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TNF-alpha antibody treatment in refractory collagenous sprue: report of a case and review of the literature.

机译:难治性胶原注射剂中的TNF-α抗体治疗:病例报告和文献复习。

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摘要

Collagenous sprue (CS) is a rare disease characterized by celiac type small bowel malabsorption that is resistant to gluten free diet (GFD) and is associated with a poor prognosis. Our aim was to assess the properties of the monoclonal TNF-alpha antibody infliximab in a patient with high-dose steroid refractory CS. A 27-year-old man developed watery diarrhea with weight loss and abdominal pain. Duodenal biopsies showed a subtotal villous atrophy with an extensive subepithelial layer of collagenous fibers. An apparent GFD did not reduce symptoms. High dose steroid treatment (75 mg prednisone) in combination with azathioprine (150 mg) reduced diarrhea but did not induce complete remission. Based on strongly elevated mucosal TNF-alpha transcript concentrations we introduced infliximab (5 mg/kg body weight) into therapy. After two applications the patient's symptoms quickly improved. During the following year no recurrence of diarrhea has been observed. This case suggests that infliximab is an effective treatment in complicated cases of collagenous sprue.
机译:胶原蛋白胶合剂(CS)是一种罕见疾病,其特征是腹腔型小肠吸收不良,对无麸质饮食(GFD)有抵抗力,并且预后不良。我们的目的是评估高剂量类固醇难治性CS患者的单克隆TNF-α抗体英夫利昔单抗的性质。一名27岁的男子出现水样腹泻,体重减轻和腹痛。十二指肠活检显示为小部分绒毛状萎缩,并具有广泛的上皮下胶原纤维层。明显的GFD并没有减轻症状。大剂量类固醇治疗(75毫克泼尼松)与硫唑嘌呤(150毫克)的组合可减少腹泻,但不能完全缓解。基于强烈升高的粘膜TNF-α转录物浓度,我们将英夫利昔单抗(5 mg / kg体重)引入治疗。两次应用后,患者的症状迅速改善。在接下来的一年中,没有观察到腹泻的复发。该病例表明英夫利昔单抗在复杂的胶原蛋白浇口病例中是一种有效的治疗方法。

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