Morović-Vergles Jadranka, Mitrović Josko
Zavod za klinicku imunologiju i reumatologiju, Klinicka za unutarnje bolesti, Klinicka bolnica Dubrava, Avenija G. Suska 6, 10000 Zagreb.
Reumatizam. 2012;59(2):23-6.
The idiopathic inflammatory myopathies, collectively called myositis, are a heterogeneous group of diseases of which polymyositis and dermatomyositis are the best known. These heterogeneous group of chronic disordes sharing the clinical symptom of muscle weakness and, in typical cases, inflammatory cell infiltrates in muscle tissue. There are four major types of idiopathic inflammatory myopathies: dermatomyositis, polymyositis, inclusion body myositis and immune-mediated necrotizing myopathies (autoimmune necrotizing myopathies). Clinical and histopatological distinctions between these conditions suggest that different pathogenic processes underline each of the inflammatory myopathies.
特发性炎性肌病,统称为肌炎,是一组异质性疾病,其中多发性肌炎和皮肌炎最为人所知。这些异质性的慢性疾病具有肌肉无力的临床症状,在典型病例中,肌肉组织存在炎性细胞浸润。特发性炎性肌病主要有四种类型:皮肌炎、多发性肌炎、包涵体肌炎和免疫介导的坏死性肌病(自身免疫性坏死性肌病)。这些疾病在临床和组织病理学上的差异表明,不同的致病过程是每种炎性肌病的基础。