scholarly journals Anomalous origin of circumflex coronary artery from the right pulmonary artery associated with subaortic stenosis and coarctation of the aorta

1997 ◽  
Vol 12 (4) ◽  
pp. 663-665 ◽  
Author(s):  
T Sarioglu
2020 ◽  
Vol 11 (4) ◽  
pp. 501-503
Author(s):  
Roman Sekelyk ◽  
Dmytro Kozhokar ◽  
Andrii Kurkevych ◽  
Oleksandra Motrechko ◽  
Illya Yemets

We present a patient with the extremely rare coexistence of two distinct coronary artery malformations: anomalous aortic origin of the right coronary artery from the left aortic sinus with intramural course and anomalous origin of the circumflex coronary artery from the right pulmonary artery. Surgical reimplantation of the anomalous left circumflex coronary artery to the aorta and unroofing of the intramural portion of the anomalous right coronary artery were performed.


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.


2017 ◽  
Vol 25 (7-8) ◽  
pp. 528-530 ◽  
Author(s):  
Ahmet Daylan ◽  
Serkan Ertugay ◽  
Anıl Ziya Apaydın ◽  
Emrah Oğuz

Anomalous origin of the circumflex coronary artery from the right pulmonary artery is rare, and symptoms are related to the collateralization and amount of myocardium that it supplies. A 50-year-old woman with severe bicuspid aortic valve stenosis had the diagnosis of anomalous origin of the circumflex coronary artery from the right pulmonary artery before valve replacement. Ligation and division of the circumflex coronary artery was performed. Myocardial ischemia was not observed. The patient was discharged after an uneventful recovery.


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.


1978 ◽  
Vol 76 (2) ◽  
pp. 190-194 ◽  
Author(s):  
David A. Ott ◽  
Denton A. Cooley ◽  
William W. Pinsky ◽  
Charles E. Mullins

2004 ◽  
Vol 78 (1) ◽  
pp. 324-326 ◽  
Author(s):  
Anil Sivadasan Radha ◽  
Baiju Sasi Dharan ◽  
Raman Krishna Kumar ◽  
Suresh Gururaja Rao

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