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The Journal of Thoracic and Cardiovascular Surgery, Vol 72, 33-38, Copyright © 1976 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
F Ando, H Shirotani, J Kawai, Y Kanzaki and N Setsuie
A one-stage total repair was successfully accomplished in a Japanese girl,
7 years, 8 months old, who had asplenia syndrome with vixceral heterotaxia,
isolated levocardia, and complicated cardiovascular anomalies;
double-outlet right ventricle with d-malposition of the great arteries
(anterior aorta, posterior pulmonary trunk), complete form of endocardial
cushion defect, total anomalous pulmonary venous drainage, pulmonary
stenosis, sinus venosus type of atrial septal defect, patent ductus
arteriosus, bilateral superior venae cavae, and inferior vena cava draining
into the left-sided atrium. A routine cardiopulmonary bypass, consisting of
ligations of the patent ductus arteriosus and right superior vena cava, was
followed by direct and patch closure of atrial and ventricular septal
defects. An internal conduit was inserted to drain the systemic venous
blood from the left ventricle to the pulmonary artery. Thus a total repair
is physiologically possible in such complicated cardiovascular anomalies
with an asplenia syndrome. One year after this operation the child is well
and attends school daily.
ARTICLES
Successful total repair of complicated cardiac anomalies with asplenia syndrome
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