RESUMEN

Anomalous left coronary artery from the pulmonary artery (ALCAPA) is an uncommon life-threatening congenital heart defect that occurs mostly as an isolated lesion. It is very rarely associated with other cardiac abnormalities. In this report, we present a case of an infant who successfully underwent complete surgical repair of a rare triad of congenital heart defects, including ALCAPA, ventricular septal defect (VSD), and double aortic arch (DAA). To the best of our knowledge, this is only the second case of ALCAPA diagnosis associated with VSD and DAA that has been described in the literature.

Asunto(s)

Aorta Torácica , Defectos del Tabique Interventricular , Arteria Pulmonar , Humanos , Defectos del Tabique Interventricular/cirugía , Defectos del Tabique Interventricular/complicaciones , Defectos del Tabique Interventricular/diagnóstico por imagen , Aorta Torácica/anomalías , Aorta Torácica/cirugía , Aorta Torácica/diagnóstico por imagen , Arteria Pulmonar/anomalías , Arteria Pulmonar/cirugía , Arteria Pulmonar/diagnóstico por imagen , Anomalías Múltiples/cirugía , Lactante , Masculino , Arteria Coronaria Izquierda Anómala/cirugía , Procedimientos Quirúrgicos Cardíacos/métodos , Recién Nacido , Femenino , Ecocardiografía