Refractory Crohn's disease complicated with Guillain-Barré syndrome: A case report.

IF 1 4区 医学 Q3 MEDICINE, GENERAL & INTERNAL
A-Niu Liu, Jia-Yi Yang, Xing-Yu Chen, Shan-Shan Wu, Se-Niu Ji Zhi, Shu-Mei Zheng
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引用次数: 0

Abstract

Background: Inflammatory bowel disease (IBD) comprises a group of chronic inflammatory gastrointestinal disorders, including Crohn's disease (CD) and ulcerative colitis, with uncertain etiologies. The natural course of IBD can be accompanied by extraintestinal manifestations involving the skin, mucous membranes, musculoskeletal structures, eyes, cardiovascular system and nervous system. Guillain-Barré syndrome (GBS) is a type of peripheral neuropathy. However, the etiology and pathogenesis of IBD combined with GBS are unclear, and only a few clinical cases have been reported. Here, we report a case of refractory CD complicated by GBS and review the previous literature to improve the understanding of these diseases.

Case summary: A 34-year-old man had a 9-year history of refractory CD. He became unresponsive to multiple drugs and experienced recurrent intestinal fistulas. After several abdominal surgeries and treatment with ustekinumab, he achieved clinical remission. Unfortunately, he developed GBS during maintenance treatment with ustekinumab. According to previous reports, in some patients with IBD combined with GBS, GBS may be a comorbidity, an extraintestinal manifestation of IBD, or an adverse reaction to IBD therapeutic drugs. After a comprehensive evaluation, we suspected that GBS might have been a comorbidity in this patient. To avoid fatal disease relapse after medication discontinuation, we concluded that ustekinumab should not be withdrawn. On the basis of a joint decision between doctors and the patient, we decided to continue maintenance treatment with ustekinumab along with intravenous immunoglobulin, dexamethasone and traditional Chinese medicine acupuncture, which resulted in a steady improvement in his GBS symptoms and sustained remission of CD.

Conclusion: When IBD is complicated by a neurological disease, it is first necessary to analyze the patient's condition and then choose the corresponding treatment strategy. If the neurological disease is a specific comorbidity, treatment of both IBD and the comorbid disease should be considered. For IBD patients with extraintestinal manifestations involving the nervous system, neurological manifestations tend to resolve when the active IBD is controlled. When an adverse drug reaction is suspected, the medication should be discontinued, and symptomatic treatment should be administered.

难治性克罗恩病合并格林-巴罗综合征1例报告。
背景:炎症性肠病(IBD)包括一组慢性炎症性胃肠道疾病,包括克罗恩病(CD)和溃疡性结肠炎,病因不明。IBD的自然病程可伴有肠外表现,包括皮肤、粘膜、肌肉骨骼结构、眼睛、心血管系统和神经系统。格林-巴罗综合征(GBS)是一种周围神经病变。然而,IBD合并GBS的病因和发病机制尚不清楚,仅有少数临床病例报道。在此,我们报告一例难治性乳糜泻合并GBS,并回顾以往的文献,以提高对这些疾病的认识。病例总结:一名34岁男性,有9年难治性乳糜泻病史,对多种药物无反应,反复出现肠瘘。经过几次腹部手术和ustekinumab治疗,他达到了临床缓解。不幸的是,他在使用ustekinumab维持治疗期间患上了GBS。根据以往的报道,在一些IBD合并GBS的患者中,GBS可能是IBD的合并症,也可能是IBD的肠外表现,也可能是IBD治疗药物的不良反应。综合评估后,我们怀疑GBS可能是该患者的合并症。为了避免停药后致命性疾病复发,我们得出结论,ustekinumab不应停药。在医患共同决定的基础上,我们决定继续使用ustekinumab维持治疗,同时静脉注射免疫球蛋白、地塞米松和中医针灸,使他的GBS症状稳步改善,cd持续缓解。结论:当IBD合并神经系统疾病时,首先需要分析患者的病情,然后选择相应的治疗策略。如果神经系统疾病是一种特殊的合并症,则应考虑同时治疗IBD和合并症。对于肠外表现累及神经系统的IBD患者,当活动性IBD得到控制时,神经系统表现往往会消失。当怀疑发生药物不良反应时,应停药,并进行对症治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
World Journal of Clinical Cases
World Journal of Clinical Cases Medicine-General Medicine
自引率
0.00%
发文量
3384
期刊介绍: The World Journal of Clinical Cases (WJCC) is a high-quality, peer reviewed, open-access journal. The primary task of WJCC is to rapidly publish high-quality original articles, reviews, editorials, and case reports in the field of clinical cases. In order to promote productive academic communication, the peer review process for the WJCC is transparent; to this end, all published manuscripts are accompanied by the anonymized reviewers’ comments as well as the authors’ responses. The primary aims of the WJCC are to improve diagnostic, therapeutic and preventive modalities and the skills of clinicians and to guide clinical practice in clinical cases.
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