Complex variant t(4;11) characterized by fluorescence in situ hybridization in infant acute lymphoblastic leukemia

Cancer Genet Cytogenet. 2001 Jun;127(2):177-80. doi: 10.1016/s0165-4608(00)00439-8.

Abstract

A 6-month-old girl was diagnosed with acute lymphoblastic leukemia (ALL). Chromosome analysis of bone marrow aspirate showed 46,XX,t(4;11)(q21;q23) with an atypical appearance of the 11p on the der(11) chromosome. FISH studies to fully characterize the translocation utilised 8 probes: whole chromosome painting probes for chromosome 11 and chromosome 4; separate chromosome 11 short arm and long arm paints; specific subtelomere probes from 11p, 11q, and 4q; MLL gene probe. Taken together, the results indicated a two-step abnormality: an initial standard t(4;11)(q21;q23), followed by another t(4;11)--this time, between the two derivative chromosomes. The MLL gene was split by the first translocation and its position altered by the second.

Publication types

  • Case Reports

MeSH terms

  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Bone Marrow Cells / pathology
  • Chromosome Deletion
  • Chromosome Mapping
  • Chromosome Painting
  • Chromosomes, Human, Pair 11*
  • Chromosomes, Human, Pair 4*
  • Female
  • Genetic Variation
  • Humans
  • In Situ Hybridization, Fluorescence
  • Infant
  • Karyotyping
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / drug therapy
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / genetics*
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / pathology
  • Translocation, Genetic*