Abstract
Antisynthetase syndrome is a rare autoimmune disease characterized by interstitial lung disease and/or inflammatory myositis, with positive antisynthetase antibodies (anti-Jo-1, anti-PL-7, anti-PL-12, ZO, OJ, anti-KE or KS). Other symptoms described include: non-erosive arthritis, fever, Raynaud’s phenomenon, and "mechanic’s hands." The first therapeutic option is corticotherapy, followed by other immunosuppressants. The prognosis of the disease is quite limited when compared to other inflammatory myopathies with negative antisynthetase antibodies.
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Esposito, A. C. C., Miot, H. A., & Gige, T. C. (2016). Syndrome in question: Antisynthetase syndrome (anti-PL-7). Anais Brasileiros de Dermatologia, 91(5), 679–681. https://doi.org/10.1590/abd1806-4841.20164449
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