A Rare Intracardiac Mass: Cardiac Paraganglioma
It is very rare for heart tissue to give rise to a primary paraganglioma. Here, we report the observation of such a tumour in a 34-year-old woman who presented with symptoms of pulmonary venous congestion. The findings from echocardiography were consistent with the diagnosis of a myxoma that was partially occluding the left atrium. Surgery was performed in which a large (6
cm
×
5
cm
×
3
cm), non-lobulated solid tumour was resected from the posterior wall of the atrium. Upon histologic evaluation, this was determined to be a cardiac paraganglioma.
Keywords: Cardiac tumours, Paraganglioma
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PII: S1443-9506(06)00291-5
doi:10.1016/j.hlc.2006.12.002
© 2006 Australasian Society of Cardiac and Thoracic Surgeons and the Cardiac Society of Australia and New Zealand. Published by Elsevier Inc. All rights reserved.
