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- S Tokunaga, H Kado, Y Imoto, Y Shiokawa, and H Yasui.
- Department of Cardiovascular Surgery, Fukuoka Children's Hospital, Japan.
- Ann. Thorac. Surg. 2001 Feb 1; 71 (2): 715-7.
AbstractEctopia cordis is a very rare and often fatal disease. We report a successful surgery case of thoracoabdominal ectopia cordis with univentricular heart. This patient underwent a three-stage Fontan procedure, a right-modified Blalock-Taussig shunt at the age of 1 month, bidirectional Glenn shunt and pulmonary arterioplasty at 2 years 8 months, and finally a total cavopulmonary connection at 4 years. This patient was discharged from the hospital in good condition and has been doing well since. Thus, ectopia cordis is not a contraindication for a Fontan operation.
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