Essential thrombocythemia in a child with elevated thrombopoietin concentrations and skeletal anomalies.

TitleEssential thrombocythemia in a child with elevated thrombopoietin concentrations and skeletal anomalies.
Publication TypeJournal Article
Year of Publication2008
AuthorsRobins EB, Niazi M
JournalPediatr Blood Cancer
Volume50
Issue4
Pagination859-61
Date Published2008 Apr
ISSN1545-5017
KeywordsAspirin, Bone and Bones, Child, Preschool, Enzyme Inhibitors, Female, Humans, Hydroxyurea, Male, Mothers, Pedigree, Platelet Count, Thrombocythemia, Essential, Thrombopoietin
Abstract

Essential thrombocythemia is a rare myleoproliferative disorder in pediatrics. This myeloproliferative disorder is characterized by excessive proliferation of megakaryocytes and sustained elevation of platelet count. Reactive thrombocytosis is a more common cause of elevated platelet counts among children. We describe a 2-year-old child with essential thrombocythemia, skeletal anomalies, and elevated thrombopoietin concentrations. The child's mother was also subsequently diagnosed with essential thrombocythemia and had elevated thrombopoietin concentrations. Chromosomal studies on the mother, child and other family members were normal.

DOI10.1002/pbc.21218
Alternate JournalPediatr Blood Cancer
PubMed ID17455310

Richard T. Silver MD Myeloproliferative Neoplasms Center 525 East 70th St., Starr Pavillion, 3rd Floor New York, NY 10021 SilverMPNCenter@med.cornell.edu