Leukemia Research Reports (Jan 2022)

Rare evolution of CSF3R-mutated chronic neutrophilic leukemia to t(4;12)(q12;p13) acute myeloid leukemia with SETBP1 mutation

  • Maki Hirao,
  • Kentaro Watanabe,
  • Yuiko Tsukada,
  • Hisako Kunieda,
  • Makoto Osada,
  • Kohei Yamazaki,
  • Ryunosuke Denda,
  • Shinichiro Okamoto,
  • Takahide Kikuchi

Journal volume & issue
Vol. 17
p. 100311

Abstract

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Chronic neutrophilic leukemia (CNL) is a rare myeloproliferative disease accompanied by mutations in CSF3R. Here, we present a patient with CNL who developed to acute myeloid leukemia (AML) at the same time that a t(4;12)(q12;p13) translocation appeared. The uniqueness of this cytogenetic abnormality led us to delineate the molecular aberrations relevant for clonal evolution. While the CSF3R mutation was present throughout the course of the disease, the SETBP1 mutation was newly acquired at the AML transformation. The present case suggests that careful monitoring of t(4;12)(q12;p13) and SETBP1 is crucial to predict AML evolution in CNL patients.

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