t(1;19)(q23;p13) in a case of acute monocytic leukemia

Cancer Genet Cytogenet. 1996 Mar;87(1):52-4. doi: 10.1016/0165-4608(95)00238-3.

Abstract

Translocation (1;19)(q23;p13) is considered a specific chromosome aberration in acute lymphoblastic leukemia (ALL). We report a case of M5 acute nonlymphocytic leukemia (ANLL) with t(1;19). In all mitoses studied from peripheral blood (PB) cells, the pathological karyotype 51,XX,t(1;19)(q23;p13),+8, +der(19)t(1;19)(q23;p13), +3mar was detected. No rearrangement of the E2A gene was detected. We believe this case shows that cytogenetically indistinguishable aberrations may be accompanied by quite different molecular events.

Publication types

  • Case Reports

MeSH terms

  • Chromosomes, Human, Pair 1*
  • Chromosomes, Human, Pair 19*
  • Humans
  • In Situ Hybridization, Fluorescence
  • Leukemia, Monocytic, Acute / genetics*
  • Middle Aged
  • Translocation, Genetic*