Background: The wide availability of computed tomography and magnetic
resonance imaging has resulted in the discovery of unsuspected endocri
nologically silent pituitary masses (incidentalomas). Because the natu
ral history of this entity is not known, the approach to the pituitary
incidentaloma has not been established. Objective: To determine the n
atural history of untreated pituitary incidentaloma, recognizing that
this includes lesions of various causes. Methods: Thirty-one adults wi
th incidentalomas were prospectively followed up conservatively for a
mean of 6.4 years (range, 3 to 11 years). Clinical and biochemical ass
essment, computed tomography or magnetic resonance imaging of the pitu
itary, and visual field testing by Goldmann perimetry at baseline, 6 m
onths, and yearly thereafter were the outcomes assessed. Results: Only
patients with pituitary incidentalomas greater than 10 mm in greatest
diameter developed tumor enlargement or complications. Three patients
developed asymptomatic tumor enlargement. In four patients, masses de
creased in size. Only two patients developed complications. One requir
ed subsequent surgery. The only permanent impairment was panhypopituit
arism following surgery in this patient. Conclusions: Patients with pi
tuitary incidentalomas of unknown causes usually follow a benign cours
e for at least 6 years after discovery. Neurosurgical intervention is
not initially required in the management of pituitary incidentalomas,
particularly those less than 10 mm, as long as clinical observation ca
n be continued.