@article{ajmcr202081224,
author={{Chandrakumar, Harshith Priyan and Patwa, Karishma and Chowdhury, Yuvraj Singh and Shetty, Mrinali and Goel, Ridhima and Otey, Jennifer and Awwad, Ahmed and Salifu, Moro O. and McFarlane, Samy I.},
title={Anomalous Origins of All Three Coronary Arteries from Separate Ostia within the Right Aortic Cusp: A Case Report and Review of the Literature},
journal={American Journal of Medical Case Reports},
volume={8},
number={12},
pages={518--521},
year={2020},
url={http://pubs.sciepub.com/ajmcr/8/12/24},
issn={2374-216X},
abstract={Coronary artery anomalies are congenital defects which are found incidentally or after cardiac events. While these are rare abnormalities with the majority of patients remain asymptomatic and largely undiagnosed, it remains to be a major cause of sudden cardiac death (SCD). Anomalous origin of left coronary artery (ALCA) from the opposite right aortic sinus is extremely rare with less than 100 cases reported to-date. These patients are at increased risk for significant cardiac events, including SCD. In this report, we present a 48-year-old man with hypertension and marijuana use who was admitted initially with multi-lobar pneumonia and acute kidney injury, developed respiratory failure and sustained ST elevation myocardial infarction (STEMI). Coronary angiography demonstrated anomalous origin of all three main coronary arteries arising from right aortic sinus. In this report we also discuss the genesis of this rare and potentially fatal congenital abnormality and we highlight the diagnostic and management strategies available to-date.},
doi={10.12691/ajmcr-8-12-24}
publisher={Science and Education Publishing}
}