Abstract
This report documents 2 patients who presented with cyanosis early in life. In both instances the necropsy showed the simultaneous occurrence of an imcomplete type of persistent atrioventricular canal and an Ebstein's malformation of the "tricuspid" valve component. In the first patient no clinical investigations were done. In the second patient the electrocardiogram was consistent with persistent atrioventricular canal and the angiocardiogram showed the characteristic goose-neck deformity. Moreover, an abnormality of the right cardiac contour was seen, which in retrospect was correlated with the right-sided Ebstein's malformation. Ebstein's anomaly may significantly alter the clinical and haemodynamic profile of atrioventricular canal and should be considered in atypical cases. The presence of Ebstein's anomaly will complicate surgical repair of the atrioventricular canal.
Full text
PDF




Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- BURCHELL H. B., DUSHANE J. W., KILBY R. A., WOOD E. H. Ebstein's malformation: a clinical and laboratory study. Medicine (Baltimore) 1956 Sep;35(3):161–185. [PubMed] [Google Scholar]
- LEV M., AGUSTSSON M. H., ARCILLA R. The pathologic anatomy of common atrioventricular orifice associated with tetralogy of Fallot. Am J Clin Pathol. 1961 Nov;36:408–416. doi: 10.1093/ajcp/36.5.408. [DOI] [PubMed] [Google Scholar]




