Acquired von Willebrand's disease due to aberrant expression of platelet glycoprotein Ib by marginal zone lymphoma cells

Br J Haematol. 1997 Mar;96(4):850-3. doi: 10.1046/j.1365-2141.1997.d01-2088.x.

Abstract

A 69-year-old woman presented with splenic marginal zone lymphoma associated with acquired von Willebrand's disease (AVWD). Laboratory abnormalities included markedly decreased plasma levels of factor VIII coagulant (C) activity (VIII:C 28%), von Willebrand's factor (VWF) antigen (Ag) (vWF:Ag < 6%), and VWF ristocetin cofactor (RCo) activity (VWF:RCo, < 12%). VWF multimer analysis revealed a severe type II defect. Treatment with cryoprecipitate, high-dose gamma globulin or desmopressin given intravenously was unsuccessful. Clinical bleeding and coagulation abnormalities showed transient improvement after replacement therapy with Humate-P concentrate. The coagulation abnormalities improved partially after splenectomy and completely after subsequent chemotherapy. The neoplastic lymphocytes in the blood and spleen strongly expressed platelet glycoprotein Ib (CD42) and VWF but not other platelet-associated antigens.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Antigens, Human Platelet / analysis
  • Female
  • Flow Cytometry
  • Humans
  • Immunophenotyping
  • Leukemia, Lymphocytic, Chronic, B-Cell / metabolism
  • Lymphoma, B-Cell / blood
  • Lymphoma, B-Cell / complications*
  • Lymphoma, B-Cell / surgery
  • Platelet Glycoprotein GPIb-IX Complex / metabolism*
  • Splenectomy
  • Splenic Neoplasms / blood
  • Splenic Neoplasms / complications*
  • Splenic Neoplasms / surgery
  • von Willebrand Diseases / blood
  • von Willebrand Diseases / etiology*

Substances

  • Antigens, Human Platelet
  • Platelet Glycoprotein GPIb-IX Complex