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The Annals of Thoracic Surgery, Vol 35, 132-137, Copyright © 1983 by The Society of Thoracic Surgeons
DF Shore, SY Ho, RH Anderson, M de Leval and C Lincoln
Three patients are described in whom an aortopulmonary septal defect
(aortopulmonary window) coexisted with a ventricular septal defect and
pulmonary atresia. One patient had mild and another, moderate aortic
regurgitation. In addition, one patient had a sinus of Valsalva aortic
aneurysm, while another had a single coronary artery arising from the
pulmonary trunk. One patient underwent surgical correction in infancy; the
other two, in early adult life. In all three patients, surgical correction
involved closure of the aortopulmonary window, closure of the ventricular
septal defect, and placement of a valved conduit between the right
ventricle and the distal pulmonary trunk. One patient died 3 weeks
postoperatively due to secondary hemorrhage where the conduit had been
sutured to the right ventricle. The other two patients are alive and well 3
1/2 years and 6 months after surgery, respectively. The presence of
aortopulmonary window permits normal development of the pulmonary arteries
in the presence of the coexisting pulmonary atresia; in the three patients
described, the absence of pulmonary vascular disease made total surgical
repair feasible for this combination of defects.
ARTICLES
Aortopulmonary septal defect coexisting with ventricular septal defect and pulmonary atresia
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