Ebstein malformation of tricuspid valve
Malformação de Ebstein da valva tricúspide
CategoryDefinition
Ebstein's anomaly is a malformation of the tricuspid valve and right ventricle that is characterized by a spectrum of several features: (1) incomplete delamination of septal and inferior (posteror) tricuspid valve leaflets from the myocardium of the right ventricle; (2) downward (apical) displacement of the functional annulus; (3) dilation of the "atrialized" portion of the right ventricle with variable degrees of hypertrophy and thinning of the wall; (4) redundancy, fenestrations, and tethering of the anterosuperior leaflet; and (5) dilation of the right atrioventricular junction (the true tricuspid annulus). These anatomical and functional abnormalities cause tricuspid regurgitation (and rarely tricuspid stenosis) that results in right atrial and right ventricular dilatation and atrial and ventricular arrhythmias. Associated cardiac anomalies include an interatrial communication, the presence of accessory conduction pathways and dilation of the right atrium and right ventricle. Varying degrees of right ventricular outflow tract obstruction may be present, including pulmonary atresia. Some patients with discordant atrioventricular and ventriculoarterial connections [congenitally corrected transposition] have an Ebstein-like deformity of the left-sided morphologically tricuspid valve.