Origin of left coronary artery from right pulmonary artery co-existing with coarctation of the aorta

1990 ◽  
Vol 27 (1) ◽  
pp. 31-36 ◽  
Author(s):  
Solomon E. Levin ◽  
Raymond Dansky ◽  
Robin H. Kinsley
2004 ◽  
Vol 78 (1) ◽  
pp. 324-326 ◽  
Author(s):  
Anil Sivadasan Radha ◽  
Baiju Sasi Dharan ◽  
Raman Krishna Kumar ◽  
Suresh Gururaja Rao

2015 ◽  
Vol 26 (4) ◽  
pp. 802-804
Author(s):  
Xuecun Liang ◽  
Lin Wu

AbstractIn this study, we describe a very rare case of anomalous left coronary artery arising from the right pulmonary artery in association with coarctation of the aorta. A 3-month-old boy presented with refractory congestive heart failure since 20 days after birth. The initial echocardiography suggested the diagnosis of left coronary artery-to-right pulmonary artery fistula associated with coarctation; however, selective coronary angiography demonstrated the rare anomaly of the left coronary artery arising from the right pulmonary artery. Subsequently, he underwent successful transcatheter balloon angioplasty for aortic coarctation and surgical repair of left coronary artery re-implantation.


2017 ◽  
Vol 27 (9) ◽  
pp. 1853-1856
Author(s):  
Ziyad M. Binsalamah ◽  
Diego A. Lara ◽  
Emmett D. McKenzie

AbstractAnomalous origin of the left coronary artery from the right pulmonary artery in single ventricles is a very rare congenital anomaly. Failure to recognise it preoperatively may lead to adverse outcomes, including death. We report the case of a neonate with a univentricular heart in the form of a double-outlet right ventricle, mitral atresia with discrete coarctation of the aorta, and an incidental intraoperative finding of an anomalous origin of the left coronary artery from the right pulmonary artery. The patient underwent a successful repair with an uneventful postoperative course.


2019 ◽  
Vol 10 (4) ◽  
pp. 508-512
Author(s):  
Vishal Agrawal ◽  
Nikunj Vaidhya ◽  
Mrinal Patel ◽  
Amit Mishra ◽  
Dinesh Patel

Anomalous origin of the left coronary artery (LCA) from the right pulmonary artery (ALCARPA) is an extremely rare subset of an already rare entity, anomalous origin of the LCA from the pulmonary artery. Whenever it is diagnosed preoperatively, one should be extremely vigilant about the potential intramural course of the descending part of the LCA in the aorta. Preoperative imaging frequently fails to delineate this intramural course. We report our experience with one such case where we had accidentally injured the LCA during dissection from the right pulmonary artery. Although it was successfully managed, it reinforces our aforementioned point concerning the importance of vigilance in seeking to identify intramurality as a component of this anomaly of coronary artery origin.


2008 ◽  
Vol 85 (2) ◽  
pp. 675-677 ◽  
Author(s):  
Iki Adachi ◽  
Koji Kagisaki ◽  
Toshikatsu Yagihara ◽  
Ikuo Hagino ◽  
Toru Ishizaka ◽  
...  

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