Abstract Background Anomalous left coronary artery from the pulmonary artery (ALCAPA) is a very rare, congenital condition. Patients typically exhibit symptoms within the first few weeks of life. “Adult-type ALCAPA”, which presents later in life, is even rarer and is mostly detected due to symptoms of heart failure or after life-threatening arrhythmias. Case Summary We present the case of a 53-year-old asymptomatic male, who was incidentally diagnosed with adult-type ALCAPA during a coronary computed tomography angiography (CCTA) screening performed for cardiac risk stratification. Further cardiac investigations included echocardiography, myocardial perfusion scintigraphy, invasive coronary angiography (ICA), and cardiac magnetic resonance imaging (CMRI). As he had never experienced any cardiac symptoms at rest or during exercise throughout his life, the patient has not yet decided to undergo the recommended cardiac surgery. The patient is currently seeking a second opinion. Discussion ALCAPA is rare, but the increased use of CCTA for risk stratification in asymptomatic patients might lead to more frequent diagnosis in older individuals. As with our patient, a dilemma may arise when deciding on its treatment, because the guideline-recommended treatment is surgical correction in all patients. However, there is still little evidence to support this recommendation for older, asymptomatic patients, making advice and decisions difficult for such individuals.
Jöbstl et al. (2025) studied this question.