Thromb Haemost 1988; 60(01): 013-017
DOI: 10.1055/s-0038-1647625
Original Article
Schattauer GmbH Stuttgart

Further Evidence of von Willebrand Factor Involvement in Thrombotic Thrombocytopenia Purpura

Autoren

  • J Chediak

    The Joint Section of Hematology/Oncology, Department of Medicine, Michael Reese Hospital and the University of Chicago Hospitals, Chicago, IL, USA
  • J Eldridge

    The Joint Section of Hematology/Oncology, Department of Medicine, Michael Reese Hospital and the University of Chicago Hospitals, Chicago, IL, USA
  • F Bergmann

    The Joint Section of Hematology/Oncology, Department of Medicine, Michael Reese Hospital and the University of Chicago Hospitals, Chicago, IL, USA
  • D Sobel

    The Joint Section of Hematology/Oncology, Department of Medicine, Michael Reese Hospital and the University of Chicago Hospitals, Chicago, IL, USA
  • J Baron

    The Joint Section of Hematology/Oncology, Department of Medicine, Michael Reese Hospital and the University of Chicago Hospitals, Chicago, IL, USA
  • B Maxey

    The Joint Section of Hematology/Oncology, Department of Medicine, Michael Reese Hospital and the University of Chicago Hospitals, Chicago, IL, USA
  • M C Telfer

    The Joint Section of Hematology/Oncology, Department of Medicine, Michael Reese Hospital and the University of Chicago Hospitals, Chicago, IL, USA
Weitere Informationen

Publikationsverlauf

Received 29. September 1987

Accepted after revision 10. März 1988

Publikationsdatum:
30. Juni 2018 (online)

Summary

Fourteen patients diagnosed as having thrombotic thrombocytopenia purpura (TTP) were studied. Those who survived have been followed during a 1 to 7 year period. The clinical diagnosis was based on changing neurological findings, thrombocytopenia and evidence of microangiopathic hemolytic anemia. Laboratory tests included the determination of von Willebrand factor antigen (VWF:Ag), ristocetin cofactor (RiCof) and the electrophoretic mobility of von Willebrand factor (CIE VWF:Ag). The ratio of RiCof to VWF:Ag was then calculated. Control individuals included healthy subjects and patients with thrombocytopenia of several etiologies. Statistical differences between the values of RiCof, the ratio of RiCof : VWF: Ag and the CIE of VWF: Ag were found for samples comparing active disease and remission phase. The recovery from thrombocytopenia paralleled the correction of abnormal parameters. Similarly, significant differences were found when above parameters were compared between thrombocytopenia of TTP with other thrombocytopenic states. We suggest that these abnormal tests could be useful in distinguishing TTP from other disorders, and may have prognostic significance in patients already diagnosed as having TTP.