Surgically Treated Giant Right Atrium in Isolated Severe Tricuspid Regurgitation

Severe tricuspid regurgitation (TR) can lead to significant enlargement of the right atrium (RA) and poses unique clinical challenges. We report this case of a 17-year-old boy previously misdiagnosed with Ebstein anomaly who presented with dyspnea and palpitations. Initial examination revealed irregular heart rhythm, distended neck veins, and a significant murmur. Echocardiogram and computed tomography showed severe TR due to noncoaptation of the tricuspid valve, causing massive RA enlargement (1916 mL). The patient underwent successful surgical intervention, including tricuspid valve replacement and RA reduction. Postoperative complications included atrial fibrillation, which was medically managed. To our knowledge, this case had the largest RA to be reported and surgically treated in the literature. The case underscores the diagnostic challenges in differentiating severe TR from Ebstein anomaly and the progression from TR to significant RA enlargement. Accurate diagnosis and timely surgical management are critical in such cases to achieve favorable outcomes.

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Publication Details

Journal
World Journal for Pediatric and Congenital Heart Surgery
Published
2025-09-09
DOI
https://doi.org/10.1177/21501351251365532
Primary Topic
Cardiac Valve Diseases and Treatments
Type
article
Field-Weighted Citation Impact
0.00
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article

Surgically Treated Giant Right Atrium in Isolated Severe Tricuspid Regurgitation

Raisa Bano, Sohail Khan Bangash, Rizwan Ali, Waqar Ahmad Khan et al.
World Journal for Pediatric and Congenital Heart Surgery
Cardiac Valve Diseases and Treatments
article

Surgically Treated Giant Right Atrium in Isolated Severe Tricuspid Regurgitation

Raisa Bano, Sohail Khan Bangash, Rizwan Ali, Waqar Ahmad Khan, Maria Syed
article en

Abstract

Severe tricuspid regurgitation (TR) can lead to significant enlargement of the right atrium (RA) and poses unique clinical challenges. We report this case of a 17-year-old boy previously misdiagnosed with Ebstein anomaly who presented with dyspnea and palpitations. Initial examination revealed irregular heart rhythm, distended neck veins, and a significant murmur. Echocardiogram and computed tomography showed severe TR due to noncoaptation of the tricuspid valve, causing massive RA enlargement (1916 mL). The patient underwent successful surgical intervention, including tricuspid valve replacement and RA reduction. Postoperative complications included atrial fibrillation, which was medically managed. To our knowledge, this case had the largest RA to be reported and surgically treated in the literature. The case underscores the diagnostic challenges in differentiating severe TR from Ebstein anomaly and the progression from TR to significant RA enlargement. Accurate diagnosis and timely surgical management are critical in such cases to achieve favorable outcomes.

World Journal for Pediatric and Congenital Heart SurgeryVol. 17(1)
National Institute of Cardiovascular Diseases (PK)
Openalex Percentile: Top 63%
Cardiac Valve Diseases and Treatments
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