Suppr超能文献

格林-巴利综合征的临床病理研究——15例日本尸检病例

[A clinicopathological study of the Guillain-Barré syndrome--fifteen Japanese postmortem cases].

作者信息

Sobue G

机构信息

Department of Neurology, Nagoya University School of Medicine, Japan.

出版信息

Rinsho Shinkeigaku. 1995 Dec;35(12):1362-4.

PMID:8752396
Abstract

The postmortem findings of the ventral roots and ventral horn cells of 15 Japanese cases of Guillain-Barré syndrome are reported. In 5 cases there was predominant axonal involvement with severe axon loss in the lumber ventral root. Eight cases showed predominantly segmental demyelination, and two cases were the intermediate form with both segmental and axonal changes. Macrophage invasion in the ventral roots predominantly occurred in the cases with axonal involvement. Large-sized motor neuron loss and reactive astrogliosis were also seen in the cases with axonal degeneration. These findings indicate that approximately 30% of Japanese autopsied cases were "axonal form", the incidence of which was higher than that reported in European and North American countries, but was lower than that in Chinese endemic acute motor axonal neuropathy.

摘要

报告了15例日本格林-巴利综合征患者的腹侧神经根和腹角细胞的尸检结果。5例主要为轴突受累,腰段腹侧神经根有严重的轴突丧失。8例主要表现为节段性脱髓鞘,2例为节段性和轴突性改变并存的中间型。巨噬细胞浸润主要发生在轴突受累的病例的腹侧神经根中。轴突变性的病例中也可见大型运动神经元丧失和反应性星形胶质细胞增生。这些结果表明,约30%的日本尸检病例为“轴突型”,其发生率高于欧美国家报道的发生率,但低于中国地方性急性运动轴索性神经病的发生率。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验