Acute myeloid leukemia with translocation (1;21)

Mol Biol Rep. 2018 Jun;45(3):347-351. doi: 10.1007/s11033-018-4168-x. Epub 2018 Mar 22.

Abstract

Advancement in genetic and molecular biology techniques has greatly helped our understanding of various diseases, especially hematological disorders. We describe a case of primary myelofibrosis (PMF) that transformed into acute myeloid leukemia with a very rare and unusual genetic translocation of (1;21). There are only five reported cases of this translocation in acute myeloid leukemia (AML) or myelodysplastic syndrome but none of them transformed from PMF. This case not only highlights the importance of rare genetic translocations but also provides the natural history of the disease and its poor prognosis. To the best of our knowledge our patient is the first reported case of AML transformed from PMF to have this unique translocation of (1;21).

Keywords: AML transformation; Acute myeloid leukemia; Primary myelofibrosis; Translocation (1;21).

Publication types

  • Case Reports
  • Review

MeSH terms

  • Chromosomes, Human, Pair 1 / genetics*
  • Chromosomes, Human, Pair 21 / genetics*
  • Female
  • Humans
  • Leukemia, Myeloid, Acute / genetics*
  • Middle Aged
  • Myelodysplastic Syndromes / genetics
  • Primary Myelofibrosis / genetics
  • Prognosis
  • Translocation, Genetic / genetics