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CASE REPORT
Year : 2016  |  Volume : 6  |  Issue : 1  |  Page : 10

Quadricuspid Aortic Valve: A Rare Congenital Cause of Aortic Insufficiency


1 Department of Internal Medicine, St. Joseph's Regional Medical Center, 07503 NJ, USA
2 Department of Cardiology, St. Joseph's Regional Medical Center, 07503 NJ, USA

Correspondence Address:
Rahul Vasudev
Department of Internal Medicine, St. Joseph's Regional Medical Center, 703 Main Street Paterson, 07503 NJ
USA
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/2156-7514.179417

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Quadricuspid aortic valve (QAV) is a rare congenital cardiac anomaly causing aortic regurgitation usually in the fifth to sixth decade of life. Earlier, the diagnosis was mostly during postmortem or intraoperative, but now with the advent of better imaging techniques such as transthoracic echocardiography, transesophageal echocardiography (TEE), and cardiac magnetic resonance imaging, more cases are being diagnosed in asymptomatic patients. We present a case of a 39-year-old male who was found to have QAV, with the help of TEE, while undergoing evaluation for a diastolic murmur. The patient was found to have Type B QAV with moderate aortic regurgitation. We also present a brief review of classification, pathophysiology, and embryological basis of this rare congenital anomaly. The importance of diagnosing QAV lies in the fact that majority of these patients will require surgery for aortic regurgitation and close follow-up so that aortic valve replacement/repair is done before the left ventricular decompensation occurs.


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