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Congenital: Aortic Valve
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Commentary: What can be learned from a case report, or the importance of a well-rounded education
The Journal of Thoracic and Cardiovascular SurgeryVol. 159Issue 6e343Published online: July 25, 2019- Petros V. Anagnostopoulos
Cited in Scopus: 0Quadricuspid aortic valves (QAVs) are very rare but have been well described since the early 1970s.1 Even less recognized but documented is the association of QAVs with a potential congenital structural aortopathy. In the largest series of QAVs to date, 42% of patients had ascending aortic diameters greater than or equal to 4 cm.2 Most patients with QAVs present with aortic insufficiency, aortic stenosis, or a combination of these. In this issue of the Journal, Xu and associates3 report on a 35-year-old woman who presented with a QAV associated with a ruptured sinus of Valsalva aneurysm.