Anomalous left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital cardiac malformation accounting for approximately 1 in 300,000 live births. 1 The first reported child with ALCAPA was described by Russian pathologist Alexei Ivanovich Abrikosov in 1911, when he described postmortem ''a left ventricular aneurysm with anomalous origin of the left coronary artery from pulmonary artery in a 5-month old child.'' 2 A comprehensive clinical description was given in 1933 by American physicians Edward Bland, Paul Dudley White, and Joseph Garland. 3 Thus, a typical clinical presentation is often referred to today as Bland-White-Garland syndrome.