Case report: Pituitary apoplexy presenting as sterile meningitis and subarachnoid hemorrhage

被引:5
|
作者
Bontha, S [1 ]
Hennessey, JV [1 ]
Jackson, IMD [1 ]
机构
[1] Brown Univ, Rhode Isl Hosp, Sch Med, Div Endocrinol, Providence, RI 02903 USA
来源
ENDOCRINOLOGIST | 2000年 / 10卷 / 04期
关键词
D O I
10.1097/00019616-200010040-00010
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Pituitary apoplexy most commonly occurs as an acute event with headache, altered consciousness, visual deficits, ophthalmoplegia and features of hypopituitarism. A 28-year-old man previously well, presented with a 36-hour history of fever, headache and neck stiffness suggestive of meningitis. CSF examination was initially interpreted as a sterile meningitis, but there were red cells present and xanthochromia consistent with subarachnoid hemorrhage, Right sided IIIrd cranial nerve palsy and dense bitemporal hemianopsia developed 3 days later. A computed tomography of the head with contrast showed a ring enhancing suprasellar mass and an MRI demonstrated a large sellar mass with hemorrhage. Endocrine evaluation, which subsequently became available, showed evidence of panhypopituitarism, Pituitary apoplexy in a nonsecretory adenoma was confirmed at transsphenoidal surgical decompression and by histopathology.
引用
收藏
页码:277 / 279
页数:3
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