Suppr超能文献

一名黑色素瘤患者因接受低剂量干扰素-α治疗而引发1型糖尿病。

Type 1 diabetes mellitus caused by treatment with low-dose interferon-α in a melanoma patient.

作者信息

Sossau Daniel, Kofler Lukas, Eigentler Thomas

机构信息

Dermatology Department, University Hospital Tubingen, Tubingen, Germany.

出版信息

Melanoma Res. 2017 Oct;27(5):516-518. doi: 10.1097/CMR.0000000000000381.

Abstract

Interferon-α (INF-α) is used as an adjuvant treatment for high-risk cutaneous melanoma. It has a large variety of potentially severe and irreversible side effects and can contribute toward the development of autoimmune disease. We report a case of a 59-year-old woman who developed type 1 diabetes following the use of low-dose IFN-α for the adjuvant treatment of stage IIB melanoma. Fifteen months after initiating IFN-α, she presented with blood glucose of 1126 mg/dl, hyponatremia, and microalbuminuria. Antibodies to glutamic acid decarboxylase and islet antigen-2 were negative and C-peptide was markedly reduced. There was no personal or family history of any autoimmune conditions. Reinforced insulin treatment and volume substitution with saline and glucose as a counter-regulation was started. To the best of our knowledge, this is the first reported case of low-dose IFN-α-induced type 1 diabetes. Clinicians should closely evaluate the pros and cons of IFN-α treatment in an adjuvant setting and remain mindful of the possibility of drug-induced autoimmune disease.

摘要

干扰素-α(INF-α)被用作高危皮肤黑色素瘤的辅助治疗药物。它有多种潜在的严重且不可逆的副作用,并且可能促使自身免疫性疾病的发生。我们报告一例59岁女性病例,该患者在使用低剂量INF-α辅助治疗IIB期黑色素瘤后发生了1型糖尿病。开始使用INF-α 15个月后,她出现血糖1126mg/dl、低钠血症和微量白蛋白尿。谷氨酸脱羧酶抗体和胰岛抗原-2抗体均为阴性,C肽明显降低。患者无任何自身免疫性疾病的个人史或家族史。开始强化胰岛素治疗,并通过输注生理盐水和葡萄糖进行容量替代以进行对抗调节。据我们所知,这是首例关于低剂量INF-α诱发1型糖尿病的报道病例。临床医生在辅助治疗中应仔细评估INF-α治疗的利弊,并时刻留意药物诱发自身免疫性疾病的可能性。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验