Pituitary apoplexy most commonly occurs as an acute event with headache, al
tered consciousness, visual deficits, ophthalmoplegia and features of hypop
ituitarism. A 28-year-old man previously well, presented with a 36-hour his
tory of fever, headache and neck stiffness suggestive of meningitis. CSF ex
amination was initially interpreted as a sterile meningitis, but there were
red cells present and xanthochromia consistent with subarachnoid hemorrhag
e, Right sided IIIrd cranial nerve palsy and dense bitemporal hemianopsia d
eveloped 3 days later. A computed tomography of the head with contrast show
ed a ring enhancing suprasellar mass and an MRI demonstrated a large sellar
mass with hemorrhage. Endocrine evaluation, which subsequently became avai
lable, showed evidence of panhypopituitarism, Pituitary apoplexy in a nonse
cretory adenoma was confirmed at transsphenoidal surgical decompression and
by histopathology.