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具有脉络丛分化的原始神经外胚层肿瘤。

Primitive neuroectodermal tumor with choroid plexus differentiation.

作者信息

Janzer R C, Kleihues P

出版信息

Clin Neuropathol. 1985 May-Jun;4(3):93-8.

PMID:2990787
Abstract

A case of a cerebral juvenile undifferentiated round cell tumor with unusual formation of glandular structures is presented. The round cell component showed focal expression of glial fibrillary acidic protein, S-100 protein, neurofilament protein and neuron-specific enolase. The glandular part consisted of papillary epithelial structures with a central PAS-positive lumen. Ultrastructural findings supported the interpretation of these parts as choroid plexus. This route of differentiation was recognizable at the first operation at the age of 5 years and was much more prominent in the recurrence found 7 1/2 years later. The unusually benign course of this primitive neuroectodermal tumor (PNET) may be due to its intrinsic progressive tendency towards choroid plexus differentiation.

摘要

本文报告一例脑青少年未分化圆形细胞瘤,伴有不寻常的腺结构形成。圆形细胞成分显示胶质纤维酸性蛋白、S-100蛋白、神经丝蛋白和神经元特异性烯醇化酶的局灶性表达。腺部分由具有中央PAS阳性管腔的乳头状上皮结构组成。超微结构发现支持将这些部分解释为脉络丛。这种分化途径在5岁首次手术时即可识别,在7年半后发现的复发中更为明显。这种原始神经外胚层肿瘤(PNET)异常良性的病程可能归因于其向脉络丛分化的内在渐进趋势。

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