Two additional cases of isochromosome 21q or translocation 21q21q in hematological malignancies

Acta Haematol. 1991;86(2):111-4. doi: 10.1159/000204815.

Abstract

We report on 2 patients with isochromosome 21q [i(21q)] or translocation 21q21q [t(21q21q)] in myeloid disorders. Of 18 available cases of i(21q) or t(21q21q), 15 were found in myeloid malignancies, often secondary to a previous carcinogen exposure. Complex karyotypes were found in most cases. Four cases presented with i(21q) or t(21q21q) as the sole anomaly, and this might represent a specific entity.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Aged
  • Chromosome Aberrations*
  • Chromosomes, Human, Pair 21*
  • Humans
  • Karyotyping
  • Leukemia, Myeloid, Acute / genetics*
  • Middle Aged
  • Myeloproliferative Disorders / genetics*
  • Translocation, Genetic