Literature DB >> 26176558

Budd-Chiari syndrome complicating essential thrombocythemia in an adolescent: favorable outcome of TIPS procedure.

Azza Abdel-Gawad Tantawy1, Amira Abdel-Monem Adly, Yasmine Ibrahim Elhenawy.   

Abstract

Budd-Chiari syndrome (BCS) is a liver disorder characterized by hepatic venous outflow obstruction, mainly resulting from thrombosis of the terminal part of the hepatic veins or the inferior vena cava. It causes hepatic congestion, ascites, portal hypertension, and collateral circulation between the obstructed and contiguous patent venous territories. BCS is reported complicating myeloproliferative disorders, as well other prothrombotic events. Essential thrombocythemia is one of the most frequent myeloproliferative disorders that cause BCS, and in some cases, it may be the initial presentation. Many treatment options have been proposed for BCS, routine anticoagulation therapy being recommended as the first therapeutic approach.

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Year:  2015        PMID: 26176558     DOI: 10.1097/MBC.0000000000000325

Source DB:  PubMed          Journal:  Blood Coagul Fibrinolysis        ISSN: 0957-5235            Impact factor:   1.276


  1 in total

1.  MPL-Positive Essential Thrombocytosis Presenting as Budd-Chiari Syndrome in a Middle-Aged Woman with an Initially Normal Platelet Count.

Authors:  Mohammad Ammad Ud Din; Hania Liaqat; Muhammad Osama
Journal:  Eur J Case Rep Intern Med       Date:  2021-12-17
  1 in total

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