A patient with a 20-year lag phase between JAK2-V617F+ myeloproliferation and NPM1-mutated AML arguing against a common origin of disease

Eur J Haematol. 2011 Nov;87(5):461-3. doi: 10.1111/j.1600-0609.2011.01669.x. Epub 2011 Aug 11.

Abstract

We have sought to unravel the molecular biology of a female patient who in 1985 at the age of 55 was diagnosed with a chronic myeloproliferative neoplasm (MPN) and in whom overt acute myeloid leukemia (AML) developed in 2005. To this end, DNA and RNA (extracted from either paraffin-embedded bone marrow (BM) or from BM and/or peripheral blood stored in an RNA/DNA-preserving buffer) were analyzed by qPCR and by capillary gel electrophoresis of PCR products. We found the patient to be JAK2-V617F mutation positive throughout the course of disease, while a mutation of the nucleophosmin (NPM1) gene emerged at AML diagnosis and relapse. The 20-yr lag phase between the polycythemia vera and the AML adds indirect evidence to the growing realization that the leukemic transformation in patients with MPN occurs from in a JAK2 wild-type stem cell.

Publication types

  • Case Reports

MeSH terms

  • Electrophoresis, Capillary
  • Female
  • Humans
  • Janus Kinase 2 / genetics*
  • Leukemia, Myeloid, Acute / genetics*
  • Middle Aged
  • Myeloproliferative Disorders / genetics*
  • Nuclear Proteins / genetics*
  • Nucleophosmin
  • Polymerase Chain Reaction

Substances

  • NPM1 protein, human
  • Nuclear Proteins
  • Nucleophosmin
  • Janus Kinase 2