| Literature DB >> 17908654 |
Huei-Fang Wang1, Chia-Chang Huang, Yu-Fang Chen, Donald Ming-Tak Ho, Hong-Da Lin.
Abstract
Pituitary apoplexy is a rare complication of pituitary tumors. We report a case of a 41-year-old female with acromegaly due to a pituitary macroadenoma, who developed pituitary apoplexy after a thyrotropin-releasing hormone (TRH) 200 microgram intravenous injection stimulation test. Neither emergency computed tomography (CT) scans nor magnetic resonance imaging (MRI), performed 6 hours and 12 hours, respectively, after the active episode, disclosed the evidence of acute hemorrhage or infarction. Two days later, the pituitary mass, removed by transsphenoidal approach, showed ischemic necrosis and acute hemorrhage. The TRH test is generally safe for evaluating pituitary function, but pituitary apoplexy may occur after the procedure. CT and MRI may miss the diagnosis of pituitary apoplexy, especially if performed immediately after the acute episode.Entities:
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Year: 2007 PMID: 17908654 DOI: 10.1016/S1726-4901(08)70026-1
Source DB: PubMed Journal: J Chin Med Assoc ISSN: 1726-4901 Impact factor: 2.743