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So-called “absence” of the leaflets of the pulmonary valve

Published online by Cambridge University Press:  30 June 2008

Philippe Acar*
Affiliation:
Children Hospital, Pediatric Cardiology, Toulouse, France
Sylvia Abadir
Affiliation:
Children Hospital, Pediatric Cardiology, Toulouse, France
Gilles Brierre
Affiliation:
Children Hospital, Pediatric Cardiology, Toulouse, France
*
Correspondence to: Ph Acar, Cardiologie Pédiatrique, Hôpital des Enfants, 330 av de Grande-Bretagne, 31000 Toulouse, France. Tel: +33-5-34-55-87-15; Fax: +33-5-34-86-63; E-mail: acar.p@chu-toulouse.fr
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Abstract

Type
Images in Congenital Cardiac Disease
Copyright
Copyright © Cambridge University Press 2008

A neonate who had systolic and diastolic murmurs was referred to our institution for investigation of moderate cyanosis without respiratory distress. Cross-sectional echocardiography showed a large ventricular septal defect opening beneath the ventricular outlets. The short axis parasternal view (Fig. 1), revealed that the subpulmonary infundibulum, arising from the right ventricle (RV), coursed through a hypoplastic ventriculo-pulmonary junction (PV) to capacious left (LPA) and right (RPA) pulmonary arteries. Colour Doppler interrogation revealed severe pulmonary regurgitation. Three-dimensional echocardiography was performed using the paediatric matrix probe (2–7 MHz). The same view (Fig. 2) characterized the specific anatomy of the rudimentary formation of the leaflets of the pulmonary valve, an arrangement usually described as “absent pulmonary valve”. Viewed from below, the remnants of the valve were seen to be composed of thick nodular tissue, without demarcation of true leaflets or zones of apposition. The arrow indicates the eccentric and regurgitant orifice. The left (LPA) and right (RPA) pulmonary arteries were massively dilated. This patient, who is waiting for surgical correction, illustrates well the features of absent pulmonary valve syndrome,Reference Zucker, Rozin, Levitas and Zalzstein1 in reality rudimentary formation of the valvar tissue, which can be demonstrated well by transthoracic three-dimensional echocardiography.

Figure 1

Figure 2

References

1. Zucker, N, Rozin, I, Levitas, A, Zalzstein, E. Clinical presentation, natural history, and outcome of patients with the absent pulmonary valve syndrome. Cardiol Young 2004; 14: 402408.CrossRefGoogle ScholarPubMed
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