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10.4254/wjh.v7.i19.2229

http://scihub22266oqcxt.onion/10.4254/wjh.v7.i19.2229
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C4561778!4561778!26380049
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suck abstract from ncbi


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pmid26380049      World+J+Hepatol 2015 ; 7 (19): 2229-36
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  • Liver transplantation in a patient with primary antiphospholipid syndrome and Budd-Chiari syndrome #MMPMID26380049
  • Reshetnyak TM; Seredavkina NV; Satybaldyeva MA; Nasonov EL; Reshetnyak VI
  • World J Hepatol 2015[Sep]; 7 (19): 2229-36 PMID26380049show ga
  • The antiphospholipid syndrome (APS) is an acquired thrombophilic disorder in which autoantibodies are produced to a variety of phospholipids determinants of cell membranes or phospholipid binding proteins. There are few reports about association between antiphospholipid antibodies and development of Budd-Chiari syndrome (BCS). We report the case of BCS development in young Russian male with primary APS. The patient underwent orthotopic liver transplantation on August 26, 2012. At present time his state is good, the blood flow in the liver restored and its function is not impaired. We report about the first time the successful use of dabigatran etexilate for prolonged anticoagulation therapy in APS patient with BCS. In addition patient is managed with immunosuppressive drugs.
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