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特发性炎性肌病:治疗进展

Idiopathic inflammatory myopathies: a treatment update.

作者信息

Oddis Chester V

机构信息

Department of Medicine, Division of Rheumatology and Clinical Immunology, University of Pittsburgh School of Medicine, S703 Biomedical Science Tower, 3500 Terrace Street, Pittsburgh, PA 15261, USA.

出版信息

Curr Rheumatol Rep. 2003 Dec;5(6):431-6. doi: 10.1007/s11926-003-0053-1.

Abstract

Inflammatory myopathies encompass a variety of syndromes with protean manifestations. Although the mainstay of therapy continues to include corticosteroids, there are a multitude of agents available for treating patients with myositis. These include many different immunosuppressive agents alone or in combination with each other, as well as an increasing array of novel and exciting biologic agents targeting molecules implicated in the pathogenesis of inflammatory myopathy. The systemic manifestations of myositis, particularly pulmonary involvement, are especially challenging to treat and contribute significantly to the morbidity and mortality of patients with polymyositis and dermatomyositis. Rehabilitative measures are often overlooked in the treatment of myositis, but may significantly improve the functional outcome of patients with these disorders.

摘要

炎性肌病包含多种具有多样临床表现的综合征。尽管治疗的主要手段仍然包括使用皮质类固醇,但有多种药物可用于治疗肌炎患者。这些药物包括许多不同的免疫抑制剂,可单独使用或相互联合使用,此外还有越来越多针对与炎性肌病发病机制相关分子的新型且令人振奋的生物制剂。肌炎的全身表现,尤其是肺部受累,在治疗上极具挑战性,并且对多发性肌炎和皮肌炎患者的发病率和死亡率有显著影响。康复措施在肌炎治疗中常常被忽视,但可能会显著改善这些疾病患者的功能预后。

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