2Department of Echocardiography, Wuhan Asia Heart Hospital Affiliated to Wuhan University of Science and Technology, Wuhan, P.R. China
CONTENT
A 62-year-old woman presented with chest tightness and discomfort for 2 years. Physical examination and laboratory tests were unremarkable. Transthoracic echocardiography revealed dilatation of the ascending aorta and mild aortic regurgitation. Maximum intensity projection computed tomography angiography (CTA) showed that a levoatrial cardinal vein (LACV) connected the anterior wall of the left atrium (LA) to the right atrium (RA) (
Levoatrial cardinal vein is an anomalous connection between the LA or pulmonary vein and the systemic vein.1 It generally originates from the pulmonary vein or the LA and drains into the superior vena cava or the innominate vein. It can be associated with hypoplastic left heart syndrome (HLHS), tetralogy of Fallot, mitral or aortic atresia, or aortic stenosis, as well as cor triatriatum.2 The LACV with an interatrial communication is extremely rare.3 Although rare, the ability to identify LACV is clinically significant because it may result in a bidirectional shunt, and the development of symptoms is an indication for intervention. It is essential to recognize this embryologic abnormality and report it in patients who require surgical ligation or transcatheter closure.4 Computed tomography angiography is an effective method for determining the anatomy of complex heart abnormalities. It can distinguish between LACV and persistent left superior vena cava, vertical vein of partial anomalous pulmonary venous connection, left superior intercostal vein, and veno-venous bridges.5
Footnotes
References
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