Hematology Reports (Jun 2024)

Three-Way Translocation t(12;15;17) (p13;q24;q21) Found in Acute Promyelocytic Leukemia with Basophilic Differentiation

  • Sara Frazzetto,
  • Lara Gullo,
  • Gabriele Sapuppo,
  • Manlio Fazio,
  • Cristina Lo Faro,
  • Giuliana Giunta,
  • Ignazio Caravotta,
  • Elisa Mauro,
  • Marina Silvia Parisi,
  • Anna Maria Triolo,
  • Nunziatina Laura Parrinello,
  • Maria Letizia Consoli,
  • Loredana També,
  • Daniela Cambria,
  • Sara Marino,
  • Grazia Scuderi,
  • Francesco Di Raimondo

DOI
https://doi.org/10.3390/hematolrep16020037
Journal volume & issue
Vol. 16, no. 2
pp. 367 – 374

Abstract

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Acute promyelocytic leukemia is a rare form of acute myeloid leukemia in which immature promyelocytes abnormally proliferate in the bone marrow. In most cases, the disease is characterised by the translocation t(15;17) (q24;q21), which causes the formation of PML::RARA, an oncogenic fusion protein responsible for blocking myeloid differentiation and survival advantage. Here, we present a case of acute promyelocytic leukemia with two unusual features: basophilic differentiation and a three-way translocation involving chromosomes 12, 15 and 17. In the few cases reported, basophilic differentiation was associated with a poor prognosis. In contrast, our patient responded promptly to the standard treatment with all-trans-retinoic acid (ATRA) and arsenic trioxide (ATO) and obtained complete remission. To our knowledge, this is the first report of basophilic acute promyelocytic leukemia with the three-way translocation t(12;17;15) (p13; q24;q21).

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