Single Coronary Artery with Fistula, Right Aortic Arch, Bicuspid Aortic Valve, and Pulmonary Stenosis: A Rare Combination

2007 ◽  
Vol 28 (4) ◽  
pp. 286-288 ◽  
Author(s):  
C.-H. Xie ◽  
Z.-Y. Zhao ◽  
Y.-B. Zhou ◽  
F.-Q. Gong
2018 ◽  
pp. bcr-2018-225309 ◽  
Author(s):  
Dominika M Zoltowska ◽  
Yashwant Agrawal ◽  
Guramrinder Singh Thind ◽  
Jagadeesh K Kalavakunta

2015 ◽  
Vol 35 (4) ◽  
pp. 434-438
Author(s):  
Hiromi KATO ◽  
Yoichi NAGATA ◽  
Yufuki TAKAGI ◽  
Yasutsugu AKINAGA ◽  
Kazunori TAKADA ◽  
...  

Surgery Today ◽  
2013 ◽  
Vol 44 (3) ◽  
pp. 550-552 ◽  
Author(s):  
Narihiro Ishida ◽  
Katsuya Shimabukuro ◽  
Yukihiro Matsuno ◽  
Hiroki Ogura ◽  
Hirofumi Takemura

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Ahmed N. Mohammad ◽  
Oghenesuvwe Eboh ◽  
Muna Mian ◽  
Rony L. Shammas

Abstract Background We report a rare case of a patient who presented with chest pain and was found to have a constellation of rare cardiac anomalies. Case presentation A 67-year-old patient with no past medical history presented with chest pain. He had mild troponin elevation, but no ischemic changes on ECG. He underwent a CT coronary angiogram for further evaluation. He was found to have a type 0 bicuspid aortic valve, large left sinus of Valsalva aneurysm and type R-III single coronary artery. These findings were confirmed with transesophageal echocardiogram and coronary angiogram. He underwent a successful repair of his aortic root aneurysm with a synthetic patch. Conclusions The combination of type R-III single coronary artery, bicuspid aortic valve, and left sinus of Valsalva aneurysm congenital anomalies in one individual is extremely rare and marks our case unique. Given the size of his Sinus of Valsalva aneurysm, the patient underwent surgical repair of his aneurysm and was asymptomatic when seen in follow-up.


1994 ◽  
Vol 24 (4) ◽  
pp. 663
Author(s):  
Yong Seog Oh ◽  
Ho Jung Youn ◽  
Wook Sung Jung ◽  
Chul Min Kim ◽  
Jang Sung Chae ◽  
...  

2019 ◽  
Vol 11 (2) ◽  
pp. 229-231
Author(s):  
Bryan J. W. Chew ◽  
Zhia N. Lim ◽  
Sanfui Yong ◽  
Robert H. Anderson ◽  
Ikenna Omeje ◽  
...  

In patients with transposition, a right aortic arch has rarely been reported among the associated malformations. When present, the arch has been obstructed because of the presence of aortic coarctation and/or arch hypoplasia. A bicuspid aortic valve is also very rare in the presence of transposition. We report here the unusual association of transposition, an unobstructed right aortic arch, and a bicuspid aortic valve in a neonate who underwent a successful arterial switch operation.


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