Abstract
Treatment of autoimmune hemolytic anemia with corticosteroids, splenectomy, immune suppression, and plasma exchange, serially or in combination, often yields partial or short remissions. We describe a patient in whom refractory autoimmune hemolytic anemia was moderated by selective impairment of the mononuclear-phagocyte system by means of infusion of vinblastine-loaded platelets. The success of this approach, initially proposed for treatment of immune thrombocytopenic purpura, suggests that erythrocytes and platelets share a common site of immune destruction and that the rate of this destruction is determined by the phagocyte.
Original language | English (US) |
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Pages (from-to) | 325-326 |
Number of pages | 2 |
Journal | Unknown Journal |
Volume | 95 |
Issue number | 3 |
DOIs | |
State | Published - Jan 1 1981 |
ASJC Scopus subject areas
- Internal Medicine