Controversies in the Use of Portal Vein Embolization

被引:70
作者
van Gulik, Thomas M. [1 ]
van den Esschert, Jacomina W. [1 ]
de Graaf, Wilmar [1 ]
van Lienden, Krijn P. [2 ]
Busch, Olivier R. C. [1 ]
Heger, Michal [1 ]
van Delden, Otto M. [2 ]
Lameris, Johan S. [2 ]
Gouma, Dirk J. [1 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Surg, NL-1105 AZ Amsterdam, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, Dept Radiol, NL-1105 AZ Amsterdam, Netherlands
关键词
Portal vein; Embolization; Liver resection; regeneration; hypertrophy;
D O I
10.1159/000184735
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: Portal vein embolization (PVE) has reached worldwide acceptance to increase future remnant liver (FRL) volume before undertaking major liver resection. The aim of this overview is to point out and discuss current controversies in the application of PVE. Methods: Review of literature pertaining to techniques of PVE, complications, tumor proliferation, timing of resection, and hypertrophy response after PVE. Results: Procedure-related complications after PVE include hematoma, hemobilia, overflow of embolization material, and thrombosis of portal vein branch(es) of the non-embolized lobe. Persistence of the embolized, atrophic lobe is usually not harmful. Embolization of the portal branches to segment 4 in addition to embolization of the right portal trunk is controversial and is advised only in selected cases. It remains undecided whether embolization of the portal venous system is more effective in inducing hypertrophy of the FRL than ligation of the portal vein. Accelerated tumor growth after PVE is a major concern and requires consideration of post-PVE chemotherapy. A waiting time of 3 weeks between PVE and liver resection is advised. Post-hepatectomy regeneration is not hampered after preoperative PVE. Conclusion: PVE is a useful preoperative intervention to increase volume and function of the FRL. Further progress awaits clarification of the mechanisms of the hypertrophy response induced by PVE in conjunction with new embolization materials and protective chemotherapy. Copyright (c) 2009 S. Karger AG, Basel
引用
收藏
页码:436 / 444
页数:9
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