Coincident classic hemophilia and "idiopathic" thrombocytopenic purpura in patients under treatment with concentrates of antihemophilic factor (factor VIII)

N Engl J Med. 1983 Feb 24;308(8):439-42. doi: 10.1056/NEJM198302243080808.
No abstract available

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Factor VIII / administration & dosage
  • Factor VIII / adverse effects*
  • Freeze Drying
  • Hemophilia A / complications*
  • Hemophilia A / diagnosis
  • Hemophilia A / immunology
  • Humans
  • Immunity, Cellular
  • Lymphocytes / immunology
  • Male
  • Purpura, Thrombocytopenic / complications*
  • Purpura, Thrombocytopenic / diagnosis
  • Purpura, Thrombocytopenic / etiology
  • Purpura, Thrombocytopenic / immunology
  • Purpura, Thrombocytopenic / therapy

Substances

  • Factor VIII