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Published on September 3, 2008
Interactive CardioVascular and Thoracic Surgery 2008, doi:10.1510/icvts.2007.174367
© 2008 European Association of Cardio-Thoracic Surgery

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Mitsugi Nagashima
Narutoshi Hibino
Eiichi Yamamoto
Takashi Higaki
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Right arrow Congenital - cyanotic

Congenital

Total cavopulmonary connection for functionally single ventricle with pulmonary atresia and abnormal arborization of pulmonary arteries - exclusion of overwhelmed area by collateral arteries from Fontan circulation

Mitsugi Nagashima 1*, Narutoshi Hibino 1, Eiichi Yamamoto 1, Takashi Higaki 2

1 Ehime Prefectural Central Hospital, Japan
2 Ehime University of Medicine, Japan

* To whom correspondence should be addressed. E-mail: mitsugi{at}aqua.plala.or.jp.


   Abstract
Functionally single ventricle with major aortopulmonary collateral arteries and pulmonary atresia is very rare. Surgical indication for this combination of abnormalities is still unclear and Fontan procedure is still a crucial challenge for the patient who has this anomaly. We report a case with asplenia, functionally single ventricle, pulmonary atresia and pulmonary abnormal arborization who successfully underwent staged Fontan operation. In this case, the left upper lobe area, where the flow from a Glenn shunt was overwhelmed by the collateral arterial blood flow, was excluded from the Fontan circulation by the ligation of the left upper pulmonary arterial branch at its most proximal side at the time of fenestrated extracardiac total cavopulmonary connection. Keywords: Pulmonary abnormal arborization; Single ventricle; Staged Fontan operation





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