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首页> 外文期刊>Journal of visceral surgery >Portal biliopathy as a complication of extrahepatic portal hypertension: etiology, presentation and management.
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Portal biliopathy as a complication of extrahepatic portal hypertension: etiology, presentation and management.

机译:门静脉胆病作为肝外门静脉高压症的并发症:病因,表现和治疗。

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摘要

Portal biliopathy (PB) refers to the biliary abnormalities of the biliary ducts observed in patients with extrahepatic portal hypertension. Although majority of patients are asymptomatic, approximately 20% of these patients present with biliary symptoms (pain, pruritus, jaundice, cholangitis). The pathogenesis of PB is uncertain but compression by dilated veins into or around common bile duct may play the main role. CT-scan, MR cholangiopancreatography with MR portography should be the initial investigations in the evaluation of PB. Treatment is limited to symptomatic cases and is dictated by clinical manifestations and complications of the disease. Treatment of PB could be done by endoscopy (sphincterotomy, stone extraction or biliary stenting of the common bile duct) or surgery (definitive decompression by porto-systemic shunt followed by bilioenteric anastomosis, if necessary). This review describes pathogenesis, clinical features, investigation and management of portal biliopathy.
机译:门静脉胆病(PB)是指在肝外门静脉高压症患者中观察到的胆管异常。尽管大多数患者无症状,但这些患者中约有20%出现胆道症状(疼痛,瘙痒,黄疸,胆管炎)。 PB的发病机制尚不确定,但扩张的静脉压入胆总管或胆总管周围可能起主要作用。 CT扫描,MR胰胆管造影和MR门静脉造影应是评估PB的初步研究。治疗仅限于有症状的病例,并由疾病的临床表现和并发症决定。 PB的治疗可以通过内窥镜检查(括约肌切开术,结石摘除或胆总管胆道支架置入术)或手术(必要时通过门体系统分流再行胆肠吻合术进行明确减压)进行。这篇综述描述了门静脉胆病的发病机制,临床特征,研究和治疗。

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