Paragangliomas (glomus tumors) comprise 15% of all neoplasms at the sk
ull base. Despite extensive growth, these tumors usually do not secret
e active biogenic substances into the circulation in sufficient quanti
ties to produce symptoms. When they do secrete large amounts of catech
olamines, they will cause symptoms that mimic a pheochromocytoma. The
still confusing nomenclature of paragangliomas is reviewed, and the cl
inical work-up, surgical treatment, and follow-up of five patients wit
h catecholamine-secreting paragangliomas of temporal bone (3), infrate
mporal fossa (1), and nasopharynx (1) are presented and discussed.