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Stem cell transplantation in primary myelofibrosis of childhood.

Abstract
Fewer than 40 cases of primary myelofibrosis have been reported in children; hematopoietic stem cell transplantation is the only available curative therapy for this disease. Here, we describe the case of a female infant diagnosed with primary myelofibrosis at the age of 6 months; she underwent successful matched unrelated bone marrow transplantation with complete resolution of disease. We discuss some unique characteristics of primary myelofibrosis in children and review outcome data for children with this disease.
AuthorsBryan Mitton, Satiro de Oliveira, Sheeja T Pullarkat, Theodore B Moore
JournalJournal of pediatric hematology/oncology (J Pediatr Hematol Oncol) Vol. 35 Issue 3 Pg. e120-2 (Apr 2013) ISSN: 1536-3678 [Electronic] United States
PMID23511496 (Publication Type: Case Reports, Journal Article)
Topics
  • Bone Marrow Transplantation
  • Female
  • Humans
  • Infant
  • Primary Myelofibrosis (diagnosis, therapy)
  • Treatment Outcome

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