RESUMEN
ABSTRACT The anomalous origin of one pulmonary artery from the ascending aorta is a rare congenital heart disease, generally diagnosed based on the clinical information and on echocardiographic and computed tomography angiography findings. Here we report two neonates successfully treated with surgery early in life.
RESUMEN
Descreve-se o caso de um homem de 19 anos assintomático com fibroma de ventrículo esquerdo em acompanhamento por 15 anos, sem tratamento.(AU)
Here we describe a case of a 19-year-old asymptomatic man with a left ventricular fibroma on follow-up for 15 years with no treatment required.(AU)
Asunto(s)
Humanos , Masculino , Adulto , Fibroma/diagnóstico por imagen , Neoplasias Cardíacas/complicaciones , Ventrículos Cardíacos/anomalías , Miocardio/patología , Ecocardiografía/métodos , Espectroscopía de Resonancia Magnética/métodos , Radiografía Torácica/métodos , Tomografía Computarizada por Rayos X/métodos , Electrocardiografía Ambulatoria/métodos , Muerte Súbita CardíacaRESUMEN
Acute obstruction of superior vena cava anastomosis right after the Glenn procedure may lead to tragic consequences. We describe the case of a one-year-old child with tricuspid atresia and a previous Blalock-Taussig shunt procedure, who presented severe low cardiac output syndrome right after the Glenn procedure and died forty-four hours after the procedure. The autopsy showed obstruction of the superior vena cava anastomosis. Patients that present superior vena cava syndrome and low cardiac output right after the Glenn procedure should have the surgical anastomosis revised immediately.