Recurrent pituitary tumors can sometimes pose a diagnostic and therape
utic challenge. We report a case of a 43-year-old man who presented tw
ice, 13 years apart, with pituitary adenoma marked by headaches, visua
l impairment, and no signs of endocrinologic abnormality. At initial p
resentation computed tomographic scan documented a pituitary mass erod
ing the sellar floor, with suprasellar and parasellar extension. The p
atient underwent transsphenoidal surgery and the tumor was classified
as a silent corticotroph adenoma, subtype 2. Thirteen years later, cli
nical symptoms of a destructive pituitary mass reappeared. This time,
the adenoma revealed typical ultrastructural features of an oncocytoma
; it had a different immunocytochemical profile from the first turner,
Given these striking morphologic differences, we consider the two ade
nomas to represent asynchronous, de novo formations. We conclude that
the recurrence of a resected pituitary tumor may also represent a meta
chronous development of two distinct pituitary adenomas.