Oda K, Fukushima N, Shibasaki H, Ohnishi A
Department of Internal Medicine (Division of Neurology), Saga Medical School, Japan.
Ann Neurol. 1989 Feb;25(2):140-5. doi: 10.1002/ana.410250206.
A case of Isaacs' syndrome with Trousseau's phenomenon is reported. Myokymia, pseudomyotonia (difficulty relaxing after forceful contraction), and ischemia-induced carpal spasm (Trousseau's phenomenon) were not abolished by nerve block distal to the cuff or by intravenous infusion of calcium. Inhalation of oxygen suppressed the pseudomyotonia and Trousseau's phenomenon, but myokymia persisted. Phenytoin abolished all types of abnormal discharges. The morphological abnormality in biopsied short peroneal muscle consisted of intraterminal and ultraterminal sprouting. We postulate that the trigger zone for abnormal discharge in our case is in the distal segment of the intramuscular nerve axon, including the nerve terminal. Hypoxia-sensitive hyperexcitability of the axon membrane might be responsible for the generation of pseudomyotonia and Trousseau's phenomenon, although the mechanism underlying myokymia remains unknown.
报告了一例伴有特鲁索现象的艾萨克斯综合征病例。肌束震颤、假肌强直(强力收缩后难以放松)以及缺血诱导的腕部痉挛(特鲁索现象),在袖带远端进行神经阻滞或静脉输注钙剂后均未消除。吸氧可抑制假肌强直和特鲁索现象,但肌束震颤持续存在。苯妥英消除了所有类型的异常放电。活检的腓骨短肌形态学异常包括终末内和终末外芽生。我们推测,本例中异常放电的触发区位于肌内神经轴突的远端节段,包括神经末梢。轴突膜对缺氧敏感的过度兴奋性可能是假肌强直和特鲁索现象产生的原因,尽管肌束震颤的潜在机制尚不清楚。