口腔溃疡和胃肠道出血的挑战性病例:克罗恩病或贝氏病。

IF 0.7 Q4 PEDIATRICS Case Reports in Pediatrics Pub Date : 2023-10-04 eCollection Date: 2023-01-01 DOI:10.1155/2023/4705638
Marina A S Dantas, Ana Luiza Graneiro, Rodrigo Cavalcante, Lina Maria Felipez
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摘要

介绍将克罗恩病(CD)和贝氏病(BD)与胃肠道(GI)表现区分开来在临床上可能具有挑战性,因为目前两种情况的诊断标准尚不清楚,多种症状可能重叠。案例介绍。患者是一名8岁的巴西裔男孩,最初有1年的口腔溃疡疼痛史。在入院之前,他曾接受过周期性发烧、口口炎、咽炎和腺炎的治疗,并服用了类固醇,在尝试戒药时出现复发症状。最初的检查基本上不起眼。口腔活检显示没有肉芽肿,眼科检查正常。传染病和风湿病测试均为阴性。普罗米修斯IBD sgi测试显示出与CD一致的模式;然而,患者有多次阴性内镜检查、结肠镜检查和胶囊内镜检查。他出现间歇性便血和严重营养不良,对英夫利昔单抗、秋水仙碱或甲氨蝶呤没有反应。在大的胃肠道出血后,进行了第四次结肠镜检查,结果显示回肠末端有大的圆形溃疡,没有肉芽肿。他开始服用ustekinumab,临床症状有所改善。一个月后,他出现双侧髋关节积液和脑膜炎,被诊断为新冠肺炎继发无菌性脑膜炎。他的病情有所好转,但一个月后症状恶化,MRV显示广泛的静脉窦血栓形成。患者开始服用依诺肝素、甲基强的松龙和秋水仙碱,在3个月的随访中血栓消退。患者的总体症状得到控制,每月使用ustekinumab后临床和生化症状得到缓解。讨论和结论。我们的患者经历了一个具有挑战性的临床过程,有非特异性的全身和肠道表现,很难区分BD和CD。考虑到新冠肺炎后内窥镜检查结果和胃肠道症状控制的患者中枢神经系统自炎反应的恶化,最有可能的诊断是BD。
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A Challenging Case of Oral Ulcers and Gastrointestinal Bleeding: Crohn's or Behçet's Disease.

Introduction. Differentiating Crohn's disease (CD) and Behçet's disease (BD) with gastrointestinal (GI) manifestations can be clinically challenging, as current diagnostic criteria are not clear between both conditions and multiple symptoms could overlap. Case Presentation. The patient is an 8-year-old boy of Brazilian descent, who initially presented with a 1-year history of painful oral ulcers. Before presenting to the hospital, he had been treated for periodic fever, aphthous stomatitis, pharyngitis, and adenitis and placed on steroids, with relapsing symptoms on attempts to wean the doses. The initial workup was largely unremarkable. Buccal biopsies showed no granulomas, and the ophthalmologic exam was normal. Infectious and rheumatological tests were negative. Prometheus IBD sgi testing showed a pattern consistent with CD; however, the patient had multiple negative endoscopies, colonoscopies, and capsule endoscopies. He developed intermittent bloody stools and severe malnutrition and did not respond to infliximab, colchicine, or methotrexate. After a large GI bleed, a 4th colonoscopy was performed, which showed large round ulcers in the terminal ileum, and no granulomas. He was started on ustekinumab with clinical improvement. One month later, he developed bilateral hip effusion and meningismus, being diagnosed with aseptic meningitis secondary to COVID-19. He improved, but in one month developed worsening symptoms, and MRV showed extensive venous sinus thrombosis. The patient was started on enoxaparin, methylprednisolone, and colchicine, with resolution of the thrombus on a 3-month follow-up. The patient's overall symptoms remained controlled with clinical and biochemical remission on monthly ustekinumab. Discussion and Conclusion. Our patient had a challenging clinical course, with nonspecific systemic and intestinal manifestations which proved difficult to differentiate between BD and CD. Given endoscopic findings and the worsening of an auto-inflammatory reaction in the central nervous system after COVID-19 in a patient with controlled GI symptoms, the most likely diagnosis is BD.

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审稿时长
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