重症肌无力症(MG)是一种神经肌肉联结点的激动传递障碍的自身免疫性疾病。在小儿多发生于眼肌等部。本文作者对于抗胆碱酯酶药物和类固醇等长期治疗情况下,反复再发的病例并非罕见,本文使用了大剂量甲基强的松龙静脉注射的冲击疗法,现就其效果与以往应用的类固醇疗法进行了比较和探讨,现报告于下。 Myasthenia gravis (MG) is an autoimmune disorder of the neurotransmitter’s agitating delivery disorder. Occurred in children and other eye muscle in the Ministry. The authors of the anticholinesterase drugs and steroids and other long-term treatment of cases of repeated recurrence is not uncommon, this article uses a large dose of methylprednisolone pulse therapy, now its effect and the previous application Steroid therapy were compared and discussed, the report is now under.