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Giant Right Atrial Aneurysm in an Infant
Swati Garekar1, Ronak Sheth1, Nitin Chaubal2
1Department of Pediatric Cardiology, 425959Fortis Pediatric and Congenital Heart Centre, Mulund, Mumbai, MH, India.
A rare congenital heart defect, giant right atrial aneurysm (RAA) was detected before birth. Surgical removal successfully treated the infant, preventing further thrombo-embolic events.
Area of Science:
- Cardiology
- Congenital Heart Disease
- Pediatric Surgery
Background:
- Right atrial aneurysm (RAA) is a rare congenital anomaly.
- Clinical presentation of RAA is diverse.
- Antenatal detection of RAA is uncommon.
Observation:
- A case of a giant RAA detected antenatally is presented.
- The infant experienced staring spells, suspected to be thrombo-embolic events from the RAA.
- The right coronary artery was displaced due to RAA invagination.
Findings:
- Successful surgical resection of the giant RAA was performed.
- The right coronary artery was preserved during surgery.
- The anatomical relationship between RAA and the coronary artery was noted.
Implications:
- This case highlights the importance of antenatal diagnosis of RAA.
- Successful surgical management can prevent serious complications like thrombo-embolism.
- Understanding the anatomical variations associated with RAA is crucial for surgical planning.
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