| Literature DB >> 23336304 |
Pierre O Dionne1, Nancy Poirier, Jessica Forcillo, Louis M Stevens, Carl Chartrand-Lefebvre, Samer Mansour, Nicolas Noiseux.
Abstract
Anomalous origin of left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital anomaly that causes a left-to-right shunt via the coronary system, resulting in coronary steal. We report an unusual case of a healthy 48 years-old patient presenting with dyspnea on exertion and mild chest pain who underwent surgical correction of this rare anomaly. Multiple procedures have been proposed in adults with ALCAPA. Although re-implantation of the left main coronary artery (LMCA) to the aorta remains the most physiological correction for this anomaly, the combination of LMCA ligation and coronary artery bypass grafting provides a dual coronary flow system and is preferable when re-implantation is impossible.Entities:
Mesh:
Year: 2013 PMID: 23336304 PMCID: PMC3554424 DOI: 10.1186/1749-8090-8-15
Source DB: PubMed Journal: J Cardiothorac Surg ISSN: 1749-8090 Impact factor: 1.637
Figure 1CTA 3D reconstruction of the heart. Aorta (AO), Right coronary artery (RC), acute marginal (AM), pulmonary artery (PA) and left anterior descending artery (LAD).
Figure 2CABG Coronary artery bypass grafting (CABG) of the left anterior descending artery (LAD) with a saphenous vein (SV) graft. Acute marginal (AM). Patient’s head up.