[A case of desmoplastic infantile ganglioglioma].

M Tadokoro, T Ozawa, M Abe, T Shinagawa, T Sakurai, Y Taguchi
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引用次数: 0

Abstract

We have been experienced a rare case of large supratentorial neuroepithelial tumor with a subdural cyst originated from the left fronto-parietal lobe in a 14-month-old boy. The tumor was characterized by its voluminous size, a leptomeningeal growth pattern with intense desmoplasia and divergent astrocytic and ganglionic differentiation. Schwann cell differentiation and melanocytes were also minutely demonstrated. These histological findings are characteristic of desmoplastic infantile gangliogliomas, reported by VandenBerg et al in 1987. And this tumor tissue architecture strongly suggests the hamartomatous nature, rather than the ordinary neoplastic lesion.

[婴儿结缔组织增塑型神经节胶质瘤1例]。
我们有一例罕见的大幕上神经上皮肿瘤合并硬膜下囊肿起源于左侧额顶叶的14个月大的男孩。肿瘤的特点是体积大,薄脑膜生长模式,伴有强烈的结缔组织增生,星形细胞和神经节分化。雪旺细胞分化和黑素细胞也得到了详细的证实。VandenBerg等人在1987年报道,这些组织学发现是婴儿结缔组织增生神经节胶质瘤的特征。这种肿瘤组织结构强烈提示错构瘤的性质,而不是普通的肿瘤病变。
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