In addition to classic vascular insults such as inflammation, trauma,
malignancy, and surgery, a number of hereditary coagulation defects pr
edispose patients to a wide array of thrombotic complications. A novel
genetic defect in factor V allowing for resistance to its cleavage by
activated protein C has recently been implicated in a significant num
ber of cases of familial thrombophilia. A brief case report and review
of the literature is presented to familiarize surgeons to this import
ant and quite frequent cause of hypercoagulability.