Türk Kardiyoloji Derneği Arşivi (Sep 2015)

A rare coronary anomaly with masked diagnosis: Anomalous left circumflex artery from right pulmonary artery

  • Doğukan Aktaş,
  • Abdullah Erdem,
  • Nida Çelik,
  • Hacer Kamalı,
  • Turkay Sarıtaş

DOI
https://doi.org/10.5543/tkda.2015.94399
Journal volume & issue
Vol. 43, no. 6
pp. 551 – 553

Abstract

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Anomalous origin of the circumflex coronary artery from the pulmonary artery is a rare congenital coronary anomaly. While it generally follows an asymptomatic course, if undiagnosed it may lead to severe clinical outcomes, including sudden death. The condition can be masked by associated defects, so when it is clinically suspected, diagnosis must be confirmed by conventional and/ or magnetic resonance angiography, even if echocardiography clearly shows coronary roots. This report describes a patient who underwent neonatal surgery for aortic coarctation and was diagnosed with coronary artery anomaly at 15 months old.

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