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Letter to the Editor

Published online by Cambridge University Press:  20 November 2006

Gerardo Piacentini ,
Silvia Placidi  and
Bruno Marino
Gerardo Piacentini
Affiliation:
Pediatric Cardiology, Department of Pediatrics, University of Rome “La Sapienza”, Italy
Silvia Placidi
Affiliation:
Pediatric Cardiology, Department of Pediatrics, University of Rome “La Sapienza”, Italy
Bruno Marino
Affiliation:
Pediatric Cardiology, Department of Pediatrics, University of Rome “La Sapienza”, Italy
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Abstract

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Type
Letter to the Editor
Information
Cardiology in the Young , Volume 16 , Issue 6 , December 2006 , pp. 608
Copyright
© 2006 Cambridge University Press

Sir,

Re: Right isomerism, pulmonary atresia, and major aorto-pulmonary collateral arteries.

We read with interest the recent report by Kumar et al.1 on the association of major aorto-pulmonary collateral arteries with right isomerism. Major aorto-pulmonary collateral arteries, with or without discontinuity of the intrapericardial pulmonary arteries, are quite rare in patients with right isomerism. They are seen far more frequently in the subset of children with pulmonary atresia with ventricular septal defect in which the intracardiac anatomy is that of tetralogy of Fallot.2 Aorto-pulmonary collateral arteries, in fact, are reported to exist in up to one-tenth of cases of right isomerism, or visceral heterotaxy with asplenia.3, 4 Even in children with pulmonary atresia and right isomerism, the collateral arteries are not as rare as in patients with pulmonary atresia when the ventricular septum is intact.5, 6 Arterial supply to the lungs through bilateral arterial ducts is also encountered more frequently in patients with right isomerism than in those with pulmonary atresia and an intact ventricular septum.4, 7, 8 In our experience, when major aorto-pulmonary collateral arteries have been seen in the setting of right isomerism and pulmonary atresia, the intracardiac anatomy has always been that of an anterior aorta arising from the morphologically right ventricle supported by a muscular infundibulum, in other words the “transposition” rather than the “tetralogy” variant.4, 7, 9

In children with right isomerism and pulmonary atresia, the complexity of pulmonary arterial supply suggests an early morphogenesis of the pulmonary obstruction. Whilst we might also suspect the possible involvement of deficiencies of the neural crest and/or branchial arches, we would then expect the intracardiac anatomy to be that of tetralogy, rather than an anterior aorta supported by a complete muscular infundibulum. From the clinical point of view, the frequency of complex patterns of pulmonary arterial supply associated with the presence of totally anomalous pulmonary venous connection, often obstructed, suggests that accurate pre-operative diagnosis, showing all vascular extracardiac structures, is essential.1, 4, 9 In this light, while recognising the significant progress made recently in use of helical computed tomography,10 we still consider that angiocardiography is necessary.9

References

Kumar S, Ansari J, Weerasena N. A rare association of major aorto-pulmonary collaterals with right isomerism and totally anomalous pulmonary venous drainage. Cardiol Young 2005; 15: 643–646.Google Scholar
Thiene G, Bortolotti U, Gallucci V, Valente ML, Dalla Volta S. Pulmonary atresia with ventricular septal defect: further anatomical observations. Br Heart J 1977; 39: 1223–1233.Google Scholar
Uemura H, Ho SY, Devine WA, Kilpatrick LL, Anderson RH. Atrial appendages and venoatrial connections in hearts from patients with visceral heterotaxy. Ann Thorac Surg 1995; 60: 561–569.Google Scholar
Vitiello R, Moller JH, Marino B, Vairo U, Edwards JE, Titus JL. Pulmonary circulation in pulmonary atresia associated with the asplenia cardiac syndrome. J Am Coll Cardiol 1992; 20: 363–365.Google Scholar
Zuberbuhler JR, Anderson RH, Morphological variations in pulmonary atresia with intact ventricular septum. Br Heart J 1979; 41: 281–288.Google Scholar
Albanese SB, Carotti A, Toscano A, Marino B, Di Donato RM. Pulmonary atresia with intact ventricular septum and systemic-pulmonary collateral arteries. Ann Thorac Surg 2002; 73: 1322–1324.Google Scholar
Formigari R, Vairo U, De Zorzi A, Santoro G, Marino B. Prevalence of bilateral ductus arteriosus in patients with pulmonic valve atresia and asplenia syndrome. Am J Cardiol 1992; 70: 1219–1220.Google Scholar
Milanesi O, Daliento L, Thiene G. Solitary aorta with bilateral ductal origin of non-confluent pulmonary atresia with intact ventricular septum. Int J Cardiol 1990; 29: 90–92.Google Scholar
Marino B, Corno A, Pasquini L, et al. Indication for systemic to pulmonary artery shunts guided by two-dimensional and Doppler echocardiography. Criteria for patients selection. Ann Thorac Surg 1987; 44: 495.Google Scholar
Shiraishi I, Yamagishi M, Iwasaki N, Toiyama K, Hamaoka K. Helical computed tomographic angiography in obstructed total anomalous pulmonary venous drainage. Ann Thorac Surg 2001; 71: 1690–1692.Google Scholar