Durable response to etoposide-loaded platelets in refractory immune thrombocytopenic purpura: a case report

A 23-year-old female presented with widespread purpura and ecchymoses as a result of immune thrombocytopenia which was refractory to corticosteroids, splenectomy, and immunosuppressive agents. In view of the extent and serious nature of her bleeding, salvage therapy with etoposide-loaded platelets was undertaken, which was associated with a lasting complete remission.