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首页> 外文期刊>Journal of pediatric gastroenterology and nutrition >Granulomatous Upper Gastrointestinal Inflammation in Pediatric Ulcerative Colitis
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Granulomatous Upper Gastrointestinal Inflammation in Pediatric Ulcerative Colitis

机译:小儿溃疡性结肠炎的粒状上胃肠炎症

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Objectives:Differentiating ulcerative colitis (UC) and Crohn disease (CD) can be clinically challenging, especially in children. Granulomatous inflammation has traditionally been attributed to CD. Crypt-associated giant cells and granulomas, however, have been observed in colonic biopsies of patients with UC. This phenomenon has not been described in the upper gastrointestinal (UGI) tract with UC.Methods:Seven pediatric patients with UC with granulomatous UGI (gUGI) lesions were identified. Diagnosis of UC was based on symptoms, clinical course, laboratory results, imaging, and endoscopy. We compared the gUGI patients to a large cohort of pediatric patients with UC (n=149).Results:All fully evaluated cases were associated with bloody diarrhea and moderate to severe pancolitis. Gastric and/or duodenal biopsies demonstrated giant cells or granulomas near gland destruction. Small bowel imaging did not reveal any involvement. The majority of cases responded to standard medical therapies, except for 2 patients (28.6%) who required total colectomy. Acute severe, refractory colitis (ie, colectomy within 1 month of presentation) was significantly more common in the gUGI group than the large pediatric UC group (28.6% vs 1.3%, Fisher exact P=0.01).Conclusions:This is the first report of pediatric UC-associated granulomatous inflammation in the UGI tract. We speculate that these lesions represent extracolonic manifestations of intense colonic disease. These atypical findings expand the diagnostic considerations that should be incorporated during the differentiation between UC and CD in the pediatric age group.
机译:目的:区分溃疡性结肠炎(UC)和CroHN病(CD)可以临床挑战,特别是在儿童中。传统上肉芽肿炎症归因于CD。然而,已经在UC患者的结肠活组织检查中观察到隐窝相关的巨细胞和肉芽肿。尚未在UC中的上胃肠道(UGI)道中描述这种现象UC的诊断基于症状,临床过程,实验室结果,成像和内窥镜检查。我们将Gugi患者与UC(n = 149)的大量儿科患者进行比较胃和/或十二指肠活组织检查显示巨型细胞或肉芽肿附近的腺体破坏。小肠成像没有透露任何参与。大多数案件应对标准的医疗疗法作出反应,除2名患者(28.6%)外,均需要完全联络。急性严重,难治性结肠炎(即1个月内的联合肌瘤)在Gugi组中比大型儿科UC组显着更常见(28.6%vs 1.3%,Fisher精确P = 0.01).Conclusions:这是第一个报告ugi道中儿科UC相关肉芽肿炎症。我们推测,这些病变代表了强烈结肠疾病的胚性表现。这些非典型调查结果扩展了在儿科年龄组中的UC和CD之间的差异期间应掺入的诊断考虑。

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