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布加综合征继发于真性红细胞增多症。病例报告。

Budd-Chiari syndrome secondary to polycythemia vera. A case report.

机构信息

Third Medical Clinic, Radiology Department, University of Medicine and Pharmacy, Croitorilor Str., 19-21, Cluj-Napoca, Romania.

出版信息

J Gastrointestin Liver Dis. 2009 Sep;18(3):363-6.

PMID:19795034
Abstract

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.

摘要

布加综合征仍然是肝病学家在病因和最有效治疗方面面临的挑战。真性红细胞增多症被认为是导致布加综合征的最常见疾病(占 10-40%的病例)。我们报告了一位 34 岁的产后患者,因右上腹疼痛和乏力入院。实验室数据、腹部超声和血管 MRI 均提示布加综合征,但在血液科诊断为真性红细胞增多症,导致了肝脏疾病。

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1
Budd-Chiari syndrome secondary to polycythemia vera. A case report.布加综合征继发于真性红细胞增多症。病例报告。
J Gastrointestin Liver Dis. 2009 Sep;18(3):363-6.
2
[The Budd-Chiari syndrome as the first manifestation of polycythemia vera].[布加综合征作为真性红细胞增多症的首发表现]
An Med Interna. 1991 Jan;8(1):27-9.
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Early medical treatment is life saving in acute Budd-Chiari due to polycythemia vera.早期医学治疗对于真性红细胞增多症所致的急性布加综合征是挽救生命的。
Hepatogastroenterology. 2003 Mar-Apr;50(50):512-4.
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[Budd-Chiari syndrome with fatal outcome in a patient with polycythemia vera and antiphospholipid antibody syndrome].[真性红细胞增多症和抗磷脂抗体综合征患者发生的布加综合征并导致致命结局]
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Budd--Chiari syndrome complicating polycythaemia vera. A case report.真性红细胞增多症并发布加综合征。病例报告。
Ghana Med J. 1975 Sep;14(3):243-4.
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JAK2V617F mutation in a 9-year-old girl with polycythemia vera and Budd-Chiari syndrome: a case report.一名患有真性红细胞增多症和布加综合征的9岁女孩的JAK2V617F突变:病例报告
J Pediatr Hematol Oncol. 2012 Apr;34(3):243-4. doi: 10.1097/MPH.0b013e31820150bf.
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Familial polycythemia vera with Budd-Chiari syndrome in childhood.儿童期伴有布加综合征的家族性真性红细胞增多症
Br J Haematol. 2003 Oct;123(2):346-52. doi: 10.1046/j.1365-2141.2003.04591.x.
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[Budd-Chiari syndrome in the course of polycythemia rubra vera. Presentation of a clinical case].[真性红细胞增多症病程中的布加综合征。1例临床病例报告]
Minerva Med. 1979 Dec 1;70(54):3719-24.
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[Post-hepatic venous occlusion (Budd-Chiari syndrome) - diagnosis illustrated by case reports].[肝后静脉闭塞(布加综合征)——病例报告说明诊断]
Ugeskr Laeger. 1981 Sep 14;143(38):2439-41.
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[Oral contraceptives and blood diseases are the most common causes of Budd-Chiari syndrome].口服避孕药和血液疾病是布加综合征最常见的病因。
Lakartidningen. 1989 Nov 15;86(46):4002-8.