Recurrent deep-vein thrombosis based on homozygous factor V Leiden mutation acquired after liver transplantation

Liver Transpl. 2003 Aug;9(8):870-3. doi: 10.1053/jlts.2003.50136.

Abstract

Several genetic liver diseases can be treated by liver transplantation (LT). However, some genetic defects also may be acquired by this procedure. We describe a patient who developed recurrent deep-vein thromboses after LT for hepatitis C virus-associated hepatocellular carcinoma on the basis of a homozygous Leiden mutation of the factor V gene in the donor liver. Liver donors with a history of venous thrombosis should be screened for the presence of activated protein C (APC) resistance. In addition, we recommend looking for APC resistance in liver recipients who develop venous thromboembolic disease in the post-LT course. Molecular analysis of donor tissue may be necessary to make a definite diagnosis of factor V Leiden mutation in these patients. As a consequence, intensified postoperative thromboprophylaxis or lifelong anticoagulant therapy may be necessary if this thrombophilic gene defect is detected.

Publication types

  • Case Reports

MeSH terms

  • Activated Protein C Resistance / etiology
  • Anticoagulants / therapeutic use
  • Factor V / genetics*
  • Female
  • Humans
  • Liver Transplantation / adverse effects*
  • Living Donors
  • Middle Aged
  • Phenprocoumon / therapeutic use
  • Recurrence
  • Venous Thrombosis / etiology*

Substances

  • Anticoagulants
  • factor V Leiden
  • Factor V
  • Phenprocoumon