Anomalous coronary artery from the pulmonary artery diagnosed in adulthood: a case series on variations of coronary anatomy and the diagnostic value of cardiac magnetic resonance imaging

Author:

Talebian Yazdi Mehrdad1ORCID,Robbers-Visser D2,van der Bilt I A C3,Boekholdt S M2,Koolbergen D R4,Planken R N5,Groenink M2

Affiliation:

1. Department of Cardiology, Alrijne Hospital , Simon Smitweg 1, 2353 GA Leiderdorp , The Netherlands

2. Department of Clinical and Experimental Cardiology, Amsterdam UMC, University of Amsterdam , Meibergdreef 9, 1105 BK Amsterdam , The Netherlands

3. Department of Cardiology, Haga Teaching Hospital , 2545 AA the Hague , The Netherlands

4. Department of Cardiothoracic Surgery, Amsterdam UMC, University of Amsterdam , Meibergdreef 9, 1105 BK Amsterdam , The Netherlands

5. Department of Radiology and Nuclear Medicine, Amsterdam UMC, Academic Medical Center, Amsterdam Cardiovascular Sciences, University of Amsterdam , 1105 AZ Amsterdam , The Netherlands

Abstract

Abstract Background Anomalous coronary artery from the pulmonary artery is a rare congenital disorder with high mortality rates in infancy. Adult cases can present with life-threatening arrhythmias and sudden cardiac death. Case summary We report three cases of adults with anomalous pulmonary origin of each of the main coronary branches. The first patient with an anomalous left coronary artery from the pulmonary artery presented with an out-of-hospital cardiac arrest. The second patient with an anomalous circumflex artery from the pulmonary artery was evaluated for a bicuspid aortic valve and a suspected coronary fistula but was otherwise asymptomatic. The third patient with an anomalous right coronary artery from the pulmonary artery presented with anginal symptoms. In all cases, the diagnosis was made by cardiac computed tomography or coronary angiography. Cardiac magnetic resonance imaging was performed in all patients to guide clinical decision making on surgical or non-invasive management. All patients underwent surgical repair. In two patients, a dual coronary artery system was restored by aortic reimplantation of the anomalous coronary artery. In one patient, aortic reimplantation was unsuccessful due to poor vessel quality and the anomalous coronary artery was ligated. Clinical follow-up during 1.8–9.7 years did not show any cardiovascular complications and all patients are currently alive and asymptomatic. Discussion Anomalous coronary artery from the pulmonary artery can have various clinical presentations in adulthood. Cardiac magnetic resonance imaging is a useful modality to guide selection of patients who might have symptomatic or prognostic benefit from surgical repair.

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine

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