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  • Response of pure red cell a...
    Orlova, Elizaveta M; Kareva, Maria A; Melikyan, Maria A; Boyakova, Elena; Peterkova, Valentina A; Maschan, Alexey A

    Journal of pediatric hematology/oncology, 11/2013, Letnik: 35, Številka: 8
    Journal Article

    A 26-year-old female with the classic major and minor components of autoimmune polyglandular syndrome type 1 was diagnosed as having pure red cell aplasia. Treatment with 1.5 g/d mycofenolate mofetil for 3 months failed to restore erythroid production. Treatment with cyclosporine A produced a good partial response but led to renal toxicity and was therefore substituted with cyclophosphamide, which had a good partial effect and lasted for 18 months. The relapse of anemia was not observed during the 6-month follow-up period after the cessation of treatment.