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炎性肌病合并间质性肺病的诊疗进展

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摘要 炎性肌病(idiopathic inflammatory myopathies,IIM)是一组横纹肌的非化脓性炎症性肌病,它是以对称性肢带肌、颈肌及吞咽肌无力为特征,常可导致多脏器受累,如肺脏、心脏、胃肠道等受累,并可发生全身症状如发热、乏力、消瘦等。IIM不是均一性疾病,而是含有多种亚型,包括PM、DM、包涵体肌炎、坏死性肌炎、结缔组织病相关性肌炎及与其他因素(如感染、药物、内分泌代谢性疾病及恶性肿瘤等)相关的肌炎。在临床上,以PM和DM最为多见,而在DM中,除了典型的DM外,无肌病性皮肌炎(ADM)是其常见的临床亚型。
出处 《中华风湿病学杂志》 CAS CSCD 北大核心 2017年第2期139-142,共4页 Chinese Journal of Rheumatology
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