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Rev. bras. cardiol. (Impr.) ; 27(5): 374-377, set.-out. 2014. ilus
Article in Portuguese | LILACS | ID: lil-742410

ABSTRACT

Miocardiopatia periparto é uma síndrome rara, de etiologia ainda desconhecida, caracterizada por disfunção ventricular esquerda nova, no último mês da gestação ou nos primeiros seis meses pós-parto. Os fatores de risco incluem multíparas, gestação gemelar, etnia negra e idade materna >30 anos. Relata-se o caso de miocardiopatia periparto em adolescente de 13 anos, negra, primípara de feto único, com cardiopatiasassociadas (valva aórtica bicúspide e síndrome deWolff-Parkinson-White) que evoluiu com complicações tromboembólicas e desfecho desfavorável.


Peripartum cardiomyopathy is a rare syndrome of unknown etiology, characterized by new left ventricular dysfunction in the last month of pregnancy or during the first six months postpartum. Risk factors include multiparous, twin pregnancy, black ethnicity and maternal age above 30 years. This report describes a case of peripartum cardiomyopathy in black female (13 years old), primiparous, single fetus, associated with cardipatias (bicuspid aortic valve and Wolff- Parkinson-White syndrome) who developed thromboembolic complications with an unfavorable outcome.


Subject(s)
Humans , Female , Adolescent , Cardiomyopathies/etiology , Aortic Valve Insufficiency/complications , Peripartum Period , Wolff-Parkinson-White Syndrome/physiopathology , Echocardiography/methods , Electrocardiography/methods , Risk Factors , Prognosis , Thromboembolism/complications
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