Department of Gastroenterology, Hampshire Hospitals NHS Foundation Trust, Winchester, United Kingdom.
J Crohns Colitis. 2013 Apr;7(3):e81-4. doi: 10.1016/j.crohns.2012.05.003. Epub 2012 May 29.
We present the case of a 16 year old girl who developed an aggressive colitis in the context of a prior biopsy proven autoimmune pancreatitis, which presented with obstructive jaundice at the age of 13 year. This history prompted prospective investigation and the discovery of compelling evidence to make a diagnosis of IgG4-related sclerosing disease with extra-pancreatic colonic involvement on the basis of raised serum IgG4 levels and a florid colonic IgG4 plasma cell infiltrate with over 20 IgG4 positive plasma cells/hpf. The colitis was resistant to conventional therapy but responded dramatically to treatment with the anti-TNFα monoclonal antibody, adalimumab. This is the first case to report both the effectiveness of adalimumab in treating IgG4 positive colitis in a patient with IgG4-related sclerosing disease, and to prospectively record resolution of an IgG4 positive colonic infiltrate with immunosuppression.
我们报告了一例 16 岁女孩的病例,该患者在先前经活检证实的自身免疫性胰腺炎的背景下发生侵袭性结肠炎,在 13 岁时表现为阻塞性黄疸。该病史促使我们进行了前瞻性研究,并发现了有力的证据,根据血清 IgG4 水平升高和结肠固有层 IgG4 浆细胞浸润(超过 20 个 IgG4 阳性浆细胞/高倍视野),做出了 IgG4 相关硬化性疾病伴胰腺外结肠受累的诊断。该结肠炎对常规治疗耐药,但对 TNF-α 单克隆抗体阿达木单抗治疗反应良好。这是首例报告 IgG4 相关硬化性疾病患者中,抗 TNF-α 单克隆抗体阿达木单抗治疗 IgG4 阳性结肠炎有效,以及前瞻性记录免疫抑制治疗后 IgG4 阳性结肠浸润消退的病例。