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英夫利昔单抗治疗小儿难治性克罗恩病:一例报告

Infliximab treatment of pediatric refractory Crohn's disease: a case report.

作者信息

Akman Sezin Aşik, Arikan Ciğdem, Sözen Gülben, Oztürk Can, Yağci Raflit Vural

机构信息

Department of Pediatric Gastroenterology, Hepatology and Nutrition Unit, Tepecik Teaching Hospital, Izmir, Turkey.

出版信息

Turk J Gastroenterol. 2006 Jun;17(2):133-6.

Abstract

Infliximab is a monoclonal antibody that targets TNF-alpha and has been shown to be effective for the management of steroid-dependent or refractory Crohn's disease. It is an effective therapy in adult patients, but experience in children is limited. We report a case of Crohn's disease which was refractory to the conventional treatment. A 14-year-old boy was admitted to the hospital with arthralgia and oral and perianal lesions. On physical examination his body weight was below the 3rd percentile, and height was between the 3rd-10th percentiles. He had elevated erythrocyte sedimentation rate and C-reactive protein and decreased hemoglobin, hematocrit and albumin levels. Barium enema and computerized abdominal tomography revealed a markedly distended small bowel with a narrowed area just above the ileocecal valve and terminal ileum. There was no mucosal pathology in his colonoscopic study. A regimen of prednisolone was begun with a diagnosis of Crohn's disease. In the first month of therapy the patient experienced progressive worsening of his symptoms, and azathioprine was added to the treatment in the second month. As he had exacerbation of his symptoms and worsening laboratory tests, infliximab infusions (5 mg/kg/d) were administered intravenously (at 0, 2 and 6 weeks) at the end of the 8th week. At the 6th week of treatment including two infusions of infliximab at 0 and 2 weeks, clinical and laboratory response occurred. The only side effect of the treatment was pneumonia, which was seen after the 6th week of the therapy. In conclusion, infliximab appears to be an effective and safe therapy for childhood refractory Crohn's disease.

摘要

英夫利昔单抗是一种靶向肿瘤坏死因子-α的单克隆抗体,已被证明对激素依赖型或难治性克罗恩病的治疗有效。它在成年患者中是一种有效的治疗方法,但在儿童中的经验有限。我们报告一例对传统治疗无效的克罗恩病病例。一名14岁男孩因关节痛、口腔及肛周病变入院。体格检查发现其体重低于第3百分位,身高在第3至第10百分位之间。他的红细胞沉降率和C反应蛋白升高,血红蛋白、血细胞比容和白蛋白水平降低。钡剂灌肠和腹部计算机断层扫描显示小肠明显扩张,回盲瓣上方和回肠末端有狭窄区域。结肠镜检查未发现结肠黏膜病变。诊断为克罗恩病后开始使用泼尼松龙治疗方案。在治疗的第一个月,患者症状逐渐加重,第二个月加用硫唑嘌呤治疗。由于他的症状加重且实验室检查结果恶化,在第8周结束时静脉输注英夫利昔单抗(5mg/kg/d)(分别在第0、2和6周)。在包括第0周和第2周两次输注英夫利昔单抗的治疗第6周时,出现了临床和实验室反应。治疗的唯一副作用是在治疗第6周后出现的肺炎。总之,英夫利昔单抗似乎是治疗儿童难治性克罗恩病的一种有效且安全的疗法。

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