首页|期刊导航|中国中西医结合外科杂志|磁共振胰胆管造影对胰胆管汇合异常与胰胆管高位汇合在胆道癌中的危险因素预测作用

磁共振胰胆管造影对胰胆管汇合异常与胰胆管高位汇合在胆道癌中的危险因素预测作用OA

MRCP predicts the distribution of benign and malignant biliary lesions in pancreaticobiliary maljunction and high confluence of pancreaticobiliary ducts,as well as the risk factors for biliary tract cancer

中文摘要英文摘要

目的:探讨胰胆管汇合异常(PBM)与胰胆管高位汇合(HCPBD)在胆道良恶性病变中分布的特征,并分析其与胆道癌发病相关的预测因素.方法:回顾性分析2021年1月-2024年5月天津市南开医院收治的4321例胆道术后患者的资料,其中良性胆道病变4065例,胆囊癌98例,胆管癌158例.分析所有患者的磁共振胰胆管造影(MRCP)影像资料与临床资料,分析PBM与HCPBD在胆道良恶性病变的分布特征,并采用多因素Logistic回归分析胆道癌的独立影响因素,构建列线图预测模型,通过受试者工作曲线(ROC)、校正曲线分析各指标的预测价值.结果:胆道癌患者中PBM与HCPBD的检出率均显著高于良性胆道病变患者(P<0.001).PBM在胆囊癌中检出率最高(16.3%,16/98).合并胆道癌的PBM和HCPBD患者的年龄、共同通道长度、胆总管扩张比例高于未合并胆道癌的PBM和HCPBD患者,差异有统计学意义(P<0.001),且主要影响女性.多因素Logistic回归分析显示年龄(OR=1.070,P=0.004)、胆道是否扩张(OR=5.472,P=0.004)及共同管道长度(OR=1.161,P=0.012)是胆道癌的独立预测因素,将3项风险因素联合构建列线图预测模型,ROC曲线分析显示列线图模型预测胆道癌的AUC为0.92(95%CI:0.85~0.98).校正曲线示模型预测率和实际概率具有较高的一致性.结论:PBM、HCPBD与胆道癌发生密切相关,尤其在胆囊癌中更常见.年龄、胆道扩张及共同通道长度是预测PBM与HCPBD患者发生胆道癌的独立影响因素,基于以上因素构建的列线图模型可为识别高危患者,提高诊断准确性.

Objective To explore the distribution characteristics of pancreaticobiliary maljunction(PBM)and high confluence of pancreaticobiliary ducts(HCPBD)in benign and malignant biliary lesions and analyze the predictive factors related to the incidence of biliary tract cancer.Methods A retrospective analysis was conducted on 4321 patients after biliary tract surgery admitted to Nankai Hospital in Tianjin from January 2021 to May 2024.Among them,there were 4065 cases of benign biliary tract lesions,98 cases of gallbladder cancer,and 158 cases of cholangiocarcinoma.Analysis of magnetic resonance imaging pancreatic and all patients magnetic resonance cholangiopancreatography(MRCP)image data and clinical data,analysis of PBM and HCPBD in biliary distribution characteristics of benign and malignant lesions.Multivariate logistic regression was used to analyze the independent influencing factors of biliary tract cancer,and a nomogram prediction model was constructed.The predictive value of each index was analyzed through the receiver operating characteristic curve(ROC)and correction curve.Results The detection rates of PBM and HCPBD in patients with biliary tract cancer were significantly higher than those in the benign lesion group(P<0.001).PBM has the highest detection rate(16.3%,16/98)in gallbladder cancer.The age,common channel length and the proportion of common bile duct dilation in PBM and HCPBD patients with biliary tract cancer were higher than those in PBM and HCPBD patients without biliary tract cancer,and the differences were statistically significant(P<0.001),mainly affecting females.Multivariate Logistic regression analysis showed that age(OR=1.070,P=0.004),biliary dilation(OR=5.472,P=0.004),and common duct length(OR=1.161,P=0.012)were independent predictors of biliary tract cancer.The three risks were combined to construct a nomogram prediction model.ROC curve analysis showed that the AUC of the nomogram model for predicting biliary tract cancer was 0.92(95%CI:0.85-0.98).The correction curve indicates that the model's prediction rate has a high consistency with the actual probability.Conclusion PBM and HCPBD are closely related to the occurrence of biliary tract cancer,especially being more common in gallbladder cancer.Age,whether the biliary tract is dilated and the length of the common channel are independent risk factors for predicting biliary tract cancer in patients with PBM and HCPBD.The nomogram model constructed based on the above factors can help identify high-risk patients and improve diagnostic accuracy.

高峰;宫琰;翁婷婷;孙雨萌;张翔

天津医科大学附属南开医院医学影像科||天津市中西医结合急腹症研究所(天津 300100)天津医科大学附属南开医院医学影像科||天津市中西医结合急腹症研究所(天津 300100)天津医科大学附属南开医院医学影像科||天津市中西医结合急腹症研究所(天津 300100)天津医科大学附属南开医院医学影像科||天津市中西医结合急腹症研究所(天津 300100)天津医科大学附属南开医院医学影像科||天津市中西医结合急腹症研究所(天津 300100)

医药卫生

胰胆管汇合异常胰胆管高位汇合胆道癌共同通道长度胆总管扩张危险因素

Pancreaticobiliary maljunctionhigh confluence of pancreaticobiliarybiliary cancercommon channel lengthdilated common bile ductrisk factors

《中国中西医结合外科杂志》 2026 (3)

355-360,6

天津市教委科研计划项目(自然科学)(2024KJ244)

10.3969/j.issn.1007-6948.2026.03.010

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