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IgG4-negative autoimmune pancreatitis with sclerosing cholangitis and colitis: possible association with primary sclerosing cholangitis?

机译:IgG4阴性的自身免疫性胰腺炎合并硬化性胆管炎和结肠炎:可能与原发性硬化性胆管炎有关吗?

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摘要

We report a case of autoimmune pancreatitis (AIP) with cholangiography and histopathology showing features characteristic of primary sclerosing cholangitis (PSC) and colitis. A 55-year-old previously-healthy man was diagnosed with anti-nuclear antibody (ANA)-positive AIP according to the finding of serum biochemistry, abdominal US (ultrasonography), CT (computed tomography) and ERCP (endoscopic retrograde cholangiopancreatography). However, bead-like strictures of intrahepatic bile ducts were also found and liver tissue showed onion skin-like periductal fibrosis but no anti-IgG4-positive cells. In addition, colon fiberscopy showed a pancolitis similar to ulcerative colitis indicating that, in this case, there may be an association with PSC. Here, we report a rare case of IgG4-negative AIP with sclerosing cholangitis and colitis with many clinical features that support an association with PSC.
机译:我们报告一例自身免疫性胰腺炎(AIP)的胆管造影和组织病理学表现为原发性硬化性胆管炎(PSC)和结肠炎的特征。根据血清生物化学,腹部US(超声),CT(计算机断层扫描)和ERCP(内镜逆行胰胆管造影)的发现,一名55岁以前健康的人被诊断出抗核抗体(ANA)阳性。但是,还发现了肝内胆管的珠状狭窄,并且肝组织显示出洋葱皮样导管周围纤维化,但没有抗IgG4阳性细胞。此外,结肠纤维镜检查显示出类似于溃疡性结肠炎的全结肠炎,表明在这种情况下,可能与PSC有关。在这里,我们报道了一种罕见的IgG4阴性AIP合并硬化性胆管炎和结肠炎的临床特征,这些特征支持与PSC的关联。

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