Prolonged extreme thrombocytosis associated with neurofibromatosis type 1

J Pediatr. 1997 Feb;130(2):317-9. doi: 10.1016/s0022-3476(97)70363-9.

Abstract

A girl with neurofibromatosis type 1 showed in infancy extreme thrombocytosis with platelet counts exceeding 2000 x 10(9)/L. Platelet counts remained elevated the first 4 years of life. A large deletion located at chromosome 17q11 was observed. The transient thrombocythemia may relate to a regulator of megakaryocytopoiesis located in the vicinity of the NF1 gene or to the excessive risk of chronic myelomonocytic leukemia in neurofibromatosis.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Adolescent
  • Chromosome Deletion
  • Chromosomes, Human, Pair 17 / genetics
  • Chronic Disease
  • Female
  • Genes, Neurofibromatosis 1 / genetics
  • Humans
  • Neurofibromatosis 1 / complications*
  • Neurofibromatosis 1 / diagnosis
  • Neurofibromatosis 1 / genetics
  • Platelet Count
  • Thrombocytosis / diagnosis
  • Thrombocytosis / etiology*
  • Thrombocytosis / genetics