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Intern Med ; 58(12): 1733-1737, 2019 Jun 15.
Artículo en Inglés | MEDLINE | ID: mdl-30799362

RESUMEN

Portal vein thrombosis (PVT) has been reported in many patients with and without liver cirrhosis. The portal vein is a rare site of thrombosis, and various conditions can predispose an individual to PVT. Among those conditions, hereditary thrombophilia has been increasingly reported recently. We herein report the case of a non-cirrhotic 30-year-old man who developed acute PVT with hereditary antithrombin deficiency. Antithrombin (AT) replacement therapy was required along with heparin. Given our experience with this case, we believe that a screening test for prothrombotic disorders, such as AT deficiency, should be considered in cases of PVT.


Asunto(s)
Deficiencia de Antitrombina III/complicaciones , Vena Porta , Trombosis de la Vena/etiología , Adulto , Humanos , Masculino , Trombosis de la Vena/tratamiento farmacológico
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