...
首页> 外文期刊>Case Reports in Pediatrics >Very Early-Onset Inflammatory Bowel Disease (VEO-IBD) Presenting with Recurrent Leukocytoclastic Vasculitis Preceded by Streptococcal Pharyngitis
【24h】

Very Early-Onset Inflammatory Bowel Disease (VEO-IBD) Presenting with Recurrent Leukocytoclastic Vasculitis Preceded by Streptococcal Pharyngitis

机译:非常早期的炎症性肠病(VEO-IBD)呈现出经复制的白细胞血管血管血管血管血管炎,其特点是链球菌咽炎

获取原文
           

摘要

Inflammatory bowel disease (IBD) that presents in children 6 years of age is known as very early-onset IBD (VEO-IBD). Extraintestinal manifestations in IBD, such as erythema nodosum (EN), pyoderma gangrenosum (PG), and, less likely, leukocytoclastic vasculitis (LV), are more commonly present in Crohn’s disease. Association between LV and ulcerative colitis (UC) is not commonly seen. We report a case of a 6-year-old female with a VEO-IBD UC phenotype presenting with multiple episodes of leukocytoclastic vasculitis, each preceded by streptococcal pharyngitis. Prior to the diagnosis of VEO-IBD, a skin biopsy was obtained and had shown leukocytoclastic vasculitis with a negative IgA stain. Initial laboratory results were remarkable for leukocytosis and increased anti-strep O and anti-DNase B titers. Gastrointestinal panel PCR demonstrated Clostridium difficile toxin A/B. Treatment for LV consisted of methylprednisolone IV 20?mg for four days with a weaning schedule of prednisolone for two weeks and naproxen 250?mg BID for three days. Clostridium difficile was treated with metronidazole 250?mg TID for ten days. She remained stable for three years until she presented with continuous bloody stools, newly onset chest pain, and shortness of breath. Computed tomography angiogram (CTA) was normal. Stool calprotectin was elevated at 658?mcg/gm. Abdominal magnetic resonance enterography (MRE), esophagogastroduodenoscopy, and colonoscopy confirmed a VEO-IBD ulcerative colitis phenotype. She was started on infliximab 10?mg/kg every four weeks after infliximab titers, and antibodies were obtained. Currently, the patient remains on clinical and biochemical remission, with no recent LV episodes or recurrence of streptococcal pharyngitis. Our patient is unique as no case report has been published with multiple episodes of leukocytoclastic vasculitis in association with a VEO-IBD UC phenotype.
机译:6岁被称为非常早发性IBD(VEO-IBD);在子&lt礼物炎症性肠病(IBD)。肠外表现在IBD,如结节性红斑(EN),坏疽性脓皮病(PG),和,不太可能,白细胞碎裂性血管炎(LV),更通常存在于克罗恩氏病。 LV和溃疡性结肠炎(UC)之间的关联并不常见。我们报道了6岁的女性有VEO-IBD UC表型白细胞碎裂性血管炎反复发作,每次由链球菌咽炎之前呈现的情况。之前VEO-IBD的诊断,获得皮肤活检,并示出为具有负的IgA染色白细胞碎裂血管炎。初步化验结果是显着的白细胞增多,增加抗链球菌O和抗DNA酶B滴度。胃肠面板PCR证实艰难梭菌毒素A / B。治疗LV包括甲泼尼龙IV 20的?毫克四天与泼尼松龙的两周断奶时间表和萘普生250?毫克BID三天。艰难梭菌用甲硝唑250?毫克TID十天治疗。她保持稳定了三年,直到她带有连续便血,新发病胸痛和呼吸急促。计算机断层扫描血管造影(CTA)是正常的。粪便钙网蛋白在658?微克/克升高。腹部磁共振小肠(MRE),食管胃,结肠镜检查证实VEO-IBD溃疡性结肠炎表型。她开始英夫利昔单抗10?毫克/公斤获得和抗体滴度英夫利昔单抗后,每四个星期。目前,患者仍对临床和生化缓解,近期没有LV发作或链球菌咽炎的复发。因为没有病例报告已经发表在了VEO-IBD UC表型协会白细胞碎裂性血管炎反复发作我们的病人是唯一的。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号