Pazanin Leo
Klinicki zavod za patologiju Ljudevit Jurak, Klinicki bolnicki centar, Sestre milosrdnice, Vinogradska 29, 10000 Zagreb.
Reumatizam. 2012;59(2):35-8.
The idiopathic inflammatory myopathies represent a group ofimmunologically mediated diseases characterized by inflammation of skeletal muscle potentially leading to irreversible damage. On the basis of clinical, histological and immunological features dermatomyositis, polymyositis and sporadic inclusion-body myositis are recognized as separate entities. A definitive diagnosis of idiopathic inflammatory myopathies requires detailed histological, histochemical, immunohistochemical and electron-microscopic analysis of adequate muscle biopsy sample. However, in spite of thorough morphological analysis distinction of these disorders is not always straightforward and a close clinicopathological correlation is often essential to reach a correct diagnosis. Detailed morphological features ofidiopathic inflammatory myopathies and their relationship to pathogenesis is outlined.
特发性炎性肌病是一组免疫介导的疾病,其特征是骨骼肌炎症,可能导致不可逆损伤。根据临床、组织学和免疫学特征,皮肌炎、多发性肌炎和散发性包涵体肌炎被认为是不同的疾病实体。特发性炎性肌病的明确诊断需要对足够的肌肉活检样本进行详细的组织学、组织化学、免疫组织化学和电子显微镜分析。然而,尽管进行了全面的形态学分析,这些疾病的区分并不总是一目了然,紧密的临床病理相关性对于做出正确诊断往往至关重要。本文概述了特发性炎性肌病的详细形态学特征及其与发病机制的关系。