Aortico-right ventricular tunnel (ARVT) was successfully corrected in a 32-year-old patient. The diagnosis was preoperatively suspected on the basis of Doppler echocardiography and it was confirmed by a three-dimensional computed tomographic scan. The ARVT originated independently above the right coronary sinus. Surgical closure with 5-0 polypropylene in the middle of the tunnel under modest hypothermia was successfully performed. Follow-up was found to be satisfactory 3 months later.
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http://dx.doi.org/10.1016/j.athoracsur.2009.10.073 | DOI Listing |
J Card Surg
September 2011
Cardiothoracic Center, All India Institute of Medical Sciences, New Delhi, India.
Two patients with aortic right ventricular tunnel and anomalous origin of the right coronary artery from the tunnel are reported. The literature on this condition is reviewed.
View Article and Find Full Text PDFAnn Thorac Surg
June 2010
Department of Cardiovascular Surgery, China-Japan Union Hospital of Jilin University, Changchun, the People's Republic of China.
Aortico-right ventricular tunnel (ARVT) was successfully corrected in a 32-year-old patient. The diagnosis was preoperatively suspected on the basis of Doppler echocardiography and it was confirmed by a three-dimensional computed tomographic scan. The ARVT originated independently above the right coronary sinus.
View Article and Find Full Text PDFFetal Diagn Ther
September 2007
Department of Pediatric Cardiology and Pediatric Cardiac Surgery, Wilhelmina Children's Hospital/University Medical Center, Utrecht, The Netherlands.
In the 36th week of gestation a large aortico-right ventricular tunnel with an otherwise structurally normal heart was diagnosed by fetal echocardiography. This report describes for the first time the impact of the timely prenatal diagnosis of an aortico-right ventricular tunnel followed by successful management in early infancy.
View Article and Find Full Text PDFInt J Cardiol
July 1999
Cardiothoracic Sciences Centre, All India Institute of Medical Sciences, New Delhi.
A 2-year-old child with aortico-right ventricular tunnel is reported for its rarity. The right coronary artery originated from the distal end of the tunnel. The frequent occurrence of coronary artery origin abnormality with this anomaly is highlighted.
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