儿童非食道嗜酸性粒细胞性胃肠道疾病和慢性腹痛:一项多中心研究

Bhaswati C Acharyya, Meghdeep Mukhopadhyay, Hema Chakrabarty
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引用次数: 0

摘要

背景:在发展中国家,嗜酸性粒细胞性食管炎之外的嗜酸性粒细胞性胃肠道疾病(EGID)并不常见。目的:估计在一组患有非功能性慢性腹痛(CAP)的儿童患者中EGID的患病率。方法:回顾性分析小儿CAP的病例记录,对表现出临床或实验室警示特征的患儿进行内镜评估。上消化道内窥镜和回肠结肠镜的组织病理学报告确定了EGID的诊断。随后的分析包括临床表现、儿童或家庭中特应性的存在、血红蛋白、白蛋白、血清免疫球蛋白E (IgE)、粪便钙保护蛋白水平、内窥镜表现、治疗方法和结果。结果:对368例有机CAP患儿进行了内镜检查。其中19例(5.2%)CAP患者被诊断为EGID。儿童的中位年龄为11.1岁(四分位数间距= 8.4-14.4)。5岁以上有机CAP儿童中EGID的估计患病率为520/10000。脐周疼痛是最常见的部位(63%)。特应性家族史、外周血嗜酸性粒细胞增多和血清IgE升高是与EGID显著相关的三个参数。所有患儿在6个月时均获得临床缓解。47%的患者有微小的缓解,并且持续到1年的随访。6个月后,53%的患者出现了波动的临床病程。结论:食管外的EGID在印度儿童中并不少见。对小儿CAP的病因有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Non-esophageal eosinophilic gastrointestinal disease and chronic abdominal pain in children: A multicenter experience.

Background: Eosinophilic gastrointestinal (GI) disease (EGID) beyond eosinophilic esophagitis is not commonly reported in the developing world.

Aim: To estimate the prevalence of EGID in a selected group of pediatric patients suffering from non-functional chronic abdominal pain (CAP).

Methods: A retrospective analysis was conducted on case records of children with CAP. Those exhibiting clinical or laboratory alarming features underwent endoscopic evaluation. Histopathology reports from upper GI endoscopy and ileo-colonoscopy determined the diagnosis of EGID. Subsequent analyses included clinical presentations, presence of atopy in the children or family, hemoglobin, albumin, serum immunoglobulin E (IgE), fecal calprotectin levels, endoscopic appearances, treatment methods, and outcomes.

Results: A total of 368 children with organic CAP were subjected to endoscopic evaluation. Among them, 19 (5.2%) patients with CAP were diagnosed with EGID. The median age of the children was 11.1 years (interquartile range = 8.4-14.4). The estimated prevalence of EGID in children with organic CAP was 520/10000 children over 5 years. Periumbilical pain was the most common site (63%). Family history of atopy, peripheral blood eosinophilia, and elevated serum IgE were the three parameters significantly associated with EGID. Clinical remission was obtained in all children at 6 months. The 47% had microscopic remission and maintained remission until a 1-year follow-up. The 53% had a fluctuating clinical course after 6 months.

Conclusion: EGID beyond the esophagus is not an uncommon entity among the children of India. It can contribute significantly to the etiology of pediatric CAP.

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