Bm. Arafah et al., PITUITARY-TUMOR APOPLEXY - PATHOPHYSIOLOGY, CLINICAL MANIFESTATIONS, AND MANAGEMENT, Journal of intensive care medicine, 12(3), 1997, pp. 123-134
Pituitary tumor apoplexy represents a rare clinical syndrome caused by
hemorrhagic infarction of an existing, often previously unrecognized,
large adenoma. We present our approach and experience in the field, a
nd we provide a summary of pertinent published literature addressing d
iagnosis, management, and pathophysiology of the clinical manifestatio
ns of pituitary tumor apoplexy. Although many precipitating factors ar
e known, most episodes occur spontaneously and present clinically with
relatively sudden onset of severe headache, visual field defects, and
ophthalmoplegia. Either computed tomography (nonenhanced and enhanced
) or magnetic resonance imaging in a symptomatic patient can define pe
rtinent anatomical changes and aid in establishing diagnosis. Immediat
e treatment with corticosteroids is necessary. Patients with the mild
form of the syndrome respond quickly to steroids and can be managed co
nservatively with continued glucocorticoid therapy Most patients with
persistent neural deficits require urgent trans-sphenoidal decompressi
on. Unless surgery is delayed, results of transsphenoidal decompressio
n are usually very good, and improvements in neurological symptoms and
endocrine function are noted within hours to daps of the procedure. P
atients need to be closely followed up after the episode because a lar
ge number continue to have residual tumor requiring additional therapy
, or they have pituitary hormone abnormalities that need treatment. Cl
ose interaction between neurosurgeons and endocrinologists in the mana
gement of patients with pituitary tumor apoplexy is essential for opti
mal outcome.