ALCAPA Diagnosed in an Elderly Patient
Thomas C Pointer1, John F Keaney1, Samuel W Reinhardt2
1Department of Pediatrics, Yale School of Medicine, New Haven, Connecticut, USA; Yale-New Haven Hospital, New Haven, Connecticut, USA.
Anomalous left coronary artery origin arising from the pulmonary artery (ALCAPA) is rare and usually fatal in infancy. This case shows a 66-year-old woman with undiagnosed ALCAPA who remained asymptomatic with medical management alone.
Area of Science:
- Cardiology
- Congenital Heart Disease
Background:
- Anomalous left coronary artery origin arising from the pulmonary artery (ALCAPA) is a rare congenital heart defect, affecting less than 0.01% of the population.
- Symptoms typically manifest within the first 3 months of life, with high mortality without surgical repair.
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