Cytogenetic patterns in acute nonlymphocytic leukemia

Joseph R. Testa, Janet D. Rowley

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

Analysis of chromosomal banding patterns in acute nonlymphocytic leukemia (ANLL) reveals that approximately 50% of patients have an abnormal karyotype. Although there is substantial variability, certain nonrandom abnormalities occur, e.g., +8, -7, and the 8;21 translocation (often accompanied by loss of an X or Y chromosome). The 15;17 translocation appears to be highly specific for acute promyelocytic leukemia. These abnormalities usually are not seen in remission, but reappear in relapse, sometimes exhibiting further clonal evolution; a +8 is the most frequently observed evolutionary change. Patients with ANLL following treatment of a malignant lymphoma tend to have hypodiploid modal numbers and frequently show loss of a chromosome No. 5 or No. 7.

Original languageEnglish
Pages (from-to)65-72
Number of pages8
JournalVirchows Archiv B Cell Pathology
Volume29
Issue number1-2
DOIs
StatePublished - Dec 1978

Keywords

  • Acute Disease
  • Bone Marrow/pathology
  • Chromosome Aberrations/complications
  • Chromosome Banding
  • Chromosome Disorders
  • Chromosomes, Human, 13-15
  • Chromosomes, Human, 16-18
  • Chromosomes, Human, 21-22 and Y
  • Chromosomes, Human, 6-12 and X
  • Humans
  • Leukemia/complications
  • Remission, Spontaneous
  • Translocation, Genetic

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