Pohlmann-Eden B, Berlit P, Janta B
Neurologische Klinik, Klinikum Mannheim der Universität Heidelberg.
Nervenarzt. 1988 May;59(5):304-8.
The case of a patient with spontaneous painful muscular activity is described. We diagnosed the muscular pain fasciculation syndrome. Biopsy of the sural nerve and electrophysiological examination provided evidence of the neurogenic nature of the disturbance showing a remarkable axonal degeneration. In addition, when immunohistochemical studies were performed, the detection of immunoglobulins and complement components suggested an immunological process in the etiology of the disease. The patient made a good response to carbamazepine therapy. This effect is found in various syndromes of abnormal continuous muscle activity. Clinical, neurophysiological and morphological features of this case are discussed in relation of pathogenesis, possible drug effects and related diseases.
本文描述了一例患有自发性疼痛性肌肉活动的患者。我们诊断为肌肉疼痛性肌束震颤综合征。腓肠神经活检和电生理检查提供了神经源性病变的证据,显示出明显的轴索变性。此外,进行免疫组化研究时,免疫球蛋白和补体成分的检测提示该病病因中存在免疫过程。患者对卡马西平治疗反应良好。这种效应在各种异常持续性肌肉活动综合征中均有发现。结合发病机制、可能的药物作用及相关疾病,讨论了该病例的临床、神经生理和形态学特征。