Queliza Karen, Ihekweazu Faith D, Schady Deborah, Jensen Craig, Kellermayer Richard
Department of Pediatric Gastroenterology, Hepatology and Nutrition.
Department of Pediatric Pathology, Baylor College of Medicine-Texas Children's Hospital.
J Pediatr Gastroenterol Nutr. 2018 Apr;66(4):620-623. doi: 10.1097/MPG.0000000000001771.
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.
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).
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).
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.
鉴别溃疡性结肠炎(UC)和克罗恩病(CD)在临床上具有挑战性,尤其是在儿童患者中。传统上,肉芽肿性炎症被认为是CD的特征。然而,在UC患者的结肠活检中也观察到了隐窝相关巨细胞和肉芽肿。UC在上消化道(UGI)中的这种现象尚未见报道。
确定了7例患有上消化道肉芽肿性病变(gUGI)的儿童UC患者。UC的诊断基于症状、临床病程、实验室检查结果、影像学检查和内镜检查。我们将gUGI患者与一大群儿童UC患者(n = 149)进行了比较。
所有经过全面评估的病例均伴有血性腹泻和中度至重度全结肠炎。胃和/或十二指肠活检显示在腺体破坏附近有巨细胞或肉芽肿。小肠影像学检查未发现任何受累情况。除2例(28.6%)需要行全结肠切除术的患者外,大多数病例对标准药物治疗有反应。gUGI组急性重症难治性结肠炎(即就诊后1个月内行结肠切除术)的发生率显著高于大型儿童UC组(28.6%对1.3%,Fisher确切概率法P = 0.01)。
这是关于儿童UC相关上消化道肉芽肿性炎症的首次报道。我们推测这些病变代表了严重结肠疾病的结肠外表现。这些非典型发现扩展了在儿童年龄组中UC和CD鉴别诊断时应考虑的诊断因素。