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颞叶肿瘤显示神经节胶质瘤和多形性黄色星形细胞瘤成分。病例报告。

Temporal lobe tumor demonstrating ganglioglioma and pleomorphic xanthoastrocytoma components. Case report.

作者信息

Furuta A, Takahashi H, Ikuta F, Onda K, Takeda N, Tanaka R

机构信息

Department of Pathology, Niigata University, Japan.

出版信息

J Neurosurg. 1992 Jul;77(1):143-7. doi: 10.3171/jns.1992.77.1.0143.

Abstract

The case is reported of a 16-year-old boy with a left temporal lobe tumor composed of a ganglioglioma and a pleomorphic xanthoastrocytoma. Histologically, the tumor had two different components. One component involved the cortex of the left posterior temporal lobe and showed an aggregation of neuronal cells with an astroglial stroma. Ultrastructurally, numerous dense-cored vesicles, diagnosed as ganglioglioma, were found in the neuronal cells. The other component involved the adjacent cortex and white matter of the left anterior temporal lobe and the surrounding subarachnoid space. This was composed of pleomorphic cells with many multinucleated giant cells and occasional foamy cells. Most of the tumor cells were positive for glial fibrillary acidic protein. These features correspond well to earlier descriptions of pleomorphic xanthoastrocytoma. At 24 months following total tumor extirpation, the patient is alive and has had no evidence of tumor recurrence.

摘要

报告了一例16岁男孩,其左颞叶肿瘤由神经节胶质瘤和多形性黄色星形细胞瘤组成。组织学上,肿瘤有两种不同成分。一种成分累及左颞叶后部皮质,表现为神经元细胞聚集并伴有星形胶质细胞基质。超微结构上,在神经元细胞中发现大量致密核心小泡,诊断为神经节胶质瘤。另一种成分累及左颞叶前部相邻皮质、白质及周围蛛网膜下腔。它由多形性细胞组成,有许多多核巨细胞和偶见的泡沫细胞。大多数肿瘤细胞胶质纤维酸性蛋白呈阳性。这些特征与多形性黄色星形细胞瘤的早期描述非常相符。肿瘤全切术后24个月,患者存活,无肿瘤复发迹象。

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