Presence of ADAMTS13 activity in a patient with metastatic cancer and thrombotic microangiopathy

被引:17
作者
Forman, RB
Benkel, SA
Novik, Y
Tsai, HM
机构
[1] Montefiore Med Ctr, Albert Einstein Coll Med, Div Hematol, Bronx, NY 10467 USA
[2] Beth Israel Med Ctr, New York, NY 10003 USA
关键词
ADAMTS13; metastatic cancer; microangiopathic hemolysis; thrombocytopenia; thrombotic thrombocytopenic purpura;
D O I
10.1159/000069291
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Patients with metastatic cancers occasionally present with microangiopathic hemolysis and thrombocytopenia. A patient with metastatic adenocarcinoma of the colon and microangiopathic hemolysis was treated with plasma exchange for a presumptive diagnosis of thrombotic thrombocytopenic purpura (TTP). However, her condition continued to deteriorate and a determination of ADAMTS13 activity revealed that she did not have TTP. Despite similarity in clinical manifestation, microangiopathic hemolysis in patients with metastatic cancers may not be caused by ADAMTS13 deficiency and the role of plasma exchange in such patients should be re-evaluated. Copyright (C) 2003 S. Karger AG, Basel.
引用
收藏
页码:150 / 152
页数:3
相关论文
共 16 条
[1]  
Bell WR, 1997, SEMIN HEMATOL, V34, P134
[2]   IMPROVED SURVIVAL IN THROMBOTIC THROMBOCYTOPENIC PURPURA HEMOLYTIC UREMIC SYNDROME - CLINICAL-EXPERIENCE IN 108 PATIENTS [J].
BELL, WR ;
BRAINE, HG ;
NESS, PM ;
KICKLER, TS .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 325 (06) :398-403
[3]   Microangiopathic haemolytic anaemia in metastasizing malignant tumours is not associated with a severe deficiency of the von Willebrand factor-cleaving protease [J].
Fontana, S ;
Gerritsen, HE ;
Hovinga, JK ;
Furlan, M ;
Lämmle, B .
BRITISH JOURNAL OF HAEMATOLOGY, 2001, 113 (01) :100-102
[4]   Von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome [J].
Furlan, M ;
Robles, R ;
Galbusera, M ;
Remuzzi, G ;
Kyrle, PA ;
Brenner, B ;
Krause, M ;
Scharrer, I ;
Aumann, V ;
Mittler, U ;
Solenthaler, M ;
Lämmle, B .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (22) :1578-1584
[5]   Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura [J].
Levy, GG ;
Nichols, WC ;
Lian, EC ;
Foroud, T ;
McClintick, JN ;
McGee, BM ;
Yang, AY ;
Siemieniak, DR ;
Stark, KR ;
Gruppo, R ;
Sarode, R ;
Shurin, SB ;
Chandrasekaran, V ;
Stabler, SP ;
Sabio, H ;
Bouhassira, EE ;
Upshaw, JD ;
Ginsburg, D ;
Tsai, HM .
NATURE, 2001, 413 (6855) :488-494
[6]  
Moschcowitz E., 1924, PROC N PATHOL SOC, V24, P21
[7]  
Oleksowicz L, 1999, CANCER RES, V59, P2244
[8]   Unintentional platelet removal by plasmapheresis [J].
Perdue, JJ ;
Chandler, LK ;
Vesely, SK ;
Duvall, DS ;
Gilcher, RO ;
Smith, JW ;
George, JN .
JOURNAL OF CLINICAL APHERESIS, 2001, 16 (02) :55-60
[9]   COMPARISON OF PLASMA-EXCHANGE WITH PLASMA INFUSION IN THE TREATMENT OF THROMBOTIC THROMBOCYTOPENIC PURPURA [J].
ROCK, GA ;
SHUMAK, KH ;
BUSKARD, NA ;
BLANCHETTE, VS ;
KELTON, JG ;
NAIR, RC ;
SPASOFF, RA .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 325 (06) :393-397
[10]   LATE RELAPSES IN PATIENTS SUCCESSFULLY TREATED FOR THROMBOTIC THROMBOCYTOPENIC PURPURA [J].
SHUMAK, KH ;
ROCK, GA ;
NAIR, RC ;
ADAMS, G ;
BENNY, B ;
BUSKARD, NA ;
CAPLAN, S ;
CARD, R ;
CLARK, WF ;
FORD, P ;
FREEDMAN, J ;
GORDON, P ;
GORELICK, M ;
KELTON, J ;
KLASSEN, J ;
LEBLOND, P ;
LEPINEMARTIN, M ;
MCBRIDE, J ;
MONTE, M ;
RAYNER, H ;
SHORE, T ;
STERNBACH, M ;
SUTTON, DMC ;
JONES, JV .
ANNALS OF INTERNAL MEDICINE, 1995, 122 (08) :569-572