Literature DB >> 17455310

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

Edwin B Robins1, Massoma Niazi.   

Abstract

Essential thrombocythemia is a rare myleoproliferative disorder in pediatrics. This myleoproliferative 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. (c) 2008 Wiley-Liss, Inc.

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Year:  2008        PMID: 17455310     DOI: 10.1002/pbc.21218

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  2 in total

1.  Asymtomatic essential thrombocythemia in a child: a rare case report.

Authors:  Majid Vafaie; Kaveh Jaseb; Majid Ghanavat; Mohamad Pedram; Tooran Rahiminia
Journal:  Int J Hematol Oncol Stem Cell Res       Date:  2013

2.  Characteristics and outcomes of patients with essential thrombocythemia or polycythemia vera diagnosed before 20 years of age: a systematic review.

Authors:  Jean-Christophe Ianotto; Natalia Curto-Garcia; Marie Lauermanova; Deepti Radia; Jean-Jacques Kiladjian; Claire N Harrison
Journal:  Haematologica       Date:  2019-01-24       Impact factor: 9.941

  2 in total

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