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Clin Ter ; 138(5-6): 213-7, 1991.
Artículo en Italiano | MEDLINE | ID: mdl-1836169

RESUMEN

Approximately 5-20% of patients with hemophilia A acquire antifactor VIII antibodies during transfusion therapy. These autoantibodies cause serious bleeding and are rarely found in non hemophiliac patients (only a few hundred case reports in the literature). Treatment of this autoimmune condition is quite difficult: corticosteroids, immunosuppressive agents, plasmapheresis and transfusions may be useful. We describe two patients we observed and add some general reflections on therapy.


Asunto(s)
Autoanticuerpos/análisis , Enfermedades Autoinmunes , Factor VIII/inmunología , Corticoesteroides/uso terapéutico , Adulto , Enfermedades Autoinmunes/terapia , Transfusión Sanguínea , Femenino , Humanos , Inmunosupresores/uso terapéutico , Plasmaféresis , Pronóstico
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