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The Journal of Thoracic and Cardiovascular Surgery, Vol 71, 366-370, Copyright © 1976 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
M Yamaguchi, K Horikoshi, A Toriyama, K Kimura and H Mito
Surgical correction was carried out successfully in a severely cyanotic
3-year-old Japanese girl who had a very rare type of double-outlet right
ventricle. The malformation was associated with bilateral conus,
1-transposition of the great arteries, and subpulmonary ventricular septal
defect without significant pulmonary stenosis in situs solitus. A large
amount of subaortic conal musculature which separated the aortic valve from
the subpulmonary ventricular septal defect was removed, as was the anterior
rim of the ventricular septal defect. A tunnel, constructed with a woven
Teflon prosthesis, was inserted in such a manner as to direct blood from
the left ventricle through the defect and out to the aorta. The pulmonary
outflow tract was reconstructed with a Teflon patch lined with pericardium.
The patient's postoperative recovery was uneventful, and she was doing well
3 months postoperatively. To our knowledge, no identical case with a
similar type of surgical correction has previously been reported.
ARTICLES
Successful repair of double-outlet right ventricle with bilateral conus, 1-transposition of great arteries (S,D,L), and subpulmonary ventricular septal defect
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Q. Wu, Q. Yu, and X. Yang Modified Rastelli procedure for double outlet right ventricle with left-malposition of the great arteries: report of 9 cases Ann. Thorac. Surg., January 1, 2003; 75(1): 138 - 142. [Abstract] [Full Text] [PDF] |
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