一名 2 岁儿童继发于胶原性结肠炎的蛋白丢失性肠病

JPGN reports Pub Date : 2024-02-06 DOI:10.1002/jpr3.12051
Hamza Hassan Khan, David N. Lewin, Carmine Suppa
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引用次数: 0

摘要

与胶原性结肠炎(CC)相关的蛋白丢失性肠病是一种罕见的疾病,但在成年人群中已有描述。然而,有关儿童患者的文献却很少。在此,我们描述了一名两岁女童的病例,她出现发热,伴有非血性水样腹泻,口服量减少。检查结果显示,她患有严重的低白蛋白血症(1.5 克/分升)、全血细胞减少以及粪便中α-1-抗胰蛋白酶升高(1.13 毫克/克)。内镜下胃肠道粘膜评估正常,但组织学检查结果与CC一致。她接受了为期 12 周的布地奈德治疗,症状和实验室值均有所缓解。目前,一年后她的病情没有复发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Protein‐losing enteropathy secondary to collagenous colitis in a 2‐year‐old
Protein‐losing enteropathy associated with collagenous colitis (CC) is a rare but described entity in the adult population. However, literature regarding this in the pediatric population is scarce. Here we describe a 2‐year‐old female who presented with fevers, accompanied by nonbloody, watery diarrhea, and decreased oral intake. Work‐up was significant for severe hypoalbuminemia at 1.5 grams per deciliter (g/dL), pancytopenia, and elevated fecal alpha‐1‐antitrypsin at 1.13 milligrams per grams (mg/g). Gastrointestinal mucosal evaluation was normal endoscopically; however, histology was consistent with CC. She responded to 12‐week treatment with budesonide with resolution of symptoms and laboratory values. At this point, she has not had a recurrence 1 year later.
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