Chronic eosinophilic leukemia with recurrent STAT5B N642H mutation-An entity with features of myelodysplastic syndrome/ myeloproliferative neoplasm overlap

Leuk Res. 2022 Jan:112:106753. doi: 10.1016/j.leukres.2021.106753. Epub 2021 Nov 23.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Diagnosis, Differential
  • Humans
  • Hypereosinophilic Syndrome / diagnosis
  • Hypereosinophilic Syndrome / genetics*
  • Leukemia / diagnosis
  • Leukemia / genetics*
  • Male
  • Mutation, Missense*
  • Myelodysplastic Syndromes / diagnosis
  • Myelodysplastic Syndromes / genetics*
  • Myeloproliferative Disorders / diagnosis
  • Myeloproliferative Disorders / genetics*
  • STAT5 Transcription Factor / genetics*

Substances

  • STAT5 Transcription Factor

Supplementary concepts

  • Pdgfra-Associated Chronic Eosinophilic Leukemia