Antiphospholipid syndrome and cardiac tumors

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We present the case of a 31-year-old female patient with a history of bilateral staghorn lithiasis, who started the disease one month before admission with thrombocytopenia and autoimmune hemolytic anemia. She was diagnosed with Evans Syndrome, initially she had negative autoimmunity markers, finall...

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Detalles Bibliográficos
Autores: León-Jiménez, Franco E., Juarez-Lloclla, Jorge P.
Formato: artículo
Fecha de Publicación:2023
Institución:Universidad Nacional Mayor de San Marcos
Repositorio:Revistas - Universidad Nacional Mayor de San Marcos
Lenguaje:español
OAI Identifier:oai:ojs.csi.unmsm:article/24174
Enlace del recurso:https://revistasinvestigacion.unmsm.edu.pe/index.php/anales/article/view/24174
Nivel de acceso:acceso abierto
Materia:Antiphospholipid Syndrome
Thrombosis
Death, Sudden
Síndrome Antifosfolípido
Trombosis
Muerte Súbita
Descripción
Sumario:We present the case of a 31-year-old female patient with a history of bilateral staghorn lithiasis, who started the disease one month before admission with thrombocytopenia and autoimmune hemolytic anemia. She was diagnosed with Evans Syndrome, initially she had negative autoimmunity markers, finally presented progressive dyspnea and 4 intracardiac masses were found in the right atrium and positive markers for antiphospholipid syndrome. Despite anticoagulation and preparation for cardiac surgery, she presented sudden death.
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