Norris Logan, Giroux Parker, Jester Traci, Galloway David P, Maclin Jeanine, Saaybi Stephanie, Hill Benjamin, Medina Perez Mariangeles, Dike Chinenye R
Heersink School of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA.
Department of Pediatrics, Division of Pediatric Gastroenterology, Hepatology and Nutrition, University of Alabama at Birmingham, Birmingham, AL, USA.
Am J Case Rep. 2025 Feb 28;26:e946099. doi: 10.12659/AJCR.946099.
BACKGROUND The incidence of Crohn's disease (CD) has increased worldwide. Although common presenting symptoms of CD in children include abdominal pain, diarrhea, and rectal bleeding, it can also present atypically and can have extraintestinal manifestations. Isolated upper-gastrointestinal bleed as the only manifestation of CD with ileocolonic involvement is rare. CASE REPORT We describe the case of a previously healthy, 9-year-old boy who presented to the emergency department (ED) with isolated, acute-onset hematemesis. He was evaluated in the ED, and found to be hemodynamically stable, and hematemesis had resolved upon arrival to the ED. Therefore, he was placed on a proton pump inhibitor (PPI), and discharged with a close gastrointestinal clinic follow-up, which he missed. He returned to the ED 3 weeks later with another episode of hematemesis with hemodynamic instability requiring resuscitation and intensive care unit stay. He underwent an emergency esophagogastroduodenoscopy (EGD), which revealed a bleeding gastric ulcer in the fundus. Bleeding was controlled with epinephrine injection and application of hemostatic clips. Gastric biopsies revealed granulomas. Therefore, during his hospitalization, ileocolonoscopy was completed to rule out CD. Ileocolonoscopy showed left colonic edema with ulcers and terminal ileal ulcers with exudates. Histopathology revealed granulomas in these areas. Infliximab infusions were started during the hospitalization. He is currently receiving 10 mg/kg of infliximab every 4 weeks. CONCLUSIONS This case highlights the need for increased clinician awareness of atypical presentations of inflammatory bowel disease (IBD) and maintenance of a high index of suspicion when treating children and adolescents with acute GI bleed.
背景 克罗恩病(CD)的发病率在全球范围内呈上升趋势。尽管儿童CD的常见症状包括腹痛、腹泻和直肠出血,但也可能表现不典型且出现肠外表现。孤立性上消化道出血作为累及回结肠的CD的唯一表现较为罕见。病例报告 我们描述了一名既往健康的9岁男孩的病例,他因孤立性急性呕血就诊于急诊科(ED)。他在ED接受了评估,发现血流动力学稳定,到达ED时呕血已缓解。因此,给他使用了质子泵抑制剂(PPI),并安排密切的胃肠病门诊随访,但他失访了。3周后他因再次呕血且伴有血流动力学不稳定返回ED,需要进行复苏并入住重症监护病房。他接受了急诊食管胃十二指肠镜检查(EGD),结果显示胃底有一处出血性溃疡。通过肾上腺素注射和应用止血夹控制了出血。胃活检显示有肉芽肿。因此,在他住院期间,完成了回结肠镜检查以排除CD。回结肠镜检查显示左结肠水肿伴溃疡,末端回肠溃疡伴渗出物。组织病理学显示这些部位有肉芽肿。住院期间开始使用英夫利昔单抗输注。他目前每4周接受10 mg/kg的英夫利昔单抗治疗。结论 本病例强调临床医生需要提高对炎症性肠病(IBD)非典型表现的认识,并在治疗急性胃肠道出血的儿童和青少年时保持高度的怀疑指数。