Bunch T W, Tancredi R G, Lie J T
Chest. 1981 Jan;79(1):105-7. doi: 10.1378/chest.79.1.105.
Pulmonary hypertension is an uncommon but lethal complication of polymyositis. A 69-year-old woman is described who had a 20-month history of polymyositis and cardiac failure and in whom severe pulmonary hypertension was noted terminally when she was first seen at our clinic. She died within 24 hours of admission, and autopsy revealed severe plexogenic pulmonary vascular disease.
肺动脉高压是多发性肌炎一种罕见但致命的并发症。本文描述了一位69岁女性，她有20个月的多发性肌炎和心力衰竭病史，首次在我们诊所就诊时终末期出现严重肺动脉高压。她在入院后24小时内死亡，尸检显示严重的丛状肺血管疾病。
