| Literature DB >> 26382034 |
Leire Unzué1, Eulogio García2, Francisco Javier Parra3, Jesús Palomo4, Leticia Fernández Friera2, Jorge Solís2.
Abstract
Congenital atresia of the left main coronary artery (LMCA) is one of the rarest congenital anomalies, which may have an unfavorable prognosis leading to myocardial ischemia, ventricle dysfunction or even sudden cardiac death. There are 34 cases of LMCA in adults reported in the literature, most of them successfully treated with coronary revascularization. We report the case of an adult with LMCA who presented with terminal heart failure that required biventricular assistance and heart transplant. Published by Elsevier Inc.Entities:
Keywords: Coronary artery anomaly; Left main coronary artery atresia
Mesh:
Year: 2015 PMID: 26382034 DOI: 10.1016/j.carrev.2015.08.006
Source DB: PubMed Journal: Cardiovasc Revasc Med ISSN: 1878-0938