Páv J, Srámková J, Matys Z
Endokrinologie. 1976 Jul;67(3):373-6.
A case of a 26-year old woman suffering from an insulin resistant diabetes mellitus for 14 years is described. Acanthosis nigricans was diagnosed in the patient's second year and the syndrome of Stein-Leventhal at the age of 15. Diabetes could not be properly controlled either with the daily dosis of insulin as high as 1140 U or with peroral tolbutamide. Fasting serum IRI concentrations were elevated, the secretoric response to the stimulation by glucose or tolbutamide was substantial and protracted. The hypoglycemic response to the i.v. application of commercial insulin was insignificant. Serum growth hormone levels were normal. No presence of insulin antibodies in the serum was detected.
本文描述了一名26岁女性,患有胰岛素抵抗性糖尿病14年。患者在患病第二年被诊断出黑棘皮病,15岁时被诊断出斯坦因-莱文塔尔综合征。无论是每日高达1140单位的胰岛素剂量,还是口服甲苯磺丁脲,糖尿病都无法得到有效控制。空腹血清胰岛素放射免疫测定(IRI)浓度升高,对葡萄糖或甲苯磺丁脲刺激的分泌反应显著且持久。静脉注射商业胰岛素后的降糖反应不明显。血清生长激素水平正常。血清中未检测到胰岛素抗体。