Giant congenital diverticulum of the right atrium
Munesh Tomar1, Sitaraman Radhakrishnan, Krishna Subramony Iyer
1Department of Pediatric & Congenital Heart Diseases, Escorts Heart Institute & Research Centre, New Delhi, India. muneshtomar@yahoo.com
Insights
A rare congenital heart condition, right atrial diverticulum, was successfully treated in a 3-year-old child. Surgical excision resolved symptoms of early fatigability, highlighting effective management for this uncommon cardiac anomaly.
Area of Science:
- Cardiology
- Pediatric Surgery
- Congenital Heart Disease
Background:
- Congenital diverticulum of the heart is a rare condition that can affect various heart chambers.
- Symptoms may include early fatigability, particularly in pediatric patients.
- Accurate diagnosis often requires advanced imaging techniques.
Observation:
- A 3-year-old child presented with a 6-month history of early fatigability and recent upper respiratory infection.
- Chest X-ray and echocardiogram indicated significant right atrial enlargement.
- Surgical intervention was performed to address the congenital heart anomaly.
Findings:
- A right atrial diverticulum was identified and surgically excised under cardiopulmonary bypass.
- Pathological examination revealed thickened endocardium with edema and myocardial fiber hypertrophy.
- The patient's symptoms of early fatigability were resolved post-surgery.
Implications:
- This case demonstrates the successful surgical management of a rare congenital right atrial diverticulum in a child.
- Early diagnosis and intervention are crucial for improving outcomes in pediatric congenital heart diseases.
- Further research into congenital heart diverticula can enhance understanding and treatment strategies.
Abstract:
Congenital diverticulum of heart is a rare entity, which may arise from the atria, atrial appendages, coronary sinus or the ventricles. A 3-year-old child presented with history of early fatigability for 6 months and recent upper respiratory tract infection. Chest X-ray and echocardiogram revealed marked right atrial enlargement. At surgery, a right atrial diverticulum was excised under cardiopulmonary bypass. Pathology revealed thickened endocardium with edema and myocardial fiber hypertrophy. Our experience with this rare congenital disease is presented along with a review of the literature.
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