1 Department of Medical Imaging, Abdominal Imaging, University Health Network, Mount Sinai Hospital and Women's College Hospital, University of Toronto, 610 University Ave, Toronto, ON M5G 2M9, Canada.
AJR Am J Roentgenol. 2014 Mar;202(3):536-43. doi: 10.2214/AJR.12.10360.
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.
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.
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.
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.
本研究旨在对 IgG4 相关系统性疾病(ISD,也称自身免疫性胰腺炎)、原发性硬化性胆管炎(PSC)和自身免疫性肝病(自身免疫性肝炎和原发性胆汁性肝硬化)的胆管疾病形态模式进行回顾性 MRI 对比分析。
本研究纳入了 162 例连续登记的患者(ISD 组 47 例,PSC 组 73 例,自身免疫性肝病组 42 例)。两位腹部放射科医生进行了共识性的回顾性 MRI 图像审查。对胆管、肝脏、胰腺和其他器官的影像学表现进行分析,以确定疾病模式。
ISD 与肝内外胆管连续性增厚(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)相关。ISD 患者胆总管壁厚度的严重程度差异有统计学意义(p<0.001)。ISD 组平均单层壁厚度为 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(p<0.001)相关。三组间肝外胆管狭窄的位置(p=0.220)或长度(p=0.703)、胆管狭窄强化(p=0.033)、上腹部淋巴结肿大或腹膜后纤维化差异均无统计学意义。虽然三组比较时均有肝内胆管狭窄,但对 ISD 与 PSC 的鉴别并无帮助。
胆管存在连续性而非跳跃性疾病、胆囊受累、胆总管单层厚度大于 2.5mm 提示 ISD 的诊断优于 PSC。基于胆总管狭窄的位置和长度,无法对 ISD 和 PSC 进行区分。