Ooi T C, Holdaway I M, Donald R A, Ibbertson H K
J Endocrinol Invest. 1980 Jan-Mar;3(1):45-9. doi: 10.1007/BF03348216.
A 28 year old woman presented with symptoms and biochemical findings suggesting hypoglycemia. Detailed endocrine investigations indicated secondary adrenocortical insufficiency with no rise in plasma ACTH or plasma cortisol following insulin-induced hypoglycemia or vasopressin infusion. The adrenal glands however produced cortisol normally following prolonged stimulation with depot tetracosactrin. Other anterior pituitary hormones were released normally following appropriate stimulation tests. The literature on isolated ACTH deficiency is briefly reviewed, and this case represents one of the few reports in which the diagnosis has been substantiated by ACTH radioimmunoassays.
一名28岁女性出现提示低血糖的症状和生化检查结果。详细的内分泌检查表明存在继发性肾上腺皮质功能不全,胰岛素诱发低血糖或输注血管加压素后血浆促肾上腺皮质激素(ACTH)及血浆皮质醇均未升高。然而,长效四肽促肾上腺皮质激素长时间刺激后,肾上腺能正常分泌皮质醇。适当的刺激试验后,其他垂体前叶激素正常释放。本文简要回顾了关于孤立性ACTH缺乏症的文献,该病例是少数通过ACTH放射免疫测定得以确诊的报告之一。