High Risk Reoperation Reveals an Anomalous Right Coronary Artery from the Pulmonary Artery

Résumé fourni par la source

This case describes a patient with complex congenital heart defects and a symptomatic undiagnosed anomalous right coronary artery from the pulmonary artery (ARCAPA) that led to progressive right ventricular failure. Clinical deterioration led to a decision for a high-risk corrective reoperation, which finally established the presence of an ARCAPA after initial diagnostic challenges.

Ce résumé expose les affirmations des auteurs. BNTIC ne l’interprète pas comme une validation indépendante des résultats.