Suppr超能文献

英夫利昔单抗治疗克罗恩病及随后发生的高安动脉炎

Treatment of Crohn's Disease With Infliximab and Subsequent Development of Takayasu's Arteritis.

作者信息

Nomura Kei, Shibuya Tomoyoshi, Furusho Momoko, Ishino Hirotaka, Orikasa Masayuki, Omori Masashi, Odakura Rina, Koma Masao, Ito Kentaro, Maruyama Takafumi, Ishikawa Dai, Hojo Mariko, Nagahara Akihito

机构信息

Department of Gastroenterology, Juntendo University School of Medicine, Bunkyo-ku, Tokyo 113-8421, Japan.

Department of Pathophysiological Research and Therapeutics for Gastrointestinal Disease, Juntendo University School of Medicine, Bunkyo-ku, Tokyo 113-8421, Japan.

出版信息

Gastroenterology Res. 2024 Dec;17(5-6):217-223. doi: 10.14740/gr1792. Epub 2024 Dec 28.

Abstract

A 23-year-old man was diagnosed with Crohn's disease (CD) of the large intestine after colonoscopy revealed longitudinal ulcers, and pathology revealed non-caseating epithelioid cell granulomas and anal fistulas. The CD relapsed, and therefore prednisolone (PSL) and infliximab (IFX) treatment was initiated. The PSL was gradually tapered. Steroid-free remission was maintained with IFX. The patient subsequently developed a high fever and headache, while CD-related symptoms did not worsen. Laboratory data showed white blood cells at 14,200/µL and C-reactive protein at 17.2 mg/dL. Contrast-enhanced computed tomography revealed thoracoabdominal aortitis, and the patient was consequently diagnosed with Takayasu's arteritis (TA). We therefore again initiated PSL treatment that immediately reduced the fever and headache. The PSL dose was again tapered and the administration of IFX was resumed to maintain CD remission. No further episodes of aortitis relapse were noted after restarting IFX, and the CD currently remains in remission. This is a rare case of TA onset during IFX treatment for CD, and, as such, contributes to the limited literature on such cases. More specifically, this case highlights that when patients with CD present with symptoms such as fever or headache, it is necessary to investigate the possibility of vasculitis.

摘要

一名23岁男性在结肠镜检查发现纵行溃疡且病理显示非干酪样上皮样细胞肉芽肿及肛瘘后,被诊断为大肠克罗恩病(CD)。CD复发,因此开始使用泼尼松龙(PSL)和英夫利昔单抗(IFX)治疗。PSL逐渐减量。IFX维持无类固醇缓解状态。该患者随后出现高热和头痛,而与CD相关的症状并未加重。实验室检查数据显示白细胞计数为14,200/µL,C反应蛋白为17.2 mg/dL。增强计算机断层扫描显示胸腹主动脉炎,该患者因此被诊断为高安动脉炎(TA)。于是我们再次开始使用PSL治疗,发热和头痛症状立即缓解。PSL剂量再次逐渐减量,并恢复使用IFX以维持CD缓解。重新使用IFX后未再出现主动脉炎复发情况,目前CD仍处于缓解状态。这是一例在IFX治疗CD期间发生TA的罕见病例,为此类病例的有限文献增添了内容。更具体地说,该病例强调,当CD患者出现发热或头痛等症状时,有必要调查血管炎的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d642/11711032/92093978ce80/gr-17-217-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