Cardiac pheochromocytoma is an exceedingly rare and unusual clinical entity
. Only 37 previous surgically treated adult patients were found in review o
f the surgical literature. We report the case of a 13-year-old boy who had
a cardiac pheochromocytoma that was localized by the Ill-indium diethylenet
riamine pentaacetic acid octreotide scintigraphy scan and confirmed by magn
etic resonance imaging after computed tomographic and B1-iodine-metaiodoben
zylguanidine scans had failed. At operation, a 6-cm pheochromocytoma of the
left atrium was found and successfully resected with reconstruction of the
left atrium using autologous pericardium. (C) 1999 by The Society of Thora
cic Surgeons.