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[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]

[Budd-Chiari syndrome in the course of polycythemia rubra vera. Presentation of a clinical case].

作者信息

Altomonte L, Mingrone G, Gattini G, Pepe M, Magarò M

出版信息

Minerva Med. 1979 Dec 1;70(54):3719-24.

PMID:523003
Abstract

An unusual case of Budd-Chiari syndrome during erythraemia is presented. Acute thrombosis of the suprahepatic veins became chronic with progressive improvement, shown clinically and radiologically in the form of partial recanalisation of thromboses of these veins and the porta. The pathogenetic relationship between polycythaemia and the Budd-Chiari syndrome is also discussed.

摘要

本文报告了一例真性红细胞增多症并发布加综合征的罕见病例。肝上静脉急性血栓形成转为慢性,病情逐渐改善,临床及影像学表现为这些静脉及肝门血栓部分再通。文中还讨论了红细胞增多症与布加综合征之间的发病机制关系。

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1
[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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[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]
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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。
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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。
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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
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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。
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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。
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Use of transjugular intrahepatic portosystemic shunt as a bridge to transplantation in fulminant hepatic failure due to Budd-Chiari syndrome.经颈静脉肝内门体分流术作为布加综合征所致暴发性肝衰竭患者肝移植过渡治疗的应用
Am J Gastroenterol. 1997 Dec;92(12):2304-6.
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Budd-Chiari syndrome as the first manifestation of polycythemia vera in young women with inherited thrombophilic state: an aggressive form of myeloproliferative disorder requiring multidisciplinary management.布加综合征作为遗传性易栓症年轻女性真性红细胞增多症的首发表现:一种需要多学科管理的侵袭性骨髓增殖性疾病。
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