多形性细胞增殖,有梭形和奇异的多核巨细胞,部分细胞中性脂质呈阳性,有明显的网状纤维网络,且有高度提示恶性纤维组织细胞瘤(纤维黄色肉瘤)的区域。通过免疫过氧化物酶法在巨细胞和梭形细胞的胞质中证实了胶质纤维酸性蛋白的存在。超微结构研究证实了肿瘤的胶质性质。这种类型的肿瘤似乎比其他需要与之鉴别的肿瘤,如胶质母细胞瘤和脑膜肉瘤,预后要好得多。

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