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Syndrome in question: antisynthetase syndrome (anti-PL-7)
Esposito, Ana Cláudia Cavalcante; Gige, Tatiana Cristina; Miot, Hélio Amante.
  • Esposito, Ana Cláudia Cavalcante; Universidade Estadual Paulista "Júlio de Mesquita Filho". Botucatu. BR
  • Gige, Tatiana Cristina; Universidade Estadual Paulista "Júlio de Mesquita Filho". Botucatu. BR
  • Miot, Hélio Amante; Universidade Estadual Paulista "Júlio de Mesquita Filho". Botucatu. BR
An. bras. dermatol ; 91(5): 683-685, Sept.-Oct. 2016. tab, graf
Article in English | LILACS | ID: biblio-827769
ABSTRACT
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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Full text: Available Index: LILACS (Americas) Main subject: Myositis Type of study: Prognostic study Limits: Adult / Female / Humans Language: English Journal: An. bras. dermatol Journal subject: Dermatology Year: 2016 Type: Article Affiliation country: Brazil Institution/Affiliation country: Universidade Estadual Paulista "Júlio de Mesquita Filho"/BR

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Full text: Available Index: LILACS (Americas) Main subject: Myositis Type of study: Prognostic study Limits: Adult / Female / Humans Language: English Journal: An. bras. dermatol Journal subject: Dermatology Year: 2016 Type: Article Affiliation country: Brazil Institution/Affiliation country: Universidade Estadual Paulista "Júlio de Mesquita Filho"/BR