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首页> 外文期刊>Clinical neuropathology >A neuroepithelial tumor showing combined histological features of dysembryoplastic neuroepithelial tumor and pleomorphic xanthoastrocytoma--a case report and review of the literature.
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A neuroepithelial tumor showing combined histological features of dysembryoplastic neuroepithelial tumor and pleomorphic xanthoastrocytoma--a case report and review of the literature.

机译:一种神经上皮肿瘤,表现出发育不良的神经上皮肿瘤和多形性黄体星形细胞瘤的组织学特征-一例病例并文献复习。

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摘要

A neuroepithelial tumor showing combined histological features of dysembryoplastic neuroepithelial tumor (DNT) and pleomorphic xanthoastrocytoma (PXA) is described. The patient was a 60-year-old male with a long-standing temporal lobe tumor and seizures. After a long, dormant period, the tumor, which had been localized in the left uncus, re-grew rapidly and extended into the subarachnoidal space and brain stem. The post-operative specimens disclosed two distinct components: an intra-cortical, cystic lesion containing mucinous materials and an extra-cortical, nodular lesion involving the leptomeninges. The former contained oligodendroglia-like small, round cells placed along axonal processes, plus mature neurons situated against mucinous materials (DNT-like component, WHO Grade I). The latter contained spindle and/or pleomorphic cells expressing glial fibrillary acidic protein, having bizarre nuclei and atypical mitotic figures. A reticulin network was developed among the tumor cells (PXA-like component, WHO Grade III). This case illustrates an unusual composite brain tumor, combined DNT and PXA.
机译:描述了一种神经上皮肿瘤,表现出发育不良的神经上皮肿瘤(DNT)和多形性黄体星形细胞瘤(PXA)的联合组织学特征。该患者是一名60岁的男性,患有长期的颞叶肿瘤和癫痫发作。经过长时间的潜伏期后,原本位于左un骨中的肿瘤迅速长大并扩展到蛛网膜下腔和脑干。术后标本揭示了两个截然不同的组成部分:皮质内的囊性病变包含粘液物质,皮质外的结节性病变累及软脑膜。前者包含沿着轴突过程放置的少突胶质细胞样小圆形细胞,以及位于粘液质物质(DNT样成分,WHO等级I)上的成熟神经元。后者包含表达神经胶质原纤维酸性蛋白的纺锤状和/或多形性细胞,具有奇异的核和非典型的有丝分裂图。在肿瘤细胞之间建立了网状蛋白网络(PXA样成分,WHO III级)。该病例说明了一种罕见的复合性脑肿瘤,DNT和PXA联合治疗。

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