A Case of Anti-SAE1 Dermatomyositis

INTRODUCTION: Anti-SAE1 antibodies have a low prevalence in dermatomyositis patients. Case Description. A 61-year-old woman presented with progressive shortness of breath, arthralgia, heliotrope rash, Gottron's papules, and erythematous rash. She had an interstitial lung disease (ILD) with a si...

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Detalles Bibliográficos
Autores principales: de Vries, Max, Schreurs, Marco W. J., Ahsmann, Els J. M., Spee-Dropkova, Marcela, Karim, Faiz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8916888/
https://www.ncbi.nlm.nih.gov/pubmed/35280599
http://dx.doi.org/10.1155/2022/9000608
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author de Vries, Max
Schreurs, Marco W. J.
Ahsmann, Els J. M.
Spee-Dropkova, Marcela
Karim, Faiz
author_facet de Vries, Max
Schreurs, Marco W. J.
Ahsmann, Els J. M.
Spee-Dropkova, Marcela
Karim, Faiz
author_sort de Vries, Max
collection PubMed
description INTRODUCTION: Anti-SAE1 antibodies have a low prevalence in dermatomyositis patients. Case Description. A 61-year-old woman presented with progressive shortness of breath, arthralgia, heliotrope rash, Gottron's papules, and erythematous rash. She had an interstitial lung disease (ILD) with a significant decrease in lung function. There was no muscle involvement. Immunological laboratory test results showed strongly positive anti-SAE1 antibodies. Glucocorticoid treatment resulted in remission of dermatomyositis. CONCLUSION: Anti-SAE antibodies in dermatomyositis patients are closely linked to unique clinical features.
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spelling pubmed-89168882022-03-12 A Case of Anti-SAE1 Dermatomyositis de Vries, Max Schreurs, Marco W. J. Ahsmann, Els J. M. Spee-Dropkova, Marcela Karim, Faiz Case Reports Immunol Case Report INTRODUCTION: Anti-SAE1 antibodies have a low prevalence in dermatomyositis patients. Case Description. A 61-year-old woman presented with progressive shortness of breath, arthralgia, heliotrope rash, Gottron's papules, and erythematous rash. She had an interstitial lung disease (ILD) with a significant decrease in lung function. There was no muscle involvement. Immunological laboratory test results showed strongly positive anti-SAE1 antibodies. Glucocorticoid treatment resulted in remission of dermatomyositis. CONCLUSION: Anti-SAE antibodies in dermatomyositis patients are closely linked to unique clinical features. Hindawi 2022-03-04 /pmc/articles/PMC8916888/ /pubmed/35280599 http://dx.doi.org/10.1155/2022/9000608 Text en Copyright © 2022 Max de Vries et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
de Vries, Max
Schreurs, Marco W. J.
Ahsmann, Els J. M.
Spee-Dropkova, Marcela
Karim, Faiz
A Case of Anti-SAE1 Dermatomyositis
title A Case of Anti-SAE1 Dermatomyositis
title_full A Case of Anti-SAE1 Dermatomyositis
title_fullStr A Case of Anti-SAE1 Dermatomyositis
title_full_unstemmed A Case of Anti-SAE1 Dermatomyositis
title_short A Case of Anti-SAE1 Dermatomyositis
title_sort case of anti-sae1 dermatomyositis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8916888/
https://www.ncbi.nlm.nih.gov/pubmed/35280599
http://dx.doi.org/10.1155/2022/9000608
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