We describe two cases of giant aneurysm of the LAA that underwent successful treatment at our institute.
Figure 2: Giant aneurysm of left atrial appendage compressing surrounding structures.
Figure 3: Excision of left atrial appendage aneurysm.
Case 2– A 48-year-old male presented with dyspnea on exertion NYHA class 2, palpitation, and giddiness. A physical examination revealed an irregularly irregular pulse. An electrocardiogram showed atrial fibrillation with a fast ventricular rate, and a chest X-ray revealed a prominent bulge at the left heart border. A transthoracic echocardiogram showed an LAA aneurysm extending posterosuperiorly which was lateral to the pulmonary artery with a layered clot in it and trivial MR. Transesophageal echocardiography revealed an LAA aneurysm of 7.5x5.3 cm, posterior inferior lateral to the left ventricle (LV), showing dense contrast and a small clot at the apex. Cardiac catheterization showed MPA pressure of 23/11 mmHg, and a pulmonary arteriogram in levo phase revealed opacification of the LA and LAA aneurysm. A contrast-enhanced, spiral CT scan showed an LAA aneurysm measuring 9.5x8.7x5.8 cm with no evidence of thrombus or calcification. In view of the doubtful clot in the aneurysm, the procedure was performed through median sternotomy and CPB using cold blood cardioplegia. Intraoperative findings were a giant LAA aneurysm measuring 15x7x7 cm with a 5 cm neck and the absence of a clot with a normal mitral valve. The LAA aneurysm was excised, and the edges were approximated with a 4-0 polypropylene suture in two layers. Weaning from the CPB was achieved in sinus rhythm. On immediate postoperative, three-month, and one-year follow-up, the patient was asymptomatic, and his electrocardiogram and two-dimensional echocardiography showed normal sinus rhythm and mild mitral regurgitation with good biventricular function. A histopathological examination revealed an irregularly thickened myocardium with the overlying epicardium being comprised of fibroelastic tissue lined by mesothelial cells with extensive fibrosis.
Declaration of conflicting interests
The authors declared no conflicts of interest with respect
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