Budd-Chiari Syndrome Secondary to Polycythemia Vera. A Case Report

被引：0

作者：

Buzas, Claudia ^{[1
]}

Sparchez, Zeno ^{[1
]}

Cucuianu, Andrei ^{[2
]}

Manole, Simona ^{[3
]}

Lupescu, Ioana ^{[4
]}

Acalovschi, Monica ^{[1
]}

机构：

[1] Univ Med & Pharm, Med Clin 3, Cluj Napoca, Romania

[2] Univ Med & Pharm, Haematol Clin, Cluj Napoca, Romania

[3] Univ Med & Pharm, Dept Radiol, Cluj Napoca, Romania

[4] Clin Inst Fundeni, Dept Radiol, Bucharest, Romania

来源：

JOURNAL OF GASTROINTESTINAL AND LIVER DISEASES | 2009年 / 18卷 / 03期

关键词：

Budd-Chiari syndrome; polycythemia vera; MUTATION; ANGIOGRAPHY; INHIBITOR; DIAGNOSIS; V617F;

D O I：

暂无

中图分类号：

R57 [消化系及腹部疾病];

学科分类号：

摘要：

Budd-Chiari syndrome still represents a challenge for the hepatologist with regard to its causes and its most effective therapy. Polycythemia vera is considered to be the most frequent condition causing the Budd-Chiari syndrome (10-40% of cases). We present a 34-year-old patient in post-partum who was admitted for right upper abdominal quadrant pain and asthenia. Laboratory data, abdominal echography and angioMRI all raised the suspicion of BCS, but it was in the haematological department that polycytemia vera was diagnosed as the cause of the hepatic condition.

引用

页码：363 / 366

页数：4

共 17 条

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