Abstract
We present a coincidental finding of quadricuspid pulmonary valve and left pulmonary artery aneurysm. As both the pulmonary valve and the pulmonary trunk with its main branches are hard to visualise with cardiac ultrasound, most abnormalities described so far are from autopsy series. With the increasing use of CMR and its excellent potential for visualising both pulmonary valve and pulmonary arteries, we believe more cases will be discovered in the near future. Although pulmonary artery aneurysm are rare, timely detection may prevent lethal bleeding.
Avoid common mistakes on your manuscript.
A 58-year-old man was seen in our outpatient clinic after an uncomplicated ablation procedure of an AV nodal re-entry tachycardia. A routine chest X-ray revealed a dilated left pulmonary artery (Fig. 1). Physical examination was normal. Transthoracic echocardiography showed normal-sized cardiac chambers and normal systolic function of both ventricles. The main pulmonary artery had a normal diameter; however, the left and right pulmonary arteries could not be visualised. Using cardiac catheterisation, pulmonary artery hypertension was ruled out. Cardiovascular magnetic resonance imaging (CMR) demonstrated an aneurysm of the left pulmonary artery with a diameter of 47 mm, and normal diameters of the main and right pulmonary artery (24 mm and 20 mm, respectively) (Fig. 2). Furthermore a quadricuspid pulmonary valve was found with no significant stenosis and mild to moderate regurgitation (Fig. 3, Movie I–III).
Quadricuspid pulmonary valves are found in 1:250 to 1:2,500 autopsies and may be associated with other congenital abnormalities, as patent ductus arteriosus, atrial or ventricular septal defects or aortic valve abnormalities [1]. Quadricuspid pulmonary valves predominate in males and are more frequently found than quadricuspid aortic valves (with a ratio of 2:1, and 9:1, respectively) [2]. A quadricuspid pulmonary valve is usually clinically quiescent, and significant valvular stenosis or regurgitation rarely occur [3].
Aneurysm of the pulmonary arteries are also rare, found in approximately 1:14,000 autopsies [4]. Of these aneurysms 80% are located in the main pulmonary artery. Gender distribution is equal. Congenital structural heart disease (patent ductus arteriosus, atrial or ventricular septal defects, pulmonary valve stenosis) accounts for 50% of the cases of pulmonary artery aneurysm [5]. Other causes are infections (tuberculosis, mycotic infections or syphilis), connective tissue disorders (Marfan, Ehlers-Danlos), Behcets syndrome, pulmonary hypertension, atherosclerosis or trauma. In a minority of cases, no cause is identified. Local compression on adjacent structures may produce symptoms of thoracic pain, dyspnoea or cough. Rupture of the aneurysm may lead to (fatal) haemoptysis. Management of pulmonary artery aneurysm remains controversial. Early surgery has been suggested in case of symptoms or large aneurysms, especially mycotic aneurysms, which tend to rupture earlier. In idiopathic aneurysm a more conservative strategy has been advocated, as these have a lower tendency to rupture [6].
In our patient no possible causes for the aneurysm and no other congenital abnormalities were found, and it was considered idiopathic. A follow-up CMR will be performed in 6 months. To our best knowledge, only one case of quadricuspid pulmonary valve in combination with an idiopathic pulmonary artery aneurysm has been described previously [7]. In that case the aneurysm was located in the main pulmonary artery.
As both the pulmonary valve and the pulmonary trunk with its main branches are hard to visualise with cardiac ultrasound, most abnormalities described so far are from autopsy series. With the increasing use of CMR and its excellent potential of visualising both the pulmonary valve and pulmonary arteries, we believe more cases will be discovered in the near future. Although pulmonary artery aneurysms are rare, timely detection may prevent lethal bleeding.
Consent
Informed consent was obtained from the patient for publication of this case report and accompanying images. A copy of the written consent is available for review by the editor in chief of this journal.
References
Davia JE, Fenoglio JJ, DeCastro CM, et al. Quadricuspid semilunar valves. Chest. 1977;72:186–9.
Fernandez-Armenta J, Villagomez D, Fernandez-Vivancos C, et al. Quadricuspid pulmonary valve identified by transthoracic echocardiography. Echocardiography. 2009;26:288–90.
Enoch BA. Quadricuspid pulmonary valve. Br Heart J. 1968;30:67–9.
Deterling RA, Clagett OT. Aneurysm of the pulmonary artery: review of the literature and report of a case. Am Heart J. 1947;34:471–99.
Shih HH, Kang PL, Lin CY, et al. Main pulmonary artery aneurysm. J Chin Med Assoc. 2007;70:453–5.
Nair KKS, Cobanoglu AM. Idiopathic main pulmonary artery aneurysm. Ann Thorac Surg. 2001;71:1688–90.
Delicia I, Lorente G. The pulmonary valve and the pulmonary artery. Eur Heart J. 2009;30:2326.
Open Access
This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
Author information
Authors and Affiliations
Corresponding author
Electronic supplementary material
Below is the link to the electronic supplementary material.
Movie I
Cardiac magnetic resonance imaging with cine balanced steady-state free precession sequence, perpendicular to the pulmonary valve showing a quadricuspid valve. (AVI 1854 kb)
Movie II
Cardiac magnetic resonance imaging with cine balanced steady-state free precession sequence, long-axis, oblique coronal view of the quadricuspid pulmonary valve, showing mild tot moderate regurgitation. (AVI 1773 kb)
Movie III
Cardiac magnetic resonance imaging with cine balanced steady-state free precession sequence, long-axis, oblique sagittal view of the quadricuspid pulmonary valve (90° angle planned on movie II) showing mild tot moderate regurgitation. (AVI 1734 kb)
Rights and permissions
Open Access This is an open access article distributed under the terms of the Creative Commons Attribution Noncommercial License (https://creativecommons.org/licenses/by-nc/2.0), which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
About this article
Cite this article
Nollen, G.J., Kodde, J., Beek, A.M. et al. Quadricuspid pulmonary valve and left pulmonary artery aneurysm in an asymptomatic patient assessed by cardiovascular MRI. Neth Heart J 21, 196–198 (2013). https://doi.org/10.1007/s12471-011-0115-3
Published:
Issue Date:
DOI: https://doi.org/10.1007/s12471-011-0115-3