Boon or Bane? Anti-Tumor Necrosis Factor Therapy Complicated by Listeria monocytogenes Meningitis Culminating in Colectomy for Ulcerative Colitis.

Ria Nagpal, Hemnaath Ulaganathan, Khushal Khan, Brian Egan
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Abstract

Anti-tumor necrosis factor (TNF) biologics have revolutionized the management of inflammatory bowel diseases (IBDs) by promoting mucosal healing and delaying surgical intervention in ulcerative colitis (UC). However, biologics can potentiate the risk of opportunistic infections alongside the use of other immunomodulators in IBD. As recommended by the European Crohn's and Colitis Organisation (ECCO), anti-TNF-α therapy should be suspended in the setting of a potentially life-threatening infection. The objective of this case report was to highlight how the practice of appropriately discontinuing immunosuppression can exacerbate underlying colitis. We need to maintain a high index of suspicion for complications of anti-TNF therapy, so that we can intervene early and prevent potential adverse sequelae. In this report, a 62-year-old female presented to the emergency department with non-specific symptoms including fever, diarrhea and confusion on a background of known UC. She had been commenced on infliximab (INFLECTRA®) 4 weeks earlier. Inflammatory markers were elevated, and Listeria monocytogenes was identified on both blood cultures and cerebrospinal fluid (CSF) polymerase chain reaction (PCR). The patient improved clinically and completed a 21-day course of amoxicillin advised by microbiology. After a multidisciplinary discussion, the team planned to switch her from infliximab to vedolizumab (ENTYVIO®). Unfortunately, the patient re-presented to hospital with acute severe UC. Left-sided colonoscopy demonstrated modified Mayo endoscopic score 3 colitis. She has had recurrent hospital admissions over the past 2 years for acute flares of UC, ultimately culminating in colectomy. To our knowledge, our case-based review is unique in unpacking the dilemma of holding immunosuppression at the risk of IBD worsening.

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恩还是贝恩?抗肿瘤坏死因子治疗合并单核细胞增生李斯特菌脑膜炎最终导致溃疡性结肠炎结肠切除术。
抗肿瘤坏死因子(TNF)生物制剂通过促进粘膜愈合和延迟溃疡性结肠炎(UC)的手术干预,彻底改变了炎症性肠病(IBDs)的治疗。然而,在IBD中,生物制剂与其他免疫调节剂一起使用可能会增加机会性感染的风险。根据欧洲克罗恩病和结肠炎组织(ECCO)的建议,在可能危及生命的感染情况下,抗tnf -α治疗应暂停。本病例报告的目的是强调适当停止免疫抑制的做法如何加剧潜在的结肠炎。我们需要对抗tnf治疗的并发症保持高度的怀疑指数,以便及早干预,预防潜在的不良后遗症。在本报告中,一名62岁女性以已知UC背景的非特异性症状,包括发烧、腹泻和精神错乱,来到急诊科。4周前开始使用英夫利昔单抗(INFLECTRA®)。炎症标志物升高,血培养和脑脊液(CSF)聚合酶链反应(PCR)均鉴定出单核细胞增生李斯特菌。患者临床好转,完成了微生物学建议的21天阿莫西林疗程。经过多学科讨论,该团队计划将她从英夫利昔单抗转为维多单抗(ENTYVIO®)。不幸的是,患者再次出现在医院急性严重UC。左侧结肠镜检查显示改良Mayo内镜评分为3分结肠炎。在过去的2年中,她因急性UC发作而反复住院,最终以结肠切除术告终。据我们所知,我们以病例为基础的回顾是独一无二的,它揭示了在IBD恶化风险下保持免疫抑制的困境。
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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