Asymptomatic ALCAPA with Preserved Myocardial Function in a 3-Year-Old Child
C Leclercq1, F Kaladji2, J P Vallée3
1Pediatric Cardiology Unit, University Hospital of Geneva, Geneva, Switzerland. Charlotte.Leclercq@hug.ch.
None:
Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital anomaly. Its clinical course is typically severe in infancy, leading to left ventricular ischemia, cardiogenic shock, and high mortality without surgical intervention.We describe a rare case of a 3-year-old girl diagnosed with ALCAPA, showing extensive right-to-left collaterals, preserved left ventricular function, and minimal myocardial injury.
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