Acute hepatic vascular complications

被引:3
|
作者
Ochs, A. [1 ]
机构
[1] Loretto Krankenhaus, Innere Abt, D-79100 Freiburg, Germany
来源
INTERNIST | 2011年 / 52卷 / 07期
关键词
Portal vein; Thrombosis; Budd-Chiari syndrome; Transjugular intrahepatic portosystemic shunt (TIPS); M. Osler Weber Rendu; BUDD-CHIARI-SYNDROME; PORTAL-VEIN THROMBOSIS; INTRAHEPATIC PORTOSYSTEMIC SHUNT; LIVER-TRANSPLANTATION; MARROW TRANSPLANTATION; VENOOCCLUSIVE DISEASE; CIRRHOSIS; INVOLVEMENT; MANAGEMENT; DIAGNOSIS;
D O I
10.1007/s00108-010-2795-y
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Acute hepatic vascular complications are rare. Acute portal vein thrombosis (PVT) and the Budd-Chiari syndrome (BSC) are the leading causes. Coagulopathy and local factors are present in up to 80% of cases. Diagnosis is established by colour-coded Doppler sonography, contrast-enhanced computed tomography or magnetic resonance imaging. Patients with acute PVT present with abdominal pain and disturbed intestinal motility. In the absence of cirrhosis anticoagulation with heparin is established followed by oral anticoagulation. In severe cases, surgical thrombectomy or transjugular thrombolysis with stent shunt may be necessary. Acute or fulminant BCS may require emergency liver transplantation or a transjugular intrahepatic portosystemic stent shunt, if patients present with acute liver failure. Milder cases receive anticoagulation for thrombolysis of occluded hepatic veins. Sinusoidal obstruction syndrome (SOS) is diagnosed after total body irradiation or chemotherapy, the term SOS replacing the former veno-occlusive disease. The treatment of congenital vascular malformations, complications in the setting of OLTX as well as patients with hepatic involvement of hereditary hemorrhagic telangiectasia requires significant expertise in a multidisciplinary approach.
引用
收藏
页码:795 / +
页数:7
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