Acute promyelocytic leukemia: cytogenetics and bone-marrow culture

Int J Cancer. 1981 Feb 15;27(2):167-73. doi: 10.1002/ijc.2910270207.

Abstract

Six patients were diagnosed as having acute promyelocytic leukemia (APL) according to FAB criteria. One patient conformed to the M3 variant. Informative cytogenetic results (G-banding) on five of the patients showed that three of them, including the M3 variant, had the 15;17 translocation in bone-marrow or blood cells. Cells with the translocation were accompanied by cells with a normal karyotype in all patients and no other chromosomal abnormality was present. This first report of the 15;17 translocation from the South Pacific region is relevant to the uneven geographical distribution of APL patients with the translocation. Five of the six patients including the M3 variant, showed a distinctive pattern of cell growth in agar culture characterized by a profusion of small, uniform clusters containing 6-20 cells with the appearance of promyelocytes. The remaining patient had a pattern of cell growth more typical of M2 acute leukemia. This cell growth pattern may be useful in diagnosing and monitoring the course of APL.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Blood Cells / ultrastructure
  • Bone Marrow / ultrastructure
  • Child
  • Chromosome Banding
  • Chromosomes, Human, 13-15
  • Chromosomes, Human, 16-18
  • Culture Media
  • Female
  • Humans
  • Leukemia, Myeloid, Acute / genetics*
  • Male
  • Microscopy, Electron
  • Middle Aged
  • New Zealand
  • Translocation, Genetic

Substances

  • Culture Media