Current guidelines for diagnosis and management of hepatic involvement in hereditary hemorrhagic teleangiectasia
作者机构:Department of Medical and Surgical SciencesUniversity of BolognaBologna 40138Italy Department of Internal MedicineOspedale per gli Infermi di FaenzaFaenza 48018Italy Division of Internal MedicineHepatobiliary and Immunoallergic DiseasesIRCCS Azienda Ospedaliero-Universitaria di BolognaBologna 40138Italy
出 版 物:《World Journal of Hepatology》 (世界肝病学杂志(英文版)(电子版))
年 卷 期:2023年第15卷第5期
页 面:675-687页
学科分类:1002[医学-临床医学] 100201[医学-内科学(含:心血管病、血液病、呼吸系病、消化系病、内分泌与代谢病、肾病、风湿病、传染病)] 10[医学]
主 题:involvement diagnosis hemorrhagic
摘 要:Hereditary hemorrhagic teleangiectasia(HHT),also known as Rendu-Osler-Weber syndrome,is the most common cause of hepatic vascular malformations in *** vascular shunts(arteriovenous,arterioportal or portovenous)lead to different clinical *** though no hepatic-related symptoms are reported in the majority of cases,the severity of liver disease could lead to refractory medical conditions,in some cases requiring liver *** aim of this manuscript is to provide an updated overview of the current evidence regarding the diagnosis and treatment of HHT liver involvement and liver-related complications.