scholarly journals Surgical Repair of Ventricular Septal Defect Associated with Congenitally Corrected Transposition of the Great Arteries.

1991 ◽  
Vol 20 (7) ◽  
pp. 1259-1263
Author(s):  
Ryo AEBA ◽  
Shigeyuki TAKEUCHI ◽  
Hiroji IMAMURA ◽  
Hankei SHIN ◽  
Yoshiyuki HAGA ◽  
...  
Author(s):  
Kévin Gardey ◽  
Rémi Thevenard ◽  
Hervé Joly ◽  
Francis Bessière

Abstract Background Twin atrio ventricular (AV) nodal tachycardia is a rare mechanism of supra ventricular arrhythmia, only seen in some specific congenital heart defects (CHD). It consists of a reentrant circuit between two distinct AV nodes (anterior and inferior). Since both nodes have antegrade and retrograde conduction, there is usually two QRS morphologies in sinus rhythm. Case summary This case is about an atypical twin AV nodal tachycardia in a 15 years-old patient with congenitally corrected transposition of the great arteries (cc-TGA) and previous history of a ventricular septal defect (VSD) repair. The surgical closure was probably responsible of a poor antegrade conduction over the inferior AV node, that was responsible for a unique QRS morphology. He finally received a catheter ablation of the inferior AV node. He remained asymptomatic without anti-arrhythmic drugs at 8-months post-ablation. Discussion Twin atrioventricular nodal re-entrant tachycardia is a rare phenomenon. The presentation and electrophysiological study can be both atypical due to previous surgical repair. Operator should be aware of specific CHD where twin atrioventricular nodal re-entrant tachycardias are expected.


1994 ◽  
Vol 4 (2) ◽  
pp. 175-177 ◽  
Author(s):  
Vicki Knight-Mathis ◽  
Carol M. Cottrill ◽  
Robert K. Salley

SummaryAccessory atrioventricular valvar tissue is uncommon and, on occasion, has been identified as a cause of ventricular outflow obstruction. Accessory tricuspid valvar tissue has been reported to cause subpulmonary obstruction but infrequently has accessory tissue arising from the mitral valve been associated with obstruction. This paper reports two cases of subvalvar obstruction; the first in association with a ventricular septal defect causing subaortic obstruction and the other in association with congenitally corrected transposition and a ventricular septal defect, causing subpulmonary obstruction.


1999 ◽  
Vol 9 (2) ◽  
pp. 207-209 ◽  
Author(s):  
Martial M. Massin ◽  
Götz von Bernuth

AbstractWe describe an infant with congenitally corrected transposition, ventricular septal defect and severe pulmonary stenosis. The heart occupied a midline position. Extension of ductal tissue had resulted in occlusion of the left pulmonary artery. As far as we are aware, this is the first report of an association of coarctation of the left pulmonary artery with corrected transposition.


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