Activated protein C resistance acquired through liver transplantation and associated with recurrent venous thrombosis

被引:25
作者
Leroy-Matheron, C
Duvoux, C
Van Nhieu, JT
Leroy, K
Cherqui, D
Gouault-Heilmann, M
机构
[1] CHU Henri Mondor, Serv Hematol Biol, Unite Hemostase & Thrombose, AP HP, F-94010 Creteil, France
[2] CHU Henri Mondor, Serv Hepatogastroenterol, AP HP, Creteil, France
[3] CHU Henri Mondor, AP HP, Dept Pathol, Creteil, France
[4] CHU Henri Mondor, AP HP, Serv Chirurg Digest, Creteil, France
关键词
liver transplantation; activated protein C resistance; FV Leiden;
D O I
10.1016/S0168-8278(03)00054-0
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
We report a new case of recurrent, extra-hepatic, deep vein thrombosis occurring after orthotopic liver transplantation for hepatocellular carcinoma complicating 'mixed' alcoholic and post-hepatitic C cirrhosis. Coagulation tests showed activated protein C resistance. The patient's genomic DNA was negative for the factor V Leiden mutation. Analysis of the grafted liver DNA showed that the donor was a heterozygous carrier of the factor V Leiden mutation and that the recipient's activated protein C resistance was acquired through the transplantation. Screening of candidate liver donors for a prothrombotic tendency is controversial. However, this case suggests that patients who develop venous thrombosis after liver transplantation should be screened for thrombophilic abnormalities, bearing in mind that genetic abnormalities which do not affect clotting test results, such as the G20210A mutation in the factor 11 gene, can only be diagnosed by testing the donor or graft. (C) 2003 European Association for the Study of the Liver. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:866 / 869
页数:4
相关论文
共 30 条
[11]   Coinheritance of the HR2 haplotype in the factor V gene confers an increased risk of venous thromboembolism to carriers of factor V R506Q (Factor V leiden) [J].
Faioni, EM ;
Franchi, F ;
Bucciarelli, P ;
Margaglione, M ;
De Stefano, V ;
Castaman, G ;
Finazzi, G ;
Mannucci, PM .
BLOOD, 1999, 94 (09) :3062-3066
[12]   A RAPID SCREENING METHOD FOR THE FACTOR-V ARG506-]GLN MUTATION [J].
GANDRILLE, S ;
ALHENCGELAS, M ;
AIACH, M .
BLOOD COAGULATION & FIBRINOLYSIS, 1995, 6 (03) :245-248
[13]   CELLULAR AND MOLECULAR REGULATION OF FACTOR-V EXPRESSION IN HUMAN MEGAKARYOCYTES [J].
GEWIRTZ, AM ;
SHAPIRO, C ;
SHEN, YM ;
BOYD, R ;
COLMAN, RW .
JOURNAL OF CELLULAR PHYSIOLOGY, 1992, 153 (02) :277-287
[14]  
GEWIRTZ AM, 1986, BLOOD, V67, P1639
[15]  
Gillis S, 2000, HAEMOSTASIS, V30, P316
[16]  
GRIFFIN JH, 1993, BLOOD, V82, P1989
[17]   Donor factor V Leiden mutation and vascular thrombosis following liver transplantation [J].
Hirshfield, G ;
Collier, JD ;
Brown, K ;
Taylor, C ;
Frick, T ;
Baglin, TP ;
Alexander, GJM .
LIVER TRANSPLANTATION AND SURGERY, 1998, 4 (01) :58-61
[18]   CHARACTERIZATION OF THE MOLECULAR DEFECT IN FACTOR V-R506Q [J].
KALAFATIS, M ;
BERTINA, RM ;
RAND, MD ;
MANN, KG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (08) :4053-4057
[19]  
KALAFATIS M, 1994, J BIOL CHEM, V269, P31869
[20]   VENOUS THROMBOSIS DUE TO POOR ANTICOAGULANT RESPONSE TO ACTIVATED PROTEIN-C - LEIDEN THROMBOPHILIA STUDY [J].
KOSTER, T ;
ROSENDAAL, FR ;
DERONDE, H ;
BRIET, E ;
VANDENBROUCKE, JP ;
BERTINA, RM .
LANCET, 1993, 342 (8886-7) :1503-1506