Pituitary Apoplexy

被引:72
作者
Briet, Claire [1 ,2 ]
Salenave, Sylvie [1 ]
Chanson, Philippe [1 ,2 ,3 ]
机构
[1] Hop Bicetre, AP HP, Dept Endocrinol & Reprod Dis, F-94725 Le Kremlin Bicetre, France
[2] Univ Paris 11, Sch Med, F-91405 Orsay, France
[3] Inst Natl Sante & Rech Med, Unit 693, F-94726 Le Kremlin Bicetre, France
关键词
Pituitary apoplexy; Emergency; Neurosurgery; Magnetic resonance imaging; Hemorrhage; Necrosis; Pituitary adenoma; Corticotropic deficiency; TUMOR APOPLEXY; CONSERVATIVE MANAGEMENT; PRECIPITATING FACTORS; CLINICAL-FEATURES; ADENOMAS; OUTCOMES; SURGERY; MRI; UK;
D O I
10.1016/j.ecl.2014.10.016
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Pituitary apoplexy (PA) is a rare clinical syndrome caused by sudden hemorrhaging and/or infarction of the pituitary gland, generally within a pituitary adenoma. The main symptom is sudden-onset severe headache, associated with visual disorders or ocular palsy. Corticotropic deficiency may be life-threatening if left untreated. Computed tomography (CT) or MRI confirms the diagnosis by revealing a pituitary tumor with hemorrhagic and/ or necrotic components. PA used to be considered a neurosurgical emergency but a conservative approach is increasingly used in selected patients, as it yields similar outcomes. Glucocorticoid treatment must always be started immediately after onset.
引用
收藏
页码:199 / +
页数:13
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