Portal Vein Thrombosis in a Patient with Hereditary Antithrombin Deficiency

Intern Med. 2019 Jun 15;58(12):1733-1737. doi: 10.2169/internalmedicine.2295-18. Epub 2019 Feb 25.

Abstract

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.

Keywords: anticoagulation therapy; antithrombin deficiency; portal vein thrombosis.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Antithrombin III Deficiency / complications*
  • Humans
  • Male
  • Portal Vein*
  • Venous Thrombosis / drug therapy
  • Venous Thrombosis / etiology*