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首页> 外文期刊>AJR: American Journal of Roentgenology : Including Diagnostic Radiology, Radiation Oncology, Nuclear Medicine, Ultrasonography and Related Basic Sciences >Comparative MRI analysis of morphologic patterns of bile duct disease in IgG4-related systemic disease versus primary sclerosing cholangitis
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Comparative MRI analysis of morphologic patterns of bile duct disease in IgG4-related systemic disease versus primary sclerosing cholangitis

机译:IgG4相关系统性疾病与原发性硬化性胆管炎的胆管疾病形态学模式的MRI比较分析

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OBJECTIVE. The purpose of this study was to perform a retrospective MRI-based comparative analysis of the morphologic patterns of bile duct disease in IgG4-related systemic disease (ISD, also called autoimmune pancreatitis) compared with primary sclerosing cholangitis (PSC) and the autoimmune liver diseases autoimmune hepatitis and primary biliary cirrhosis. MATERIALS AND METHODS. This study included 162 consecutively registered patients (47 with ISD, 73 with PSC, and 42 with autoimmune liver diseases). Two abdominal radiologists retrospectively reviewed MR images in consensus. Imaging findings on the bile ducts, liver, pancreas, and other organs were analyzed to establish disease patterns. RESULTS. ISD was associated with contiguous thickening of intrahepatic and extrahepatic bile ducts (p < 0.001), pancreatic parenchymal abnormalities (p < 0.001), renal abnormalities (p < 0.001), and gallbladder wall thickening (p < 0.03). The severity of common bile duct wall thickness was significantly different in ISD (p < 0.001). The mean single wall thickness in the ISD group was 3.00 (SD, 1.47) mm, in the PSC group was 1.89 (SD, 0.73) mm, and in the autoimmune liver disease group was 1.80 (SD, 0.67) mm. PSC was associated with liver parenchymal abnormalities (p < 0.001). We did not find statistical significance between the three groups in location (p = 0.220) or length (p = 0.703) of extrahepatic bile duct strictures, enhancement of bile duct stricture (p = 0.033), upper abdominal lymphadenopathy, or retroperitoneal fibrosis. Although presence of intrahepatic bile duct stricture was statistically significant when all three groups were compared, it was not useful for differentiating ISD from PSC. CONCLUSION. The presence of continuous as opposed to skip disease in the bile ducts, gallbladder involvement, and single-wall common bile duct thickness greater than 2.5 mm supports a diagnosis of ISD over PSC. ISD and PSC could not be differentiated on the basis of location and length of common bile duct stricture.
机译:目的。这项研究的目的是对与原发性硬化性胆管炎(PSC)和自身免疫性肝病相比的IgG4相关系统疾病(ISD,也称为自身免疫性胰腺炎)胆管疾病的形态学模式进行基于MRI的回顾性比较分析。自身免疫性肝炎和原发性胆汁性肝硬化。材料和方法。这项研究包括162位连续登记的患者(47位ISD,73位PSC和42位自身免疫性肝病患者)。两位腹部放射科医生一致地回顾了MR图像。分析胆管,肝脏,胰腺和其他器官的影像学发现以建立疾病模式。结果。 ISD与肝内和肝外胆管连续增厚(p <0.001),胰腺实质异常(p <0.001),肾脏异常(p <0.001)和胆囊壁增厚(p <0.03)有关。在ISD中,胆总管壁厚的严重程度显着不同(p <0.001)。 ISD组的平均单壁厚度为3.00(SD,1.47)mm,PSC组为1.89(SD,0.73)mm,自身免疫性肝病组为1.80(SD,0.67)mm。 PSC与肝实质异常相关(p <0.001)。我们没有发现三组肝外胆管狭窄的位置(p = 0.220)或长度(p = 0.703),胆管狭窄的增强(p = 0.033),上腹部淋巴结肿大或腹膜后纤维化之间的统计学意义。虽然当比较所有三组时肝内胆管狭窄的存在在统计学上是显着的,但它对于区分ISD和PSC没有用。结论。胆管中存在连续性而非跳跃性疾病,胆囊受累以及单壁胆总管厚度大于2.5 mm的存在支持了ISD优于PSC的诊断。 ISD和PSC不能根据胆总管狭窄的位置和长度来区分。

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