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
[1]  
Alhenc-Gelas M, 1999, THROMB HAEMOSTASIS, V81, P193
[2]  
BELL G, 1991, P NATL ACAD SCI USA, V78, P5759
[3]   A factor V genetic component differing from factor V R506Q contributes to the activated protein C resistance phenotype [J].
Bernardi, F ;
Faioni, EM ;
Castoldi, E ;
Lunghi, B ;
Castaman, G ;
Sacchi, E ;
Mannucci, PM .
BLOOD, 1997, 90 (04) :1552-1557
[4]   MUTATION IN BLOOD-COAGULATION FACTOR-V ASSOCIATED WITH RESISTANCE TO ACTIVATED PROTEIN-C [J].
BERTINA, RM ;
KOELEMAN, BPC ;
KOSTER, T ;
ROSENDAAL, FR ;
DIRVEN, RJ ;
DERONDE, H ;
VANDERVELDEN, PA ;
REITSMA, PH .
NATURE, 1994, 369 (6475) :64-67
[5]   Secretable human platelet-derived factor V originates from the plasma pool [J].
Camire, RM ;
Pollak, ES ;
Kaushansky, K ;
Tracy, PB .
BLOOD, 1998, 92 (09) :3035-3041
[6]   ORTHOTOPIC LIVER-TRANSPLANTATION WITH PRESERVATION OF THE CAVAL AND PORTAL FLOWS - TECHNIQUE AND RESULTS IN 62 CASES [J].
CHERQUI, D ;
LAUZET, JY ;
ROTMAN, N ;
DUVOUX, C ;
DHUMEAUX, D ;
JULIEN, M ;
FAGNIEZ, PL .
TRANSPLANTATION, 1994, 58 (07) :793-796
[7]   BIOSYNTHESIS OF FACTOR-V IN ISOLATED GUINEA-PIG MEGAKARYOCYTES [J].
CHIU, HC ;
SCHICK, PK ;
COLMAN, RW .
JOURNAL OF CLINICAL INVESTIGATION, 1985, 75 (02) :339-346
[8]  
DALHBACK B, 1993, P NATL ACAD SCI USA, V90, P1004
[9]  
De Mitrio V, 1999, BLOOD COAGUL FIBRIN, V10, P211
[10]   SOURCES OF DNA FOR DETECTING B-CELL MONOCLONALITY USING PCR [J].
DISS, T ;
PAN, L ;
PENG, H ;
WOTHERSPOON, AC ;
ISAACSON, PG .
JOURNAL OF CLINICAL PATHOLOGY, 1994, 47 (06) :493-496