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分泌皮质酮的肾上腺皮质癌与空蝶鞍综合征:一例报告

Corticosterone secreting adrenal carcinoma and empty sella turcica: a case report.

作者信息

Krølner B, Larsen S, Nielsen M D

出版信息

Acta Endocrinol (Copenh). 1979 Aug;91(4):650-6. doi: 10.1530/acta.0.0910650.

Abstract

Pituitary adenoma was suspected in a woman of 74 with hypercorticism,hypokalaemic alkalosis and radiographically enlarged sella turcica. However, non-suppressibility of steroid excretion by high-dose dexamethasone and low plasma concentration of ACTH suggested adrenal tumour. Detailed analysis of urinary steroid excretions demonstrated unusually large amounts of corticosterone metabolites, 14.6 mg/24 h compared to a mean normal value of 0.5 mg. The basal levels of the remaining pituitary hormones were unremarkable. The patient died incidentally before a planned adrenalectomy. The autopsy disclosed an adrenal carcinoma and an empty sella turcica. The enlarged pituitary fossa was lined by a narrow rim of histological normal pituitary tissue.

摘要

一名74岁女性,有皮质醇增多症、低钾性碱中毒且影像学显示蝶鞍增大,怀疑患有垂体腺瘤。然而,高剂量地塞米松不能抑制类固醇排泄以及促肾上腺皮质激素血浆浓度低提示肾上腺肿瘤。对尿类固醇排泄的详细分析显示皮质酮代谢产物量异常大,为14.6毫克/24小时,而正常平均值为0.5毫克。其余垂体激素的基础水平无异常。该患者在计划的肾上腺切除术之前意外死亡。尸检发现肾上腺癌和空蝶鞍。扩大的垂体窝内衬有组织学正常的垂体组织窄边。

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