Korean J Thorac Cardiovasc Surg.
1999 Sep;32(9):827-830.
Congenital Left Atrial Appendage Aneurysm: A Case Report
- Affiliations
-
- 1Department of Thoracic and Cardiovascular Surgery, School of Medicine,
Kyungpook National University. ktkim@kyungpook.ac.kr
Abstract
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Congenital left atrial appendage aneurysm is a very rare congenital cardiac abnormality.
That is postulated to arise from a developmental weakness in the atrial wall in utero.
Clinically, patients are often asymptomatic and are diagnosed incidentally, but
supraventricular arrhythmias and systemic thromboembolism have also been reported
in some cases. Surgical resection at the time of diagnosis is recommended because of the
propensity for thromboembolic complications. A 13-month-old female, who was suspected
preoperatively as having partial absence of pericardium with left atrial herniation through
the defect, underwent surgical resection of the left atrial appendage aneurysm. Exposure
through a median sternotomy showed an intact pericardium. The postoperative course was
uneventful.