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A rare giant congenital left atrial appendage aneurysm in a 1‐day‐old newborn
Congenital left atrial appendage aneurysm (LAAA) is a very rare condition and occurs as a result of congenital dysplasia of musculi pectinate. These patients may be asymptomatic and/or may present with dyspnea, and thromboembolic events. The most common complications are life‐threatening thromboembo...
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Published in: | Echocardiography (Mount Kisco, N.Y.) N.Y.), 2018-05, Vol.35 (5), p.757-759 |
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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: | Congenital left atrial appendage aneurysm (LAAA) is a very rare condition and occurs as a result of congenital dysplasia of musculi pectinate. These patients may be asymptomatic and/or may present with dyspnea, and thromboembolic events. The most common complications are life‐threatening thromboembolic events and supraventricular tachyarrhythmias. Transthoracic echocardiography plays a very important role in the diagnosis of LAAA. Herein, we present a rare case of giant congenital LAAA. |
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ISSN: | 0742-2822 1540-8175 |
DOI: | 10.1111/echo.13883 |