Translocation (10;11)(p13;q13) and MLL gene rearrangement in a case of AML (M5a) with aggressive leukemia cutis

Cancer Genet Cytogenet. 1998 Jul 1;104(1):28-31. doi: 10.1016/s0165-4608(97)00414-7.

Abstract

A male patient with a secondary acute monocytic leukemia whose leukemia cells had a t(10;11)(p13;q13) chromosomal abnormality is described. Gene analysis disclosed that the patient's leukemia cells had MLL gene rearrangement. His leukemia cells responded poorly to chemotherapy, and the patient developed an unusual aggressive leukemia cutis. A t(10;11)(p13;q13) chromosomal abnormality that expresses MLL gene rearrangement has not been reported previously in secondary leukemia.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Chromosomes, Human, Pair 10 / genetics*
  • Chromosomes, Human, Pair 11 / genetics*
  • DNA-Binding Proteins / genetics*
  • Histone-Lysine N-Methyltransferase
  • Humans
  • Karyotyping
  • Leukemia, Monocytic, Acute / genetics*
  • Leukemia, Monocytic, Acute / pathology
  • Leukemic Infiltration*
  • Male
  • Myeloid-Lymphoid Leukemia Protein
  • Neoplasms, Second Primary / genetics
  • Neoplasms, Second Primary / pathology
  • Prostatic Neoplasms / genetics
  • Prostatic Neoplasms / pathology
  • Proto-Oncogenes*
  • Skin / pathology*
  • Transcription Factors*
  • Translocation, Genetic / genetics*

Substances

  • DNA-Binding Proteins
  • KMT2A protein, human
  • Transcription Factors
  • Myeloid-Lymphoid Leukemia Protein
  • Histone-Lysine N-Methyltransferase