Trisomy 13: a preferentially male chromosome aberration interfering specifically with myeloid proliferation and differentiation? Report of a case and review of the literature

Cancer Genet Cytogenet. 1991 Nov;57(1):79-85. doi: 10.1016/0165-4608(91)90192-w.

Abstract

A case of trisomy 13 is presented: a 73-year-old man with acute nonlymphocytic leukemia (ANLL), FAB borderline M1/M2, and peripheral leukocyte and platelet counts that were difficult to control with chemotherapy. A literature review shows that 35 cases of trisomy 13 are known at present. They are characterized by male predominance (76%), preferentially myeloid disorders (ANLL, myelodysplastic syndromes, chronic myeloid leukemia), leucocytosis, and relatively high platelet counts and hemoglobins. It is suggested that trisomy 13 is a specific nosologic entity with male predominance and characterized by interference with proliferation and differentiation in the myeloid differentiation series.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Chromosome Aberrations / pathology*
  • Chromosome Banding
  • Chromosome Disorders
  • Chromosomes, Human, Pair 13*
  • Humans
  • Leukemia / pathology
  • Leukemia, Myeloid, Acute / pathology*
  • Male
  • Sex Factors
  • Survival Analysis
  • Trisomy*