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A Case of Anti-SAE1 Dermatomyositis

de Vries, Max ; Schreurs, Marco W. J. ; Ahsmann, Els J. M. ; Spee-Dropkova, Marcela ; Karim, Faiz Litzman, Jiri ; Jiri Litzman

Case reports in immunology, 2022, Vol.2022, p.9000608-4 [Periódico revisado por pares]

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Título:
A Case of Anti-SAE1 Dermatomyositis
Autor: de Vries, Max ; Schreurs, Marco W. J. ; Ahsmann, Els J. M. ; Spee-Dropkova, Marcela ; Karim, Faiz
Litzman, Jiri ; Jiri Litzman
Assuntos: Antibodies ; Arthralgia ; Biopsy ; Cancer ; Carbon monoxide ; Case Report ; Case reports ; Dermatomyositis ; Dysphagia ; Enzymes ; Exanthema ; Glucocorticoids ; Heart attacks ; Hypertension ; Immunology ; Laboratories ; Lung diseases ; Lupus ; Patients ; Pneumonia ; Remission ; Respiratory function ; Rheumatic diseases ; Rheumatology ; Scleroderma ; Thrombocytopenia ; White people
É parte de: Case reports in immunology, 2022, Vol.2022, p.9000608-4
Notas: Academic Editor: Jiri Litzman
Descrição: 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.
Editor: Egypt: Hindawi
Idioma: Inglês

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