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间质性肺纤维化在皮肌炎或多肌炎比在硬皮病及类风湿性关节炎少见。近10年来我院收治的皮肌炎和多肌炎可供分析的病历资料共18例,其中5例并发间质性肺纤维化(IPF)。现就此5例的临床情况(包括1例的尸检结果)报告如下。临床资料1.病例选择:皮肌炎16例和多肌炎2例全部符合1975年Bohan提出的诊断标准。其中男性5例(均为皮肌炎),女性13例(2例为多肌炎)。发病年龄11～68岁,平均35岁。
Interstitial pulmonary fibrosis is less common in dermatomyositis or polymyositis than in scleroderma and rheumatoid arthritis. In the past 10 years, 18 cases of dermatomyositis and polymyositis were analyzed in our hospital, of which 5 cases were complicated with interstitial pulmonary fibrosis (IPF). Now on the clinical situation of 5 cases (including 1 cases of autopsy results) reported as follows. Clinical data 1. Case selection: 16 cases of dermatomyositis and polymyositis in 2 cases all meet the diagnostic criteria proposed by Bohan in 1975. There were 5 males (all dermatomyositis) and 13 females (2 polymyositis). The onset of age 11 to 68 years old, with an average of 35 years old.