|Number 13-13: Quadricuspid pulmonary valve accompanied by pulmonary trunk and left pulmonary artery|
Number 13-13: Quadricuspid pulmonary valve accompanied by pulmonary trunk and left pulmonary artery aneurysm
Case from: Kaoru Tanaka M.D., PhD1, Guy Van Camp M.D., PhD2, Douwe E Verdries M.D. 1, Johan De Mey M.D., PhD1
Institute: Department of Radiology1 and Department of Cardiology2, UZ Brussel, Brussels, Belgium
Clinical history: A 40 year-old male with no significant past medical history was referred for a chest CT due to the discovery of an enlarged pulmonary artery on routine chest x-ray. The patient was minimally symptomatic but complained of chest heaviness when lying on his left side. A grade III/VI systolic murmur was auscultated over the pulmonary artery.
Figure 1 Contrast enhanced chest CT showing dilated pulmonary trunk and left main pulmonary artery extending to the distal left pulmonary artery
Figure 2 Chest CT showing mosaic perfusion in the left upper lobe due to the dilated pulmonary artery
A non-ECG gated chest computed tomography (CT) with contrast showed dilated pulmonary trunk (up to 48mm) and left pulmonary artery (up to 46mm) extending to the distal left pulmonary artery (Figure 1). Chest CT also showed mosaic perfusion in the left upper lobe due to the dilated pulmonary artery (Figure 2).
Movie 1: RVOT cine by CMR demonstrates Movie 2: Pulmonary valve cine imaging shows
severe dilatation of the pulmonary trunk and left a quadricuspid pulmonary valve.
pulmonary artery, accelerated flow through the
pulmonary valve, and pulmonary regurgitation.
Right ventricular outflow tract (RVOT) cine view by CMR (Philips Achieva 1.5 T) demonstrated severe dilatation of pulmonary trunk and left pulmonary artery, accelerated flow through the pulmonary valve, and pulmonary regurgitation (Movie 1). Subsequent pulmonary valve cine imaging showed a quadricuspid pulmonary valve (Movie 2). The anterior and the right cusp were equal in size and the left cusp was divided into two smaller cusps.
Figure 3: CMR flow quantification showing mild pulmonary stenosis with maximum velocity of 3.3 m/sec and moderate pulmonary regurgitation with regurgitant fraction of 30%
The flow quantification showed a mild pulmonary stenosis with maximum velocity of 3.3 m/sec and mild pulmonary regurgitation with a regurgitant fraction of 30% (Figure 3). This corresponded to the echo findings
Movie 3: The four chambers cine imaging shows
The four chambers cine imaging showed normal right and left ventricular systolic function, mild tricuspid regurgitation, slightly prominent RV trabeculations, and a dilated distal branch of the left pulmonary artery (Movie 3). No other congenital abnormalities, such as patent ductus arteriosis, atrial septal defect or ventricular septal defect were found.
Conclusion & Perspective: The anatomy of the pulmonary valve is difficult to assess by echocardiography. The quadricuspid pulmonary valve (QPV) has been considered to be a relatively rare congenital anomaly (from 1 in 400 to 2,000 autopsies), though there have been more case reports published in the last 5 years due to the increase use of CMR and ECG-gated CT. Our case demonstrates both mild pulmonary stenosis and regurgitation, but a QPV is usually clinically benign.
The pulmonary aneurysm has also been considered to be uncommon (1 in 14,000 autopsies). However, three case reports of the QPV with the pulmonary aneurysm have been published since 2009: two cases of QPV and idiopathic pulmonary aneurysm1, 2, and one case of QPV with post-stenotic dilatation of the pulmonary artery3. Nollen et al have well described that the pulmonary aneurysm might be accompanied by congenital heart disease, infectious disease, connective tissue disease, Behcets syndrome, pulmonary hypertension, trauma and atherosclerosis2.
A large pulmonary aneurysm needs to be carefully monitored as this could be a cause of a sudden death by rupture, though there are no clinical guidelines for the management of these aneurysms as yet. Muthialu et al has reported a case with successful operation for an idiopathic pulmonary aneurysm of 6cm, and concluded that it is wise to consider intervention for larger asymptomatic aneurysms4.
The excellent visualization of pulmonary valve by CMR will surely enable the discovery of more live cases with QPV. In this setting, the presence of other congenital abnormalities or aortic valve disease should always be ruled out. CMR also allows to monitor the size of the pulmonary artery. Equally, the patient with pulmonary aneurysm should always be assessed by CMR to exclude abnormal anatomy of the pulmonary valve or any other underlying pathologies.
1. Delicia I, Lorente G. The pulmonary valve and the pulmonary artery. Eur Heart J. 2009 Oct; 30(19):2326.
2. Olivares-Reyes A, Molina-Bello E, Espinola-Zavaleta N. Congenital quadricuspid pulmonary valve in an adult patient with double valvular lesions and poststenotic dilatation of the trunk and the left branch of the pulmonary artery: a case presentation and review of the literature. Congenit Heart Dis. 2012 Nov-Dec; 7(6): E103-8.
3. Nollen GJ, Kodde J, Beek AM, Res JC, van Rossum AC. Quadricuspid pulmonary valve and left pulmonary artery aneurysm in an asymptomatic patient assessed by cardiovascular MRI. Neth Heart J. 2013 Apr; 21(4):196-8.
4. Muthialu N, Raju V, Muthubaskaran V, Chandrasekar P, Muralidharan S, Kuppanna PJ. Idiopathic pulmonary artery aneurysm with pulmonary regurgitation. Ann Thorac Surg. 2010 Dec;90(6):2049-51.
COTW handling editor: Monica Deac
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