Suppr超能文献

家族性2型糖尿病合并甲状腺功能减退及多种自身免疫性疾病1例报告

A case report of familial type 2 diabetes mellitus combined with hypothyroidism and multiple autoimmune diseases.

作者信息

Su Xuan, Yang Yang, Jiang Haotian, Lai Xiuchang, Qu Yujia

机构信息

The First Clinical College, Wuhan University of Science and Technology, Wuhan, China.

Department of Endocrinology, Tianyou Hospital Affiliated to Wuhan University of Science and Technology, Wuhan, China.

出版信息

Front Endocrinol (Lausanne). 2025 Aug 4;16:1599546. doi: 10.3389/fendo.2025.1599546. eCollection 2025.

Abstract

Gene mutations in the Janus kinase/signal transducer and activator of transcription signaling (JAK/STAT) pathway can promote the occurrence of type 2 diabetes mellitus (T2DM) and autoimmune diseases. We report on two patients with T2DM (a mother and her adult son) with concomitant Hashimoto's thyroiditis and autoimmune diseases. The son was diagnosed with systemic sclerosis and antiphospholipid syndrome, while the mother was diagnosed with primary biliary cholangitis. Both diagnoses occurred simultaneously. These cases highlight that, in clinical practice, careful symptom assessment, thorough history-taking, standardized physical examination, and obtaining a detailed family history are important. This reduces the misdiagnosis and missed diagnosis rates, enabling early diagnosis and treatment, thereby improving patient outcomes. While genetic testing was not performed in these two patients, this represents a potential direction for future research.

摘要

Janus激酶/信号转导子和转录激活子信号通路(JAK/STAT)中的基因突变可促进2型糖尿病(T2DM)和自身免疫性疾病的发生。我们报告了两名患有T2DM的患者(一位母亲和她成年的儿子),他们同时患有桥本甲状腺炎和自身免疫性疾病。儿子被诊断为系统性硬化症和抗磷脂综合征,而母亲被诊断为原发性胆汁性胆管炎。这两种诊断同时出现。这些病例表明,在临床实践中,仔细的症状评估、全面的病史采集、规范的体格检查以及获取详细的家族史很重要。这可降低误诊和漏诊率,实现早期诊断和治疗,从而改善患者的预后。虽然这两名患者未进行基因检测,但这代表了未来研究的一个潜在方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ce6/12358270/372807f5f9c7/fendo-16-1599546-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验