结节病中的结节传导阻滞和结节间传导阻滞。

Q3 Medicine
Shin J Oh
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引用次数: 0

摘要

目的:2015 年,"结节病 "这一新术语被引入,以代表一组因 Ranvier 节点和结节旁区域自身抗体而导致的神经病变。本综述旨在通过新引入的术语突出急性和慢性结节病的电生理学特征:"结节传导阻滞(CB);无时间弥散或神经传导速度缓慢的 CB",并引入了一个新术语:"方法:通过在 PubMed 上的搜索,确定了 23 例急性(神经病变 4 周)结节病病例。另外两个必要的纳入标准是结节抗体检测呈阳性和有或无图的详细神经传导数据。我们对所有现有数据进行了分析,以确定这些病例是结节性还是节间 CB:结果:在 23 例急性结节病病例中,11 例为结节性 CB,9 例为节间 CB,3 例为混合 CB。因此,在 61% 的急性结节病病例中观察到结节 CB,在 52% 的急性结节病病例中观察到节间 CB。在 12 例慢性结节病病例中,所有 12 例均为节间 CB:结节CB是急性结节病的神经传导特征,但节间CB并不能排除急性结节病。节间 CB 是慢性结节病的神经传导特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nodal Conduction Block and Internodal Conduction Block in Nodopathy.

Objectives: In 2015, a new term "nodopathy" was introduced to represent a group of neuropathy because of autoantibodies at the node of Ranvier and paranodal area. This review was conducted to highlight the electrophysiologic characteristics of acute and chronic nodopathies by the newly introduced term: "nodal conduction block (CB); CB without temporal dispersion or slow nerve conduction velocity" and by introducing a new term: "internodal CB; CB with temporal dispersion or/and slow nerve conduction velocity".

Methods: Through PubMed searches, 23 cases of acute (<4 weeks of neuropathy) nodopathy and 12 cases of chronic (>4 weeks of neuropathy) nodopathy are identified. Two other required inclusion criteria are positive nodal antibody test and detailed nerve conduction data with or without figure. All existing data were analyzed to see whether these cases had nodal or internodal CB.

Results: Among 23 cases of acute nodopathy, 11 had nodal CB, 9 internodal CB, and 3 mixed CB. Thus, nodal CB was observed in 61% of acute nodopathy cases and internodal CB in 52% of acute nodopathy cases. Among 12 cases of chronic nodopathy, all 12 had internodal CB.

Conclusions: Nodal CB is the nerve conduction characteristic of acute nodopathy, but internodal CB does not rule out acute nodopathy. Internodal CB is the nerve conduction characteristic of chronic nodopathy.

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来源期刊
CiteScore
1.60
自引率
0.00%
发文量
64
期刊介绍: Journal of Clinical Neuromuscular Disease provides original articles of interest to physicians who treat patients with neuromuscular diseases, including disorders of the motor neuron, peripheral nerves, neuromuscular junction, muscle, and autonomic nervous system. Each issue highlights the most advanced and successful approaches to diagnosis, functional assessment, surgical intervention, pharmacologic treatment, rehabilitation, and more.
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