Acute myeloid leukemia with translocation (1;21). Review uri icon

Overview

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).

publication date

  • March 22, 2018

Research

keywords

  • Chromosomes, Human, Pair 1
  • Chromosomes, Human, Pair 21
  • Leukemia, Myeloid, Acute

Identity

Scopus Document Identifier

  • 85047542036

Digital Object Identifier (DOI)

  • 10.1007/s11033-018-4168-x

PubMed ID

  • 29569103

Additional Document Info

volume

  • 45

issue

  • 3