The origin of spontaneous discharges in acquired neuromyotonia.: A Macro EMG study

被引:27
作者
Arimura, K
Arimura, Y
Ng, A
Uehara, A
Nakae, M
Osame, M
Stålberg, E
机构
[1] Kagoshima Univ, Grad Sch Med & Dent Sci, Dept Neurol & Geriatr, Kagoshima 890, Japan
[2] Univ Uppsala Hosp, Ctr Clin Neurosci, Dept Clin Neurophysiol, S-75185 Uppsala, Sweden
关键词
neuromyotonia; Isaacs' syndrome; Macro EMG; spontaneous discharges; VGKC antibodies;
D O I
10.1016/j.clinph.2005.03.023
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To study the generator sites of spontaneous discharges in patients with immune-mediated neuromyotonia. Methods: Macro EMGs triggered by both spontaneously and voluntarily activated single action potentials were recorded and the mean peak-to-peak amplitude and area of the macro motor unit potentials were compared in two patients with typical acquired neuromyotonia,having positive antibodies against voltage-gated potassium channels. Results: Mean peak-to-peak amplitude and area of Macro EMG motor unit potentials (macro MUPs) triggered by spontaneous discharges were significantly smaller than those triggered by voluntary activation in both patients. However, a few macro MUPs triggered by spontaneous discharges resembled those triggered by voluntary activation. Conclusions: Spontaneous discharges in two patients with immune-mediated neuromyotonia seem to be mostly generated at sites distal to the terminal axon branching points. Significance: This finding may provide a new insight in the understanding of spontaneous discharges in immune-mediated neuromyotonia. (c) 2005 International Federation of Clinical Neurophysiology. Published by Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:1835 / 1839
页数:5
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