Possible specific chromosome change in prolymphocytic leukemia

Blood. 1983 Oct;62(4):729-36.

Abstract

The chromosomes of unstimulated and stimulated blood lymphocytes from 5 cases with B-cell prolymphocytic leukemia (PLL) were examined following the use of polyclonal B-cell activators (PBA). Banding techniques revealed a common and specific chromosome abnormality to be present in each of the cases, which was due to a translocation between chromosomes 6 and 12 (t(6;12)(q15;p13]. The fact that this specific chromosome change has not been reported in other lymphoproliferative disorders may indicate that PLL is a distinct clinical entity and different from other lymphoproliferative disorders, whether it occurs de novo or complicates chronic lymphocytic leukemia (CLL).

Publication types

  • Case Reports
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Aged
  • Chromosome Aberrations*
  • Chromosomes, Human, 1-3
  • Chromosomes, Human, 16-18
  • Chromosomes, Human, 19-20
  • Chromosomes, Human, 21-22 and Y
  • Chromosomes, Human, 6-12 and X
  • Female
  • Humans
  • Karyotyping
  • Leukemia, Lymphoid / genetics*
  • Male
  • Sex Chromosomes