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Giant right atrial aneurysm: a case report
Insights
Giant right atrial aneurysm, a rare congenital heart defect, can be diagnosed before birth. Surgical repair in infancy is recommended to prevent future complications like arrhythmias.
Area of Science:
- Cardiology
- Pediatric Surgery
- Congenital Heart Disease
Background:
- Giant right atrial aneurysm is an exceedingly rare congenital cardiac anomaly.
- Diagnosis during the fetal period presents unique management challenges.
Observation:
- A case of giant right atrial aneurysm diagnosed prenatally is presented.
- The infant underwent surgical intervention at four months of age.
Findings:
- Surgical management involved excision of the aneurysmal portion.
- Repair was completed using a pericardial patch graft.
Implications:
- Early surgical repair is crucial for preventing long-term sequelae.
- Potential complications include arrhythmias and thromboembolic events, underscoring the need for timely intervention.
Abstract:
Giant right atrial aneurysm is a very rare congenital heart defect. We report a case which was diagnosed during fetal life and operated on at 4 months of age with excision of the aneurysmal part and pericardial patch closure. Early repair is recommended to prevent late complications such as arrhythmias and thromboembolic phenomena.
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