首页> 美国卫生研究院文献>Case Reports in Gastroenterology >Sarcoidosis of the Intra- and Extrahepatic Bile Ducts with Concomitant Cholangitis in a Patient with Ulcerative Colitis
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Sarcoidosis of the Intra- and Extrahepatic Bile Ducts with Concomitant Cholangitis in a Patient with Ulcerative Colitis

机译:溃疡性结肠炎患者伴有胆管炎的肝内和肝外胆管结节病

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摘要

Cholangitis in patients with ulcerative colitis (UC) can lead to misdiagnosis of primary sclerosing cholangitis (PSC). Furthermore, it can mimic cholangiocellular carcinoma, which also can lead to inappropriate and potentially harmful treatment of the patient. An 18-year-old male patient with known UC presented with pain in his right upper abdomen and elevation of the cholestatic liver enzymes (alkaline phosphatase: 197 U/L, γ-glutamyltransferase: 229 U/L) and increased inflammatory parameters (leukocytosis and CrP of 13.6 mg/L). Magnetic resonance cholangiopancreatography revealed unclear stenosis in the bifurcation of the main hepatic bile duct as well as in the prepapillary bile duct. Ultrasound (US) examination and endoscopic retrograde cholangiopancreatography showed dilatation of the intra -and extrahepatic bile ducts, which raised the suspicion of PSC. US image with dilated intra- and extrahepatic dilatation of the bile duct was also suggestive for autoimmune cholangitis. However, serum analysis revealed an elevated soluble interleukin-II receptor (1,305 U/mL), while immunoglobulin G4 was within normal ranges. Liver biopsy demonstrated hepatic inflammation and presence of granulomatous cells within the portal fields – convenient to sarcoidosis. After starting treatment with steroids, we observed a rapid clinical response with improvement of the dilated bile ducts and decrease of the initially elevated cholestatic liver enzymes. Sarcoidosis within the bile duct is a rare condition. Steroids are the treatment of choice and – along with the histology – are furthermore helpful to differentiate between several potential differential diagnoses like IgG4 cholangitis, primary biliary cholangitis, or PSC.
机译:溃疡性结肠炎(UC)患者的胆管炎可导致对原发性硬化性胆管炎(PSC)的误诊。此外,它可以模仿胆管细胞癌,这也可能导致对患者的不适当的治疗以及可能有害的治疗。一名已知UC的18岁男性患者,其右上腹疼痛且胆汁淤积性肝酶(碱性磷酸酶:197 U / L,γ-谷氨酰转移酶:229 U / L)升高,并且炎症参数增加(白细胞增多) CrP为13.6 mg / L)。磁共振胰胆管造影显示主肝胆管分叉以及乳头前胆管的狭窄狭窄。超声(US)检查和内镜逆行胰胆管造影显示肝内和肝外胆管扩张,这引起了对PSC的怀疑。胆管内和肝外扩张的超声图像也提示自身免疫性胆管炎。但是,血清分析显示可溶性白介素II受体升高(1305 U / mL),而免疫球蛋白G4在正常范围内。肝活检显示肝炎和门脉区域内肉芽肿细胞的存在–便于结节病。在开始使用类固醇治疗后,我们观察到了快速的临床反应,其中胆管扩张的情况有所改善,而最初胆汁淤积性肝酶升高的情况有所减少。胆管内结节病是一种罕见病。类固醇是一种选择的治疗方法,并且与组织学一起有助于进一步区分几种潜在的鉴别诊断,例如IgG4胆管炎,原发性胆管性胆管炎或PSC。

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