IKZF1 deletion and co-occurrence with other aberrations in a child with chronic myeloid leukemia progressing to acute lymphoblastic leukemia

Pediatr Blood Cancer. 2019 Apr;66(4):e27570. doi: 10.1002/pbc.27570. Epub 2018 Dec 4.

Abstract

Chronic myeloid leukemia (CML) is a rare disease in children. Different from that in adults, childhood CML involves transformative events occurring over a short time period. CML transformation to lymphoid blast phase (BP) is associated with copy number abnormalities, characteristic of BCR-ABL1 positive acute lymphoblastic leukemia, but not of CML in the chronic phase. Here, we present an unusual case of CML progressing to BP in a 1.6-year-old child, harboring IKZF1, PAX5, CDKN2A, and ETV6 deletions at diagnosis. It remains to be addressed whether distinct mechanisms might account for CML pathogenesis in early childhood.

Keywords: CML; IKZF1 deletions; acute lymphoblastic leukemia; child; chronic myeloid leukemia.

Publication types

  • Case Reports

MeSH terms

  • Blast Crisis / genetics*
  • Blast Crisis / pathology
  • Female
  • Gene Deletion*
  • Humans
  • Ikaros Transcription Factor / genetics*
  • Infant
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / genetics*
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / pathology
  • Neoplasm Proteins / genetics*

Substances

  • IKZF1 protein, human
  • Neoplasm Proteins
  • Ikaros Transcription Factor