Budd-Chiari syndrome: current perspectives and controversies

被引:2
作者
Liu, L. [1 ]
Qi, X. -S. [1 ,2 ]
Zhao, Y. [1 ]
Chen, H. [1 ]
Meng, X. -C. [1 ]
Han, G. -H. [1 ]
机构
[1] Fourth Mil Med Univ, Xijing Hosp Digest Dis, Dept Liver Dis & Digest Intervent Radiol, Xian, Peoples R China
[2] Gen Hosp Shenyang Mil Area, Dept Gastroenterol, Shenyang, Peoples R China
基金
中国国家自然科学基金;
关键词
Budd-Chiari syndrome; Etiology; Diagnosis; Treatment; review; PORTAL-VEIN THROMBOSIS; PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA; FACTOR-V-LEIDEN; INTRAHEPATIC PORTOSYSTEMIC SHUNT; SINGLE-CENTER EXPERIENCE; CHINESE PATIENTS; JAK2V617F MUTATION; BEHCETS-DISEASE; MYELOPROLIFERATIVE NEOPLASMS; ENDOVASCULAR TREATMENT;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Budd-Chiari syndrome (BCS) is a rare disorder caused by hepatic venous outflow obstruction with a wide spectrum of etiologies. Clinical manifestations are so heterogeneous that the diagnosis should be considered in any patients with acute or chronic liver disease. Therapeutic modalities for BCS have improved dramatically during the last few years. The concept of a step-wise treatment strategy has been established, including anticoagulation, thrombolysis, percutaneous recanalization, transjugular intrahepatic portosystemic shunt, surgery and liver transplantation. However, this strategy is primarily based on experts' opinions and retrospective case series, rather than prospective randomized trials. Furthermore, an earlier use of TIPS has been proposed in selected cases because of a relatively high mortality from BCS patients who underwent medical therapy alone. Herein, we review the advances in the classification, etiology, clinical presentation, diagnosis and treatment of BCS.
引用
收藏
页码:3273 / 3281
页数:9
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