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Interact CardioVasc Thorac Surg 2008;7:1180-1182. doi:10.1510/icvts.2007.174367
© 2008 European Association of Cardio-Thoracic Surgery

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Case report - 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 Nagashimaa,*, Narutoshi Hibinoa, Eiichi Yamamotob and Takashi Higakic

a Department of Cardiovascular Surgery, Ehime Prefectural Central Hospital, 83 Kasuga-cho, Matsuyama-city, Ehime, 790-0024 Japan
b Department of Pediatrics, Ehime Prefectural Central Hospital, Ehime, Japan
c Department of Pediatrics, Ehime University of Medicine, Ehime, Japan

Corresponding author. Tel.: +81-89-947-1111 ext. 2250; fax: +81-89-943-4136.

E-mail address: mitsugi{at}aqua.plala.or.jp (M. Nagashima).

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 artesian 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.

Key Words: Pulmonary abnormal arborization; Single ventricle; Staged Fontan operation







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