The rare coexistence of a type II double left anterior descending artery and partial ARCAPA potentially limited ischemic burden in an asymptomatic 51-year-old patient.
Highlights the rare coexistence of partial ARCAPA and dual LAD, emphasizing the role of CCTA in diagnosing complex congenital coronary anomalies.
Absolute Event Rate: 0% vs 0%
This case report highlights the coexistence of two rare coronary artery anomalies assessed by computed coronary tomography angiography (CCTA). We present the case of a 51-year-old hypertensive patient with a type II double left anterior descending artery (LAD) and an anomalous infundibular branch originating from the pulmonary artery (partial ARCAPA). This association may have contributed to a limited ischemic burden, explaining the patient’s asymptomatic state. Knowledge of these rare coronary anatomies is essential for accurate diagnosis and management.
Morelli et al. (Tue,) reported a other. The rare coexistence of a type II double left anterior descending artery and partial ARCAPA potentially limited ischemic burden in an asymptomatic 51-year-old patient.