• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

以近端受累为主的脱髓鞘性多发性神经病。

Demyelinating polyneuropathy with preferentially-proximal involvement.

作者信息

Asahina M, Kuwabara S, Nakajima M, Yamada T

机构信息

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

出版信息

Clin Neurol Neurosurg. 1998 Mar;100(1):53-5. doi: 10.1016/s0303-8467(97)00121-2.

DOI:10.1016/s0303-8467(97)00121-2
PMID:9637207
Abstract

A 47-year-old man showed progressive, symmetrical weakness in the limbs for 6 months. There was muscle atrophy, fasciculations, and acute denervation without motor conduction abnormalities below the elbows or knees, and motor neuron disease had once been suspected. However, compound muscle action potentials (CMAPs) after proximal stimulation showed an amplitude reduction between axilla and Erb's point for the median and ulnar nerves on both sides. His weakness as well as the amplitude reduction improved after administration of prednisolone. Demyelinative conduction abnormalities can be limited to the proximal segments for at least several months in a conduction equivalent to chronic inflammatory demyelinating polyneuropathy (CIDP).

摘要

一名47岁男性出现四肢进行性对称性无力6个月。存在肌肉萎缩、肌束震颤及急性去神经改变,肘或膝以下无运动传导异常,曾怀疑患有运动神经元病。然而,双侧正中神经和尺神经近端刺激后的复合肌肉动作电位(CMAPs)显示腋窝与Erb点之间波幅降低。给予泼尼松龙后,其无力症状及波幅降低情况有所改善。脱髓鞘性传导异常在相当于慢性炎症性脱髓鞘性多发性神经病(CIDP)的传导中,可局限于近端节段至少数月。

相似文献

1
Demyelinating polyneuropathy with preferentially-proximal involvement.以近端受累为主的脱髓鞘性多发性神经病。
Clin Neurol Neurosurg. 1998 Mar;100(1):53-5. doi: 10.1016/s0303-8467(97)00121-2.
2
[Chronic inflammatory demyelinating polyneuropathy--an electrophysiological and histological study of the ulnar nerve from a case with intractable persistent conduction block].
Rinsho Shinkeigaku. 1992 Jun;32(6):616-20.
3
Motor variant of chronic inflammatory demyelinating polyneuropathy in a child.一名儿童慢性炎症性脱髓鞘性多发性神经病的运动变异型
Pediatr Neurol. 2008 Jun;38(6):426-9. doi: 10.1016/j.pediatrneurol.2008.02.008.
4
Dispersion of compound muscle action potential in hereditary neuropathies and chronic inflammatory demyelinating polyneuropathy.遗传性神经病和慢性炎症性脱髓鞘性多发性神经病中复合肌肉动作电位的离散度
Muscle Nerve. 2006 Oct;34(4):417-22. doi: 10.1002/mus.20600.
5
[Multifocal-motor neuropathy and motor neuropathy with multifocal conduction block (Lewis-Sumner syndrome)].[多灶性运动神经病与多灶性传导阻滞性运动神经病(刘易斯 - 萨姆纳综合征)]
Wien Klin Wochenschr. 1995;107(10):301-8.
6
[Nerve conduction abnormalities in chronic inflammatory demyelinating polyneuropathy (CIDP)].慢性炎症性脱髓鞘性多发性神经病(CIDP)中的神经传导异常
Rinsho Shinkeigaku. 1991 Dec;31(12):1333-6.
7
[Chronic inflammatory demyelinating polyneuropathy in childhood--a case with markedly hypertrophic nerves and pes cavus].儿童慢性炎症性脱髓鞘性多发性神经病——1例伴有明显肥大神经和高弓足的病例
Rinsho Shinkeigaku. 1993 Jan;33(1):36-9.
8
Asymmetrical polyneuropathy with a stepwise progressive course and well-demarcated areas of demyelination.不对称性多发性神经病,病程呈阶梯式进展,脱髓鞘区域界限清晰。
Muscle Nerve. 1999 Aug;22(8):1139-45. doi: 10.1002/(sici)1097-4598(199908)22:8<1139::aid-mus22>3.0.co;2-x.
9
Upper limb predominant, multifocal chronic inflammatory demyelinating polyneuropathy.上肢为主型多灶性慢性炎症性脱髓鞘性多发性神经病
Muscle Nerve. 1999 Jun;22(6):758-65. doi: 10.1002/(sici)1097-4598(199906)22:6<758::aid-mus13>3.0.co;2-n.
10
[A case of chronic and progressive distal symmetric type CIDP with subacute exacerbation: focus on clinical pattern of CIDP].[1例伴有亚急性加重的慢性进行性远端对称型慢性炎性脱髓鞘性多发性神经病:聚焦慢性炎性脱髓鞘性多发性神经病的临床模式]
Rinsho Shinkeigaku. 2011 Feb;51(2):141-4. doi: 10.5692/clinicalneurol.51.141.

引用本文的文献

1
A case of steroid-responsive MADSAM with late appearance of a partial conduction block in the forearm.一例对类固醇有反应的多灶性获得性脱髓鞘性感觉和运动神经病,前臂出现迟发性部分传导阻滞。
J Neurol. 2014 Apr;261(4):825-7. doi: 10.1007/s00415-014-7271-5. Epub 2014 Feb 26.