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

被引:3
|
作者
Yazdi, Mehrdad Talebian [1 ]
Robbers-Visser, D. [2 ]
van der Bilt, I. A. C. [3 ]
Boekholdt, S. M. [2 ]
Koolbergen, D. R. [4 ]
Planken, R. N. [5 ]
Groenink, M. [2 ]
机构
[1] Alrijne Hosp, Dept Cardiol, Simon Smitweg 1, NL-2353 GA Leiderdorp, Netherlands
[2] Univ Amsterdam, Dept Clin & Expt Cardiol, Amsterdam UMC, Meibergdreef 9, NL-1105 BK Amsterdam, Netherlands
[3] Haga Teaching Hosp, Dept Cardiol, NL-2545 AA The Hague, Netherlands
[4] Univ Amsterdam, Dept Cardiothorac Surg, Amsterdam UMC, Meibergdreef 9, NL-1105 BK Amsterdam, Netherlands
[5] Univ Amsterdam, Acad Med Ctr, Dept Radiol & Nucl Med, Amsterdam Cardiovasc Sci, NL-1105 AZ Amsterdam, Netherlands
关键词
ALCAPA; Bland-White-Garland syndrome; Magnetic resonance imaging; Adult; Case series; ORIGIN; MANAGEMENT; ALCAPA;
D O I
10.1093/ehjcr/ytac345
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
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页数:7
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