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Right Atrial Appendage Aneurysm: A Systematic Review
Background Right atrial appendage aneurysm (RAAA) is rare with fewer than 20 cases reported in the literature. We sought to systematically review the published cases of RAAA in terms of demographics, clinical characteristics, treatment, complications, and outcome. Methodology Electronic search for c...
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Published in: | Echocardiography (Mount Kisco, N.Y.) N.Y.), 2014-04, Vol.31 (4), p.534-539 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Background
Right atrial appendage aneurysm (RAAA) is rare with fewer than 20 cases reported in the literature. We sought to systematically review the published cases of RAAA in terms of demographics, clinical characteristics, treatment, complications, and outcome.
Methodology
Electronic search for case reports, case series, and related articles published until July 2013 was carried out and clinical data were extracted and analyzed.
Results
Seventeen cases of RAAA were identified with equal sex distribution and commonly presenting in the third decades of life. Dyspnea and palpitation were the most common clinical presentations. Echocardiography was the most common diagnostic modality. The mean size of aneurysm was 8.83 ± 4.84 × 6.05 ± 2.99 cm. Most of the patients were treated medically with close follow‐up. The mean follow‐up period was 10 months. Atrial tachyarrhythmias and heart failure were the most common complications.
Conclusion
Right atrial appendage aneurysm although rare may be associated with significant morbidity. Surgical resection is indicated in symptomatic patients. |
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ISSN: | 0742-2822 1540-8175 |
DOI: | 10.1111/echo.12510 |