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Syndrome in question: antisynthetase syndrome (anti-PL-7)

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...

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Autores principales: Esposito, Ana Cláudia Cavalcante, Gige, Tatiana Cristina, Miot, Hélio Amante
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Dermatologia 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5087238/
https://www.ncbi.nlm.nih.gov/pubmed/27828653
http://dx.doi.org/10.1590/abd1806-4841.20164449
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author Esposito, Ana Cláudia Cavalcante
Gige, Tatiana Cristina
Miot, Hélio Amante
author_facet Esposito, Ana Cláudia Cavalcante
Gige, Tatiana Cristina
Miot, Hélio Amante
author_sort Esposito, Ana Cláudia Cavalcante
collection PubMed
description 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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spelling pubmed-50872382016-11-01 Syndrome in question: antisynthetase syndrome (anti-PL-7) Esposito, Ana Cláudia Cavalcante Gige, Tatiana Cristina Miot, Hélio Amante An Bras Dermatol Syndrome in Question 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. Sociedade Brasileira de Dermatologia 2016 /pmc/articles/PMC5087238/ /pubmed/27828653 http://dx.doi.org/10.1590/abd1806-4841.20164449 Text en ©2016 by Anais Brasileiros de Dermatologia http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License which permits unrestricted non-commercial use, distribution, and reproduction in any medium provided the original work is properly cited.
spellingShingle Syndrome in Question
Esposito, Ana Cláudia Cavalcante
Gige, Tatiana Cristina
Miot, Hélio Amante
Syndrome in question: antisynthetase syndrome (anti-PL-7)
title Syndrome in question: antisynthetase syndrome (anti-PL-7)
title_full Syndrome in question: antisynthetase syndrome (anti-PL-7)
title_fullStr Syndrome in question: antisynthetase syndrome (anti-PL-7)
title_full_unstemmed Syndrome in question: antisynthetase syndrome (anti-PL-7)
title_short Syndrome in question: antisynthetase syndrome (anti-PL-7)
title_sort syndrome in question: antisynthetase syndrome (anti-pl-7)
topic Syndrome in Question
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5087238/
https://www.ncbi.nlm.nih.gov/pubmed/27828653
http://dx.doi.org/10.1590/abd1806-4841.20164449
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