Infliximab monotherapy for ulcerative colitis-related severe enteritis following colectomy in a paediatric patient.

IF 0.6 Q3 MEDICINE, GENERAL & INTERNAL
Mohana Sathiaseelan, Kei Yu Chiu, Alicia Lim, Madhur Ravikumara
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引用次数: 0

Abstract

We report the rare entity of ulcerative colitis-related severe enteritis (UCRSE) following colectomy in a child. This entity has been described primarily in adults and is characterised by diffuse enteritis with histology identical to ulcerative colitis (UC). The mainstay treatment is steroids and in recent years anti-tumour necrosis factor agents.A boy in early adolescence required urgent colectomy for medically refractory severe acute colitis. Colectomy specimen histology confirmed UC. Postoperatively, he developed fevers, severe abdominal pain and excessive stoma output (5 L/day). Endoscopy revealed severe extensive enteritis, histologically resembling UC. Infliximab (IFX) was commenced with significant improvement. He remains asymptomatic 28 months post-colectomy on maintenance IFX monotherapy. To our knowledge, this is the youngest patient with this complication.This case illustrates the need to consider UCRSE in a child with otherwise unexplained fever, severe abdominal pain and high stoma output post colectomy. IFX monotherapy is a successful treatment option.

英夫利西单抗治疗一名儿童结肠切除术后溃疡性结肠炎相关重症肠炎。
我们报告了儿童结肠切除术后发生溃疡性结肠炎相关重症肠炎 (UCRSE) 的罕见病例。这种病症主要发生在成年人身上,其特点是弥漫性肠炎,组织学与溃疡性结肠炎(UC)相同。该病的主要治疗方法是类固醇,近年来还使用抗肿瘤坏死因子药物。一名青春期早期的男孩因药物难治性严重急性结肠炎而需要紧急进行结肠切除术。结肠切除术标本组织学证实为 UC。术后,他出现发烧、剧烈腹痛和造口排出量过大(每天 5 升)。内镜检查发现他患有严重的广泛性肠炎,组织学上类似于 UC。开始使用英夫利西单抗(IFX)后,病情明显好转。结肠切除术后 28 个月,他仍无症状,一直接受 IFX 单药治疗。据我们所知,这是年龄最小的并发症患者。该病例说明,对于结肠切除术后不明原因发热、剧烈腹痛和造口排出量高的患儿,有必要考虑 UCRSE。IFX 单一疗法是一种成功的治疗方案。
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
BMJ Case Reports
BMJ Case Reports Medicine-Medicine (all)
CiteScore
1.40
自引率
0.00%
发文量
1588
期刊介绍: BMJ Case Reports is an important educational resource offering a high volume of cases in all disciplines so that healthcare professionals, researchers and others can easily find clinically important information on common and rare conditions. All articles are peer reviewed and copy edited before publication. BMJ Case Reports is not an edition or supplement of the BMJ.
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