Treatment of Libman-Sacks endocarditis by combination of warfarin and immunosuppressive therapy

Antiphospholipid syndrome (APS) is a clinical disorder that creates an increased risk of arterial or venous thrombotic events or pregnancy-associated complications and includes the presence of autoantibodies against negatively charged phospholipids. This syndrome is often associated with systemic au...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Mehmet Rasih Sonsöz (Autor), Rukiye Dilara Tekin (Autor), Ahmet Gül (Autor), Zehra Buğra (Autor), Dursun Atılgan (Autor)
Formato: Libro
Publicado: KARE Publishing, 2019-12-01T00:00:00Z.
Materias:
Acceso en línea:Connect to this object online.
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
Descripción
Sumario:Antiphospholipid syndrome (APS) is a clinical disorder that creates an increased risk of arterial or venous thrombotic events or pregnancy-associated complications and includes the presence of autoantibodies against negatively charged phospholipids. This syndrome is often associated with systemic autoimmune diseases, such as systemic lupus erythematosus (SLE). Libman-Sacks endocarditis is a form of non-bacterial thrombotic endocarditis and is infrequently seen in APS. There are few data documenting the echocardiographic response of APS valve disease to medical treatment. This is an unusual case of a young female patient with SLE and APS who had chorea and non-bacterial thrombotic aortic valve endocarditis. Echocardiography revealed that the vegetation had receded after a combination of warfarin and immunosuppressive therapy.
Notas:1016-5169
10.5543/tkda.2019.29213