Reemergence of translocation t(11;19)(q23;p13.1) in the absence of clinically overt leukemia

Int J Hematol. 2017 Dec;106(6):847-851. doi: 10.1007/s12185-017-2289-y. Epub 2017 Jul 1.

Abstract

We report the case of a 10-year-old female with acute myeloid leukemia (AML) FAB M0 carrying a novel t(11;19)(q23;p13.1) MLL-ELL variant, in which intron 8 of MLL is fused to exon 6 of ELL. Complete remission, judged by morphology and cytogenetic analysis, was achieved after the conventional chemotherapy. Eight months after completion of therapy, the level of WT-1 in peripheral blood and the number of cells with the MLL-ELL fusion transcript resurged. However, the patient remained overtly healthy and the morphology in the bone-marrow smear was innocuous, with no sign of relapse or secondary leukemia. Without any evidence of relapse, the patient has been closely observed without any therapeutic intervention. For approximately 2 years after the completion of therapy, despite clonal proliferation of pre-leukemic cells with an MLL-ELL fusion gene, she has maintained complete remission. In this case, the rare variant form of MLL-ELL fusion that has been identified may be related to diminished leukemogenic capacity, resulting in the persistence of pre-leukemic status; an additional genetic abnormality may thus be necessary for full transformation of pre-leukemic cells.

Keywords: AML; MLL–ELL; Pediatrics.

Publication types

  • Case Reports

MeSH terms

  • Child
  • Chromosomes, Human, Pair 11 / genetics*
  • Chromosomes, Human, Pair 19 / genetics*
  • Female
  • Humans
  • Leukemia, Myeloid, Acute / genetics
  • Leukemia, Myeloid, Acute / therapy
  • Myeloid-Lymphoid Leukemia Protein / blood
  • Myeloid-Lymphoid Leukemia Protein / genetics*
  • Oncogene Proteins, Fusion / blood
  • Oncogene Proteins, Fusion / genetics*
  • Translocation, Genetic*

Substances

  • MLL-ELL fusion protein, human
  • Oncogene Proteins, Fusion
  • Myeloid-Lymphoid Leukemia Protein