急性多发性肌炎合并L-G-L综合征临床罕见,我院於198(?)年10月同时收治六例患者,经九年随访,现报告如下。本组6例均为女性,年龄16～25岁,平均(?)岁。急性起病,病因不明。全部病例均有两下肢及臀部肌肉疼痛发麻,明显压痛;心慌、胸闷、多汗、无力;小便呈酱油样。4例恶心呕吐,周身浮肿。2例呼吸困难, Acute polymyositis with L-G-L syndrome is clinically rare, our hospital in 198 (?) October at the same time admitted six patients, after nine years of follow-up, the report is as follows. The group of 6 patients were female, aged 16 to 25 years, mean (?) Years old. Acute onset, the cause is unknown. All cases had two lower extremities and buttocks muscle aches and pains, tenderness; palpitation, chest tightness, sweating, weakness; urine showed soy sauce. 4 cases of nausea and vomiting, whole body edema. 2 cases of dyspnea,