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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Dermatologia
2016
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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. |
format | Online Article Text |
id | pubmed-5087238 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Sociedade Brasileira de Dermatologia |
record_format | MEDLINE/PubMed |
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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