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Ann Thorac Surg 2007;83:2262
© 2007 The Society of Thoracic Surgeons
a Pediatric Cardiac Surgery, Ospedale del Bambino Gesù, Piazza S. Onofrio, 4, Rome, 00165 Italy
b Pediatric Cardiology, Department of Pediatrics, University of Rome "La Sapienza", Viale Regina Elena, 324, Rome, 00161 Italy
(Email: carotti{at}opbg.net; bruno.marino{at}uniroma1.it).
We read with interest the article by Trivedi and colleagues [1] on ductal origin of the distal pulmonary artery. Authors report on a series of patients with discontinuous pulmonary arteries and ductal origin of one of them not only as an isolated lesion, but also in association with tetralogy of Fallot, pulmonary atresia with ventricular septal defect, and heterotaxy. However there is no mention in their article about the possible association of ductal origin of distal pulmonary artery with truncus arteriosus.
Such association represents a subgroup of truncus arteriosus with discontinuity of the pulmonary arteries classified by Van Praagh as truncus arteriosus type A3 [2]. In children with truncus arteriosus and left aortic arch the "duct dependent" pulmonary artery is usually the left one.
It is important to outline that the discontinuity of pulmonary arteries may complicate surgical treatment [3, 4] and follow-up [5] of patients undergoing truncus repair. Finally, in our own experience, its occurrence was mainly associated with DiGeorge-Velocardiofacial syndrome and del22q11 [6].
We believe that this association of cardiac defects deserve particular attention. Specific anatomic cardiac patterns should lead to an accurate genetic assessment of patients. On the other hand, genetic syndromes should alert clinicians on the possible presence of specific additional cardiac malformations [7] that may affect the outcome of surgical treatment.
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