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[原发性“肌肉”肿瘤或中枢神经系统具有肌肉瘤成分的肿瘤。基于两项解剖学-临床观察的综述及分类尝试]

[Primary "muscle" tumors or tumors with a myosarcomatous component of the central nervous system. General review and attempt at classification based on 2 anatomo-clinical observations].

作者信息

Pasquier B, Couderc P, Pasquier D, Panh M H, Barge M

出版信息

Sem Hop. 1977 Oct 23;53(36):1927-40.

PMID:208159
Abstract

The authors report the first two French cases of primary rabdomyosarcoma of the central nervous system. They then review the literature on muscle tumours or primary myosarcomas of the nervous system of which 29 cases have now been published. From the point of view of morphology and classification, one should distinguish firstly, purely mesenchymatous tumours (rhabdomyosarcomas, leiosarcoma, mesenchymoma) and secondly, composite tumours of connective tissue or spino-epithelial tumours (medullomyoblastomas, neuromyoblastomas, gliomyosarcomas). Their histogenesis occurs from the ectomesenchyme of the neural crests.

摘要

作者报告了法国首例中枢神经系统原发性横纹肌肉瘤的前两例病例。他们随后回顾了关于肌肉肿瘤或神经系统原发性肌肉瘤的文献,目前已发表了29例。从形态学和分类的角度来看,首先应区分纯粹的间充质肿瘤(横纹肌肉瘤、平滑肌肉瘤、间叶瘤),其次是结缔组织复合肿瘤或棘上皮肿瘤(髓母细胞瘤、神经母细胞瘤、胶质肉瘤)。它们的组织发生源自神经嵴的外胚层间充质。

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