Department of Neurosurgery, Eberhard-Karls-University Hospital Tübingen, Tübingen, Germany.
Neurol Sci. 2010 Apr;31(2):217-8. doi: 10.1007/s10072-009-0210-z. Epub 2010 Jan 30.
The rare case of a patient with SIADH following pituitary adenoma apoplexy is reported. Since apoplexy did not exert any mass effect on surrounding structures, the patient was treated conservatively and the anterior pituitary gland insufficiency has been substituted adequately. Seven days after the apoplexy the patient again showed low serum-Na(+) levels despite cortisol substitution. Diagnosis of SIADH was made. It is essential to be aware of this rare syndrome in patients with pituitary adenoma apoplexy.
报告了一例垂体腺瘤卒中后抗利尿激素分泌不当综合征(SIADH)的罕见病例。由于卒中未对周围结构产生任何占位效应,因此患者接受了保守治疗,且垂体前叶功能减退已得到充分替代。卒中后 7 天,尽管已进行皮质醇替代治疗,但患者的血清钠(Na+)水平再次降低。诊断为 SIADH。对于垂体腺瘤卒中患者,了解这种罕见综合征至关重要。