Wild-type JAK2 secondary acute erythroleukemia developing after JAK2-V617F-mutated primary myelofibrosis

Acta Haematol. 2009;122(1):36-8. doi: 10.1159/000235773. Epub 2009 Aug 28.

Abstract

A 54-year-old female patient developed acute erythroleukemia after an 8-year course of primary myelofibrosis. The latter harbors the JAK2-V617F mutation and was treated with hydroxyurea and anagrelide. A bone marrow trephine biopsy disclosed 2 morphologically distinct areas of chronic primary myelofibrosis and acute erythroleukemia. Microdissection and a separate molecular pathological analysis was performed. Although the activating JAK2-V617F mutation was not maintained in blasts of acute erythroleukemia, it was detectable in the chronic phase of primary myelofibrosis, indicating that this mutation did not play a role in the leukemic transformation of erythroid cells.

Publication types

  • Case Reports

MeSH terms

  • Cell Transformation, Neoplastic / genetics
  • Fatal Outcome
  • Female
  • Humans
  • Janus Kinase 2 / genetics*
  • Leukemia, Erythroblastic, Acute / etiology
  • Leukemia, Erythroblastic, Acute / genetics*
  • Middle Aged
  • Primary Myelofibrosis / complications*
  • Primary Myelofibrosis / genetics*

Substances

  • Janus Kinase 2