无肌病性皮肌炎八例临床特征分析  

Clinical features of amyopathic dermatomyositis

作　　者：周晓洁[1] 袁双龙[1] 周蕾[1] 巩路[1] 

机构地区：[1]天津医科大学总医院感染免疫科,300052

出　　处：《中华全科医师杂志》2010年第3期206-207,共2页Chinese Journal of General Practitioners

摘　　要：收集近4年皮肌炎患者61例，其中8例无肌病性皮肌炎患者（观察组），53例典型皮肌炎患者（对照组），分析两组患者的临床特点。结果示观察组肺间质病变、关节痛、发热者分别为4例、3例、3例；对照组肺间质病变、关节痛、发热、肿瘤者分别为21例（40％）、18例（34％）、17例（32％）和6例（11％）。无肌病性皮肌炎者肺间质病变的发生率较高，虽没有明显肌病表现，但可累及内脏。The clinical features of 8 cases with amyopathic dermatomyositis （ADM） were retrospectively compared with those of 53 cases with typical dermatomyositis （DM）. Incidence of interstitial lung disease, joint pain, fever, concurrent cancer were 4/8, 3/8, 3/8 and 0 in ADM group and those were 40% , 34% , 32% and 11% in DM group respectively. The prevalence of interstitial lung disease in ADM group was significantly higher than that in DM group, which indicates that ADM patient should be properly treated.

关 键 词：皮肌炎 肺疾病 间质性 

分 类 号：R593.26[医药卫生—内科学] R563[医药卫生—临床医学]