1. A patient with single coronary artery, bicuspid aortic valve and sinus of Valsalva aneurysm
- Author
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Ahmed N. Mohammad, Oghenesuvwe Eboh, Rony L. Shammas, and Muna R. Mian
- Subjects
lcsh:Diseases of the circulatory (Cardiovascular) system ,medicine.medical_specialty ,Bicuspid aortic valve ,Sinus of Valsalva aneurysm ,Case Report ,030204 cardiovascular system & hematology ,Transesophageal echocardiogram ,Chest pain ,Asymptomatic ,030218 nuclear medicine & medical imaging ,03 medical and health sciences ,0302 clinical medicine ,Aneurysm ,Internal medicine ,medicine ,cardiovascular diseases ,Sinus (anatomy) ,Past medical history ,medicine.diagnostic_test ,business.industry ,Single coronary artery ,medicine.disease ,Cardiac surgery ,medicine.anatomical_structure ,Congenital heart defects ,lcsh:RC666-701 ,cardiovascular system ,Cardiology ,medicine.symptom ,Cardiology and Cardiovascular Medicine ,business - 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.
- Published
- 2021