Evans syndrome is a rare disorder characterized by combined autoimmune thro
mbocytopenia (ITP) and autoimmune hemolytic anemia (AIHA). Standard treatme
nts consist of transfusions, corticosteroids, splenectomy, IVIG, anabolic s
teroids, vincristine, alkylating agents, or cyclosporine. In a patient with
refractory disease, an allogeneic hematopoietic stem cell transplant (HSCT
) resulted in complete clinical and serologic remission for more than 30 mo
nths. Allogeneic HSCT may be the only current curative therapy for Evans sy
ndrome but may also be complicated by significant toxicities.