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Coagulation studies in thrombotic thrombocytopenic purpura, with special reference to von willebrand factor and protein S

 

作者: Hoyu Takahashi,   Wataru Tatewaki,   Tadao Nakamura,   Masaharu Hanano,   Ken Wada,   Akira Shibata,  

 

期刊: American Journal of Hematology  (WILEY Available online 1989)
卷期: Volume 30, issue 1  

页码: 14-21

 

ISSN:0361-8609

 

年代: 1989

 

DOI:10.1002/ajh.2830300104

 

出版商: Wiley Subscription Services, Inc., A Wiley Company

 

关键词: von Willebrand factor multimers;von Willebrand factor fragment;blood coagulation;fibrinolysis;complements

 

数据来源: WILEY

 

摘要:

AbstractThe profile of blood coagulation and fibrinolysis was studied in detail in eight patients with acute thrombotic thrombocytopenic purpura (TTP). In the majority of the patients, fibrinogen, factor XIII, antithrombin III, α2‐plasmin inhibitor, plasminogen, and α2‐macroglobulin were normal, whereas FDP, plasmin‐α2‐plasmin inhibitor complex, and tissuetype plasminogen activator antigen were marginally or moderately elevated. Low fibronectin values were observed in four patients. Protein C and C4b‐binding protein were nearly normal, whereas total protein S and free protein S were reduced in five and six patients, respectively. A positive correlation was found between total protein S and C4 and between free protein S and C3. von Willebrand factor antigen (vWf:Ag) and ristocetin cofactor (RCof) were either normal or elevated, but RCof/vWf:Ag ratio was decreased in seven patients. Crossed immunoelectrophoresis and sodium dodecyl sulfate (SDS)‐agarose gel electrophoresis revealed that the large vWf multimers were either absent from or relatively decreased in all patients except one. In addition, one patient had unusually large vWf multimers, and a low‐molecular‐weight vWf fragment was apparently observed in three patients. These findings indicate that the intravascular generation of thrombin and plasmin was minimal in TTP and suggest that the alterations of the vWf molecule were caused not only by consumption through its participation in platelet thrombus formation but also by accelerated proteolysis. Low protein S values would be related to the immunological abnormalit

 

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