Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2875439 | The Annals of Thoracic Surgery | 2013 | 4 Pages |
Abstract
Pheochromocytomas are catecholamine-producing paragangliomas derived from the neural crest. Primary cardiac pheochromocytoma is extremely rare. We describe a case of cardiac pheochromocytoma involving both right and left atria in a middle-aged woman. Metaiodobenzylguanidine (MIBG) scintiscan results were normal, but results from an octreotide scan were abnormal. The tumor was successfully resected using cardiopulmonary bypass (CPB).
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Authors
Xingrong MD, Qi MD, Heng MD, Chaoji MD, Lihua MD, Guotao MD, Zhengpei MD,