Ticlopidine-Associated thrombotic thrombocytopenic purpura with an IgG-type inhibitor to von Willebrand factor-cleaving protease activity

Int J Hematol. 2001 Oct;74(3):347-51. doi: 10.1007/BF02982073.

Abstract

A 41-year-old Japanese man complained of a left-sided visual disturbance. Imaging by magnetic resonance angiography revealed a narrowing of the left internal cervical artery. Thus, ticlopidine (Tc) administration was started at a daily dose of 300 mg. However, 2 weeks later, severe thrombocytopenia, fever, nausea, and psychiatric symptoms developed; Tc was therefore discontinued. Based on the diagnostic hallmark of 5 clinical signs, the patient's disease was diagnosed as thrombotic thrombocytopenic purpura (TTP). Daily plasmapheresis was performed for the first 4 days, and the patient's clinical signs gradually improved. Von Willebrand factor-cleaving protease (vWF-CPase) activity in his plasma was less than 3% of that of the control sample at diagnosis, but that value recovered steadily following plasmapheresis. In addition, immunoglobulin G purified from the patient plasma inhibited vWF-CPase activity in normal plasma with a specific activity of 0.8 Bethesda units/mg. No sign of TTP relapse has been noted following cessation of Tc. Thus, it was concluded that the patient developed TTP by producing an inhibitory autoantibody against vWF-CPase activity that was presumably triggered by Tc administration.

Publication types

  • Case Reports

MeSH terms

  • ADAM Proteins
  • ADAMTS13 Protein
  • Adult
  • Arterial Occlusive Diseases / diagnosis
  • Arterial Occlusive Diseases / drug therapy
  • Autoantibodies / immunology*
  • Humans
  • Immunoglobulin G / immunology*
  • Male
  • Metalloendopeptidases / blood*
  • Platelet Aggregation Inhibitors / administration & dosage
  • Platelet Aggregation Inhibitors / adverse effects*
  • Purpura, Thrombotic Thrombocytopenic / chemically induced*
  • Purpura, Thrombotic Thrombocytopenic / immunology
  • Ticlopidine / administration & dosage
  • Ticlopidine / adverse effects*

Substances

  • Autoantibodies
  • Immunoglobulin G
  • Platelet Aggregation Inhibitors
  • ADAM Proteins
  • Metalloendopeptidases
  • ADAMTS13 Protein
  • ADAMTS13 protein, human
  • Ticlopidine