2011
DOI: 10.1007/s11748-010-0691-y
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Reconstruction of nonconfluent pulmonary artery using the retroaortic innominate vein for a single ventricle

Abstract: The innominate vein usually courses anterior to the aortic arch, where it joins the right brachiocephalic vein to form the superior caval vein. A retroaortic innominate vein is an uncommon finding in patients with congenital heart disease. We report a patient with a single ventricle, single atrium, pulmonary atresia, nonconfluent pulmonary artery, persistent left superior caval vein, absent inferior caval vein (azygos connection), right aortic arch, and retroaortic innominate vein. His innominate vein took an … Show more

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Cited by 2 publications
(1 citation statement)
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“…1,18,20 Retroaortic innominate vein has been used for pulmonary artery reconstruction during cavopulmonary anastomosis and right atrial pulmonary anastomosis in a patient with complex cardiac anomalies such as tricuspid atresia/pulmonary atresia, superior-inferior ventricles, and pulmonary atresia with a single ventricle and atrium; therefore, it is important for the surgeon to be aware of its presence. [21][22][23] To conclude, isolated retroaortic innominate vein is an exceedingly rare venous anomaly which has previously not been reported in association with right-sided aortic arch in the absence of cardiac defects. Though usually not of any clinical significance, its presence can present technical difficulties during some cardiac procedures.…”
Section: Discussionmentioning
confidence: 99%
“…1,18,20 Retroaortic innominate vein has been used for pulmonary artery reconstruction during cavopulmonary anastomosis and right atrial pulmonary anastomosis in a patient with complex cardiac anomalies such as tricuspid atresia/pulmonary atresia, superior-inferior ventricles, and pulmonary atresia with a single ventricle and atrium; therefore, it is important for the surgeon to be aware of its presence. [21][22][23] To conclude, isolated retroaortic innominate vein is an exceedingly rare venous anomaly which has previously not been reported in association with right-sided aortic arch in the absence of cardiac defects. Though usually not of any clinical significance, its presence can present technical difficulties during some cardiac procedures.…”
Section: Discussionmentioning
confidence: 99%