| Literature DB >> 27107757 |
Kyogo Suzuki1, Hideki Muramatsu1, Yusuke Okuno1, Atsushi Narita1, Asahito Hama1, Yoshiyuki Takahashi1, Makoto Yoshida2, Yasuo Horikoshi3, Ken-Ichiro Watanabe3, Kazuko Kudo4, Seiji Kojima5.
Abstract
Idiopathic aplastic anemia (AA) is a rare hematological complication of Down syndrome (DS). The safety and efficacy of immunosuppressive therapy (IST) in individuals with DS remain unknown. We used a standard regimen of IST, comprising antithymocyte globulin and cyclosporine A, to treat three children with DS and idiopathic acquired AA. Two patients achieved a hematological (complete or partial) response and became transfusion independent at the final follow-up. The third patient failed to respond to IST and underwent bone marrow transplantation from a human leukocyte antigen (HLA)-mismatched unrelated donor. None of the patients experienced severe or unexpected adverse events during IST. Our experience suggests that IST is a safe and reasonable treatment, even in individuals with DS who suffer from AA and lack an HLA-matched sibling donor.Entities:
Keywords: Aplastic anemia; Down syndrome; Immunosuppressive therapy
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Year: 2016 PMID: 27107757 DOI: 10.1007/s12185-016-1997-z
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490