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Complete response to tacrolimus in a child with severe aplastic anemia resistant to cyclosporin A.

Abstract
Aplastic anemia (AA) is a rare disorder in children, usually treated with immunosuppressive therapy (IST) including antithymocyte globulin (ATG) and cyclosporin A. There are no current widely used alternative therapies with comparable efficacy. We describe a child with severe aplastic anemia (SAA), who developed severe gingival hyperplasia secondary to cyclosporin A, unresponsive to intensive dental intervention. When IST was changed to tacrolimus there was a significant improvement in the gingival hyperplasia, but equally important, he achieved complete response of his AA within several months. The use of tacrolimus in children with AA may be a potential modality of treatment.
AuthorsChristine Macartney, Marshall Freilich, Isaac Odame, Karen Charpentier, Yigal Dror
JournalPediatric blood & cancer (Pediatr Blood Cancer) Vol. 52 Issue 4 Pg. 525-7 (Apr 2009) ISSN: 1545-5017 [Electronic] United States
PMID19058202 (Publication Type: Case Reports, Journal Article)
CopyrightCopyright 2008 Wiley-Liss, Inc.
Chemical References
  • Immunosuppressive Agents
  • Cyclosporine
  • Tacrolimus
Topics
  • Anemia, Aplastic (drug therapy, physiopathology)
  • Anemia, Refractory (drug therapy, physiopathology)
  • Child
  • Cyclosporine (adverse effects)
  • Gingival Hyperplasia (chemically induced)
  • Humans
  • Immunosuppressive Agents (therapeutic use)
  • Male
  • Tacrolimus (therapeutic use)

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