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中枢神经系统原发性横纹肌肉瘤

Primary rhabdomyosarcoma of the central nervous system.

作者信息

Pasquier B, Couderc P, Pasquier D, Hong P M, Pellat J

出版信息

Acta Neuropathol. 1975 Dec 30;33(4):333-42. doi: 10.1007/BF00686165.

Abstract

A case of primary rhabdomyosarcoma in the brain stem is described in an 8 year old girl. The clinical data showed a right side hemiplegia then a total paralysis of the left sixth cranial nerve and a paraplegia which became lethal in 3 months. The necrospy revealed a tumoral nodule in the left medulla oblongata and pons with diffuse subarachnoidal extension from the cranial nerves to the cauda equine roots. Histologically the tumor appeared to be polymorph with numerous rhabdomyoblasts which had a clear cross striation and which were sometimes less differentiated without any neuronal or glial elements. Perivascular tumoral cells and blood vessels were closely linked, the Virchow-Robin spaces were clearly involved. The electron microscopic study confirmed that the less differentiated cells were of a rhabdomyoblastic nature. A review of the litterature indicates that these malignant neoplasias are highly exceptional, and can be classified within the group of primary tumors of the neuraxis with muscular elements. The histogenetic origin of these tumors appears to be the ectomesenchyme of neural crests.

摘要

本文描述了一名8岁女孩患脑干原发性横纹肌肉瘤的病例。临床资料显示,该患儿起初出现右侧偏瘫,随后左侧第六脑神经完全麻痹,继而发展为截瘫,3个月后死亡。尸检发现左延髓和脑桥有一个肿瘤结节,肿瘤呈蛛网膜下腔弥漫性扩展,累及从脑神经到马尾神经根的区域。组织学上,肿瘤表现为多形性,有许多横纹肌母细胞,横纹清晰,有时分化程度较低,且无任何神经或神经胶质成分。肿瘤细胞与血管周围紧密相连,Virchow-Robin间隙明显受累。电子显微镜研究证实,分化程度较低的细胞具有横纹肌母细胞的性质。文献回顾表明,这些恶性肿瘤极为罕见,可归类为具有肌肉成分的神经轴原发性肿瘤。这些肿瘤的组织发生起源似乎是神经嵴的外胚层间充质。

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