多发性肌炎
肌炎
皮肌炎
医学
抗合成酶综合征
肌病
炎性肌病
皮肤病科
重症监护医学
恶化
免疫学
内科学
自身抗体
抗体
作者
Nicolò Pipitone,Carlo Salvarani
标识
DOI:10.1097/bor.0000000000000745
摘要
Purpose of review Myositis, or idiopathic inflammatory myopathy, is an overarching concept that includes dermatomyositis, polymyositis, immune-mediated necrotizing myopathy and the antisynthetase syndrome. Glucocorticoids are still considered the mainstay of treatment of myositis but some patients require add-on immunosuppressive therapy because of insufficient response to glucocorticoids, relapses when glucocorticoids are tapered, or because they incur glucocorticoid-related side effects. Recent findings The goal of this article was to review (PubMed search from January 2019 through June 2020) the efficacy and safety of standard and novel agents used in adult dermatomyositis, polymyositis, immune-mediated necrotizing myopathy and the antisynthetase syndrome. Summary Established therapies beyond glucocorticoids continue to have a major role in managing patients with myositis. In addition, novel agents are being tried for refractory manifestations of myositis.
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