Esper J J, Nigro M A, Wishnow R, Barnett T, Perrotta A L, Richardson W
Oakland General Hospital, Madison Heights, Mich.
J Am Osteopath Assoc. 1992 Aug;92(8):1056-8.
The authors report a case of eosinophilia-myalgia syndrome with a progressive neuromyopathy. Progressive weakness, myalgia, and dermatitis developed in the patient described after chronic ingestion of high-dose L-tryptophan for insomnia. Laboratory, electrophysiologic, and muscle biopsy results support the diagnosis of an inflammatory myopathy consistent with that of eosinophilia-myalgia syndrome. The patient's weakness led to wheelchair dependency. A review of the literature regarding this disorder shows inconsistent results with steroid and other modes of therapy. After a course of high-dose steroids with long-term tapering and vigorous inpatient and outpatient rehabilitation, the patient was able to walk and function independently within 2 months.
作者报告了一例伴有进行性神经肌肉病的嗜酸性粒细胞增多性肌痛综合征。该患者在长期大剂量服用L-色氨酸治疗失眠后,出现进行性肌无力、肌痛和皮炎。实验室检查、电生理检查及肌肉活检结果支持诊断为与嗜酸性粒细胞增多性肌痛综合征相符的炎性肌病。患者的肌无力导致需依赖轮椅。对有关该疾病的文献综述显示,类固醇及其他治疗方式的结果并不一致。经过一个疗程的大剂量类固醇治疗,长期逐渐减量,并进行积极的住院和门诊康复治疗后,患者在2个月内能够独立行走并自理。