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Chronic thrombocytopenia in an immunodeficient patient with hemophilia A
Authors:Viola Hach  L Bergmann  I Scharrer  P Mitrou  C Mueller-Eckhardt
Institution:(1) Abteilung Innere Medizin, Klinikum der Johann Wolfgang Goethe Universität, Theodor-Stern-Kai 7, D-6000 Frankfurt 70, Federal Republic of Germany;(2) Institut für Klinische Immunologie und Transfusionsmedizin, Justus Liebig Universität, D-6300 Gießen, Federal Republic of Germany
Abstract:Summary Coincident hemophilia and idiopathic thrombocytopenia has been rarely observed. We report here on a young man with severe hemophilia A who was treated with concentrates of lyophilized antihemophilic factor for several years before he developed thrombocytopenia. An isolated thrombocytopenia coincident with reduced platelet survival, ample megacaryocytes in the bone marrow, elevated platelet-associated IgG, as well as remission after treatment with prednisone and splenectomy, suggest the idiopathic form of thrombocytopenia. In addition, defects in cellular immunity became obvious. A causal relationship between the application of blood-derived products and the development of the platelet disorder as well as the impairment of the T-cell system remain to be demonstrated.
Keywords:Hemophilia  Idiopathic thrombocytopenia  High-dose immunoglobulin therapy  Splenectomy  T-cell defect
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