Acquisition of loss of the wild-type NRAS locus with aggressive disease progression in a patient with juvenile myelomonocytic leukemia and a heterozygous NRAS mutation

Haematologica. 2007 Nov;92(11):1576-8. doi: 10.3324/haematol.11503.

Abstract

In a patient with juvenile myelomonocytic leukemia, a NRAS mutation at codon 12 (GGT>TGT) was initially heterozygous, but became homozygous after blastic crisis (BC). According to microsatellite and FISH analyses, the post-BC homozygous mutation might result from the loss of the wild-type NRAS locus through mitotic recombination.

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Disease Progression
  • Genes, ras / genetics*
  • Heterozygote
  • Humans
  • Infant
  • Leukemia, Myelomonocytic, Juvenile / genetics*
  • Leukemia, Myelomonocytic, Juvenile / pathology
  • Male
  • Mutation*