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

  • Marc Willems
  • Martina Sterneck
  • Florian Langer
  • Roman Jung
  • Munif Haddad
  • Christian Hagel
  • Robert Kuetemeier
  • Barbara Eifrig
  • Dieter Broering
  • Lutz Fischer
  • Xavier Rogiers

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.

Bibliografische Daten

OriginalspracheDeutsch
Aufsatznummer8
ISSN1527-6465
StatusVeröffentlicht - 2003
pubmed 12884202