Your browser doesn't support javascript.
loading
Brief report: antisynthetase syndrome-associated myocarditis.
Sharma, Kavita; Orbai, Ana-Maria; Desai, Dipan; Cingolani, Oscar H; Halushka, Marc K; Christopher-Stine, Lisa; Mammen, Andrew L; Wu, Katherine C; Zakaria, Sammy.
Afiliación
  • Sharma K; Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland. Electronic address: ksharma8@jhmi.edu.
  • Orbai AM; Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Desai D; Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Cingolani OH; Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Halushka MK; Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Christopher-Stine L; Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Mammen AL; Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland; Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Wu KC; Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Zakaria S; Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
J Card Fail ; 20(12): 939-45, 2014 Dec.
Article en En | MEDLINE | ID: mdl-25084215
BACKGROUND: The antisynthetase (AS) syndrome is characterized by autoimmune myopathy, interstitial lung disease, cutaneous involvement, arthritis, fever, and antibody specificity. We describe 2 patients with AS syndrome who also developed myocarditis, depressed biventricular function, and congestive heart failure. METHODS AND RESULTS: Both patients were diagnosed with AS syndrome based on clinical manifestations, detection of serum AS antibodies, and myositis confirmation with the use of skeletal muscle magnetic resonance imaging and skeletal muscle biopsy. In addition, myocarditis resulting in heart failure was confirmed with the use of cardiac magnetic resonance imaging and from endomyocardial biopsy findings. After treatment for presumed AS syndrome-associated myocarditis, one patient recovered and the other patient died. CONCLUSIONS: AS syndrome is a rare entity with morbidity and mortality typically attributed to myositis and lung involvement. This is the first report of AS syndrome-associated myocarditis leading to congestive heart failure in 2 patients. Given the potentially fatal consequences, myocarditis should be considered in patients with AS syndrome presenting with heart failure.
Asunto(s)
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Insuficiencia Cardíaca / Miocarditis / Miositis Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: J Card Fail Asunto de la revista: CARDIOLOGIA Año: 2014 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Insuficiencia Cardíaca / Miocarditis / Miositis Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: J Card Fail Asunto de la revista: CARDIOLOGIA Año: 2014 Tipo del documento: Article