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A case of myocardial infarction with antiphospholipid syndrome / 대한내과학회지
Korean Journal of Medicine ; : 108-111, 2008.
Article em Ko | WPRIM | ID: wpr-164617
Biblioteca responsável: WPRO
ABSTRACT
Antiphospholipid syndrome is a multi-system disorder characterized by arterial or venous thromboses and antiphospholipid antibodies, such as lupus anticoagulant or anticardiolipin antibodies. Most common clinical manifestations are recurrent pregnancy losses and deep vein thromboses. Cardiac manifestations in antiphospholipid syndrome include valve abnormalities, occlusive arterial disease, intracardiac emboli, and ventricular dysfunction. Acute myocardial infarction is a rare manifestation of the primary antiphospholipid syndrome. We have experienced a case of myocardial infarction with antiphospholipid syndrome. A 35-year-old man with no cardiovascular risk factors, other than smoking, presented with chest pain. He was diagnosed with an acute myocardial infarction. Our evaluation for coagulapathy revealed elevated lupus anticoagulant antibody. The antiphospholipid syndrome should be considered early in the differential diagnosis as an important cause of unexplained thrombosis in young patients.
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Texto completo: 1 Índice: WPRIM Assunto principal: Fumaça / Trombose / Dor no Peito / Fumar / Fatores de Risco / Inibidor de Coagulação do Lúpus / Síndrome Antifosfolipídica / Anticorpos Antifosfolipídeos / Anticorpos Anticardiolipina / Disfunção Ventricular Tipo de estudo: Diagnostic_studies / Etiology_studies / Risk_factors_studies Limite: Adult / Humans / Pregnancy Idioma: Ko Revista: Korean Journal of Medicine Ano de publicação: 2008 Tipo de documento: Article
Texto completo: 1 Índice: WPRIM Assunto principal: Fumaça / Trombose / Dor no Peito / Fumar / Fatores de Risco / Inibidor de Coagulação do Lúpus / Síndrome Antifosfolipídica / Anticorpos Antifosfolipídeos / Anticorpos Anticardiolipina / Disfunção Ventricular Tipo de estudo: Diagnostic_studies / Etiology_studies / Risk_factors_studies Limite: Adult / Humans / Pregnancy Idioma: Ko Revista: Korean Journal of Medicine Ano de publicação: 2008 Tipo de documento: Article