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甲巯咪唑和卡比马唑治疗的格雷夫斯病患者中的胰岛素自身免疫综合征:一例报告

Insulin autoimmune syndrome in a patient with methimazole and carbimazole-treated Graves' disease: a case report.

作者信息

Lu C C, Lee J K, Lam H C, Yang C Y, Han T M

机构信息

Department of Medicine, National Yang-Ming University, Taipei, Taiwan, R.O.C.

出版信息

Zhonghua Yi Xue Za Zhi (Taipei). 1994 Nov;54(5):353-8.

PMID:7834559
Abstract

Insulin autoimmune syndrome (IAS) includes fasting or reactive hypoglycemia, hyperinsulinemia and the presence of insulin-binding antibodies in patients who have never been exposed to exogenous insulin. The report concerns a 34-year-old male patient with Graves' disease who had history of having taken methimazole for two months, without any consequence, 4 years previously. However, when methimazole was again administered for three weeks followed by a week of carbimazole, the patient suffered hypoglycemia 4 times during the next 4 weeks. He denied history of diabetes mellitus (DM), of taking any oral hypoglycemic agent or of having received insulin injection. Laboratory data showed total serum insulin level > 320 microU/mL, free insulin 55 microU/mL and insulin antibody 88.3%. Oral glucose tolerance test (OGTT) revealed DM pattern. Since the patient had history of allergy to anti-thyroid drugs before this event, so he was treated with radioiodine (131I). There was no episode of hypoglycemic attack during 15 months of follow-up.

摘要

胰岛素自身免疫综合征(IAS)包括空腹或反应性低血糖、高胰岛素血症,以及从未接触过外源性胰岛素的患者体内存在胰岛素结合抗体。本文报告了一名34岁患有格雷夫斯病的男性患者,该患者4年前曾服用甲巯咪唑两个月,未出现任何不良反应。然而,当再次服用甲巯咪唑三周,随后服用卡比马唑一周后,患者在接下来的4周内出现了4次低血糖。他否认有糖尿病(DM)病史、服用过任何口服降糖药或接受过胰岛素注射。实验室数据显示血清总胰岛素水平>320微单位/毫升,游离胰岛素55微单位/毫升,胰岛素抗体88.3%。口服葡萄糖耐量试验(OGTT)显示为糖尿病模式。由于该患者在此事件发生前有抗甲状腺药物过敏史,因此接受了放射性碘(131I)治疗。在15个月的随访期间未发生低血糖发作。

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