2012
DOI: 10.1097/rti.0b013e31822e864c
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Quadricuspid Pulmonary Valve

Abstract: Quadricuspid pulmonary valve (QPV) is a rare congenital cardiac entity. The recognition of QPV has clinical significance as it can cause pulmonary valve dysfunction. It is also important to recognize this condition in patients undergoing the Ross procedure. We report a case of QPV diagnosed by computed tomography with associated pulmonary stenosis and right ventricular hypertrophy.

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Cited by 11 publications
(6 citation statements)
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“…Quadricuspid pulmonic valve (QPV) is a rare congenital anomaly, occurring in approximately 1 in 400 to 1 in 2,000 people, with a 2:1 male to female ratio [ 1 , 2 ]. Unlike a bicuspid pulmonary valve, it rarely presents with clinical complications, such as valvular insufficiency or stenosis, and thus, it is most often a post-mortem finding [ 1 , 3 , 4 ].…”
Section: Introductionmentioning
confidence: 99%
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“…Quadricuspid pulmonic valve (QPV) is a rare congenital anomaly, occurring in approximately 1 in 400 to 1 in 2,000 people, with a 2:1 male to female ratio [ 1 , 2 ]. Unlike a bicuspid pulmonary valve, it rarely presents with clinical complications, such as valvular insufficiency or stenosis, and thus, it is most often a post-mortem finding [ 1 , 3 , 4 ].…”
Section: Introductionmentioning
confidence: 99%
“…Unlike a bicuspid pulmonary valve, it rarely presents with clinical complications, such as valvular insufficiency or stenosis, and thus, it is most often a post-mortem finding [ 1 , 3 , 4 ]. Due to the common congenital origins of these two anomalies, a QPV is frequently associated with aortic valve anomalies; however, unlike a quadricuspid aortic valve, which often leads to stenosis or insufficiency, a four-leaflet pulmonary valve appears to have no negative consequences on pulmonary circulation [ 2 - 4 ]. To date, only two cases of QPV with stenosis have been reported, and the literature has described rare cases with evidence of pulmonary regurgitation and/or hypertension [ 4 , 5 ].…”
Section: Introductionmentioning
confidence: 99%
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“…Except for five cases diagnosed using TTE, adult patients associated with other congenital heart diseases except for pulmonary stenosis were diagnosed using contrast CT scan or CMR after 2009 [ 13 - 16 ]. As with TTE, the frequency of valve morphology in cases diagnosed using CT scan or CMR was largely different from that in cases diagnosed at autopsy (Table 3 ) [ 13 - 16 , 40 - 55 ]. It might be reasonable to actively look for QPV in patients who have marked aneurysmal dilatation of the main pulmonary artery, with or without an extension of the dilatation into pulmonary artery branches [ 54 ].…”
Section: Discussionmentioning
confidence: 90%