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      Severe autoimmune hemolytic anemia complicating hereditary spherocytosis treated successfully with glucocorticoids and cyclosporine: a case report.

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          Abstract

          Severe autoimmune hemolytic anemia complicating hereditary spherocytosis is life threatening and has not been described in a case report. Here, we report a case in which this intractable disease was treated successfully with glucocorticoids and cyclosporine.

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          Author and article information

          Journal
          Journal ID (iso-abbrev): Hematology
          Title: Hematology (Amsterdam, Netherlands)
          Publisher: Informa UK Limited
          ISSN (Electronic): 1607-8454
          ISSN (Print): 1024-5332
          Publication date (Electronic): Dec 2023
          Volume: 28
          Issue: 1
          Affiliations
          [1 ] Department of Blood Transfusion, China-Japan Friendship Hospital, Beijing, People's Republic of China.
          [2 ] Clinical Laboratory, China-Japan Friendship Hospital, Beijing, People's Republic of China.
          [3 ] Department of Hematology, China-Japan Friendship Hospital, Beijing, People's Republic of China.
          Article
          DOI: 10.1080/16078454.2023.2235832
          PubMed ID: 37504499
          SO-VID: 8cd00e7e-9e5a-4bd2-aeb1-44de04800733
          History

          Keywords: hereditary spherocytosis,β-spectrin,‌congenital anemia,‌glucocorticoids,Autoimmune hemolytic anemia,anti-red blood cell antibodies,alloantibodies,cyclosporine
          Data availability:
          Keywords: hereditary spherocytosis, β-spectrin, ‌congenital anemia, ‌glucocorticoids, Autoimmune hemolytic anemia, anti-red blood cell antibodies, alloantibodies, cyclosporine

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