SOROCABA / SP - quinta-feira, 23 de novembro de 2017

PITUITARY APOPLEXY: ASSOCIATED WITH REMISSION OF ACROMEGALY

Neurosurgery Quarterly:

December 2006 - Volume 16 - Issue 4 - pp 207-209

doi: 10.1097/01.wnq.0000214034.08226.f4

 

Case Reports

 

Pituitary Apoplexy: Associated With Remission of Acromegaly

Uzum, Ayse Kubat MD; Mert, Meral MD; Kutluturk, Faruk MD; Sencer, Altay MD; Goker, Burcu MD; Ozbey, Nese; Aral, Ferihan

 

Abstract

Pituitary apoplexy is defined as an acute, life-threatening infarction of the pituitary gland.

We report a case who presented with diabetic ketoasidosis. After resolution of the acute event, diplopia and partial loss of vision led to diagnosis of a huge sellar mass.

 His physical examination caused us to suspect acromegaly. Transsphenoidal operation was performed. Histopathologic examination of operation material was compatible only with necrosis.

Two months after the acute event, his glucose concentrations were in normal ranges without antidiabetic treatment. Insulinlike growth factor-1 was normal, and after oral glucose load, growth hormone levels were suppressed.

Hypogonadotropic hypogonadism persisted after the operation with no evidence of any other pituitary hormone deficiencies.

Therefore we think that our patient is another example of infarctive apoplexy of a pituitary tumor leading to remission without affecting the pituitary function to a great extent.

 

 

2006 Lippincott Williams & Wilkins, Inc.