De novo hepatic tumors following portocaval shunt for Budd-Chiari syndrome

被引：2

作者：

Braun, F

Nolte, W

Lorf, T

Canelo, R

Sattler, B

Müller, D

Vosshenrich, R

Ramadori, G

Ringe, B

机构：

[1] Klin. fur Transplantationschirurgie, Georg-August-Universität, Göttingen

[2] Abt. fur Gastroenterol. Endokrinol., Georg-August-Universität, Göttingen

[3] Zentrum Pathologie, Georg-August-Universität, Göttingen

[4] Zentrum Radiologie, Georg-August-Universität, Göttingen

[5] Klin. fur Transplantationschirurgie, Georg-August-Universität, Robert-Koch-Straße 40

来源：

CHIRURGISCHE GASTROENTEROLOGIE | 1998年 / 14卷 / 04期

关键词：

Budd-Chiari syndrome; portocaval shunt; focal nodular hyperplasia; atrophic/hypertrophic complex; liver tumors;

D O I：

10.1159/000012515

中图分类号：

R57 [消化系及腹部疾病];

学科分类号：

摘要：

The Budd-Chiari syndrome is one cause of portal hypertension with multiple etiology and different therapeutic interventional strategies. We report on a 23-year-old female patient who developed de novo liver tumors 33 months after portocaval shunting for acute Budd-Chiari syndrome.

引用

页码：318 / 322

页数：5

共 26 条

[1]

Bass N.M., 1996, HEPATOLOGY TXB LIVER, V3rd, P962

[2] BUDD-CHIARI SYNDROME - TECHNICAL, HEMODYNAMIC, AND CLINICAL-RESULTS OF TREATMENT WITH TRANSJUGULAR INTRAHEPATIC PORTOSYSTEMIC SHUNT [J].