[Acute promyelocytic leukemia and 15;17 chromosome translocation]

Zhonghua Yi Xue Za Zhi. 1989 Aug;69(8):434-7, 30.
[Article in Chinese]

Abstract

Cytogenetic studies using Giemsa R-bands after a short term culture of bone marrow or peripheral blood were done in 20 cases of acute promyelocytic leukemia (APL), including three cases of microgranular variant. As a result, t (15;17) cells were found in all the cells, and the percentages of the abnormal cells were 38-100%. In 2 cases, t(15;17) was seen in 88% and 65% of the cells in cultured specimens, whereas no such translocation was seen in direct specimens. Among 6 cases treated with tretinoin, 5 achieved complete remission, and among 14 cases treated by HOAP protocol 2 achieved complete remission. Reexamination of 4 of these cases during the stage of complete remission failed to find t(15;17). These data revealed that t(15;17) may probably be present in all cases of APL, and therefore is a very useful diagnostic criterion, especially in cases of micro granular APL. But the detection rate is determined by methodology, which requires special precaution.

Publication types

  • English Abstract

MeSH terms

  • Adolescent
  • Adult
  • Chromosomes, Human, Pair 15*
  • Chromosomes, Human, Pair 17*
  • Female
  • Humans
  • Leukemia, Promyelocytic, Acute / genetics*
  • Male
  • Middle Aged
  • Translocation, Genetic*