Anomalous origin of both coronary arteries from the pulmonary artery associated with tetralogy of fallot and patent ductus arteriosus.

摘要

Anomalous origin of the coronary arteries constitutes a group of congenital anomalies that occurs in 1% to 2% of congenital malformations. The most common type is anomalous left coronary artery from the main pulmonary artery (MPA) (ALCAPA). Both the left and the right pulmonary arteries arising from the MPA (ABCPA) is extremely rare, with a few cases reported. We report a young infant with ABCPA associated with tetralogy of Fallot (TOF) and patent ductus arteriosus (PDA).