Ebstein’s Anomaly and Echocardiographic Features

Aim: To present the various echocardiographic spectrum of Ebstein’s malformation in adolescence and adults. Introduction: Ebstein’s anomaly has different anatomic and hemodynamic variables with clinical manifestations of cyanosis, right-sided heart failure and arrhythmias. The leaflet tethering and dysplasia, together with dilatation of the tricuspid valve ring, constitute the anatomic cause of tricuspid regurgitation observed in this condition. Case reports: The spectrum of leaflet tethering from mild to extreme with varying degrees of tricuspid regurgitation were documented by echocardiography in a 16-year-old cyanotic male with Ebstein’s anomaly associated with an atrial septal defect and mild low tricuspid regurgitation (TR), 22-year-old acyanotic male with right-sided heart failure due to severe tricuspid regurgitation and an intact atrial septum, 55-year-old aymptomatic female with moderate high tricuspid regurgitation. The extreme form was described as an ‘atretic’ membrane in a 28-year-old cyanotic male and as a ‘blanket’ of leaflet tissue in a 30-year-old cyanotic male. Conclusion: Ebstein’s anomaly has to be suspected clinically in presence of cyanosis with a WPW (Wolf-Parkinson-White) or atrioventricular (AV) block pattern of ECG and its management is complex and must be individualized. RV (right ventricular) exclusion procedures are preferred in advanced cases.

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Publication Details

Journal
International journal of cardiovascular medicine.
Published
2024-10-11
DOI
https://doi.org/10.31579/2834-796x/074
Primary Topic
Congenital Heart Disease Studies
Type
article
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article

Ebstein’s Anomaly and Echocardiographic Features

Ramachandran Muthiah
International journal of cardiovascular medicine.
Congenital Heart Disease Studies
article

Ebstein’s Anomaly and Echocardiographic Features

Ramachandran Muthiah
article en

Abstract

Aim: To present the various echocardiographic spectrum of Ebstein’s malformation in adolescence and adults. Introduction: Ebstein’s anomaly has different anatomic and hemodynamic variables with clinical manifestations of cyanosis, right-sided heart failure and arrhythmias. The leaflet tethering and dysplasia, together with dilatation of the tricuspid valve ring, constitute the anatomic cause of tricuspid regurgitation observed in this condition. Case reports: The spectrum of leaflet tethering from mild to extreme with varying degrees of tricuspid regurgitation were documented by echocardiography in a 16-year-old cyanotic male with Ebstein’s anomaly associated with an atrial septal defect and mild low tricuspid regurgitation (TR), 22-year-old acyanotic male with right-sided heart failure due to severe tricuspid regurgitation and an intact atrial septum, 55-year-old aymptomatic female with moderate high tricuspid regurgitation. The extreme form was described as an ‘atretic’ membrane in a 28-year-old cyanotic male and as a ‘blanket’ of leaflet tissue in a 30-year-old cyanotic male. Conclusion: Ebstein’s anomaly has to be suspected clinically in presence of cyanosis with a WPW (Wolf-Parkinson-White) or atrioventricular (AV) block pattern of ECG and its management is complex and must be individualized. RV (right ventricular) exclusion procedures are preferred in advanced cases.

International journal of cardiovascular medicine.Vol. 3(5)
Openalex Percentile: Top 71%
Congenital Heart Disease Studies
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