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起源于颞顶叶错构瘤样病变的胶质纤维瘤。

Gliofibroma originating from temporoparietal hamartoma-like lesions.

作者信息

Reinhardt V, Nahser H C

出版信息

Clin Neuropathol. 1984 May-Jun;3(3):131-8.

PMID:6565539
Abstract

Clinical and neuropathologic observations are reported of a 16-year-old girl with a right temporoparietal tumor. The histologic picture revealed cortical areas with a peculiar growth of neurons, glia or tumor cells, and strands of collagen following the pattern of the cortical architecture. In this area of hamartoma-like cortex a large tumor nodule was found with anaplastic cells in fibrous stroma exhibiting partially positive GFAP reaction. The picture closely resembles the features of a tumor described in 1978 by Friede in the medulla oblongata of a 3-year and 9-month-old girl. A comparison of histology and ultrastructure of both tumors is followed by discussion of the origin of this peculiar type of tumor, focussing on the existence of unusually pluripotent cells that may develop into glial and mesenchymal cells.

摘要

报告了一名患有右颞顶叶肿瘤的16岁女孩的临床和神经病理学观察结果。组织学图像显示皮质区域有神经元、胶质细胞或肿瘤细胞的特殊生长,以及遵循皮质结构模式的胶原束。在这个错构瘤样皮质区域发现了一个大的肿瘤结节,纤维基质中的间变细胞呈现部分阳性的GFAP反应。该图像与1978年Friede在一名3岁9个月大女孩的延髓中描述的肿瘤特征非常相似。对这两种肿瘤的组织学和超微结构进行比较后,讨论了这种特殊类型肿瘤的起源,重点关注可能发育为胶质细胞和间充质细胞的异常多能细胞的存在。

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