scholarly journals Single coronary artery with bicuspid aortic valve

2018 ◽  
pp. bcr-2018-225309 ◽  
Author(s):  
Dominika M Zoltowska ◽  
Yashwant Agrawal ◽  
Guramrinder Singh Thind ◽  
Jagadeesh K Kalavakunta
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 ◽  
...  

Choonpa Igaku ◽  
2006 ◽  
Vol 33 (1) ◽  
pp. 75-81
Author(s):  
Hiroko ISHIGAMI ◽  
Masatsugu IWASE ◽  
Keiko HYOUDO ◽  
Idumi AOYAMA ◽  
Mamoru ITO ◽  
...  

2021 ◽  
Vol 10 (14) ◽  
pp. 3070
Author(s):  
Gudrun Feuchtner ◽  
Sven Bleckwenn ◽  
Leon Stoessl ◽  
Fabian Plank ◽  
Christoph Beyer ◽  
...  

(1) Background. Bicuspid aortic valve (BAV) is associated with genetic defects (NOTCH 1, GATA 5) and aortopathy. Differences in the flow patterns and a genetic predisposition could also affect coronary arteries. The objective was to assess the coronary artery calcium score (CACS) and coronary artery disease (CAD) burden by coronary computed tomography angiography (CTA) in patients with BAV stenosis, as compared to stenotic tricuspid aortic valves (TAV). (2) Methods. A retrospective case–control study. A total of 47 patients with BAV stenosis (68.9 years ± 12.9, 38.3% females) who underwent CTA were matched with 47 TAV stenosis patients for age, gender, smoking, arterial hypertension, dyslipidemia, diabetes, body-mass-index and chronic kidney disease. (3) Results. The coronary artery calcium score (CACS) was lower in BAV (237.4 vs. 1013.3AU; p < 0.001) than in TAV, and stenosis severity was less (CAD-RADTM: p < 0.001). More patients with BAV had CACS zero (27.7% vs. 0%; p < 0.001). The majority (68.1%) of patients with BAV had no or non-obstructive CAD but only 25.5% of TAV (p < 0.001). Obstructive CAD (>50% stenosis) by CTA was more frequently observed in patients with TAV (68.1%; p < 0.001). (4) Conclusions and Relevance. Patients with BAV stenosis have markedly less coronary calcium and less severe coronary stenosis. CTA succeeds to rule out obstructive CAD in the majority of BAV, with adherent implications for TAVR planning.


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