Translocation (X;19) with involvement of the inactive X chromosome in oligoblastic granulocytic leukemia

Cancer Genet Cytogenet. 1988 Oct 15;35(2):237-42. doi: 10.1016/0165-4608(88)90246-4.

Abstract

A 72-year-old female with metastatic breast cancer developed oligoblastic granulocytic leukemia 6 months after initiation of chemotherapy. Cytogenetic examination of the bone marrow cells revealed a balanced t(X;19)(q12;q13.3) as the sole abnormality in 50% of the metaphases. The remaining cells showed a normal female karyotype. The der(19) chromosome displayed consistent folding in the Xq13-q23 region in all metaphases, indicating involvement of the inactive X chromosome in translocation.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Chromosomes, Human, Pair 19*
  • Dosage Compensation, Genetic
  • Female
  • Humans
  • Karyotyping
  • Leukemia, Myeloid / genetics*
  • Leukemia, Myeloid / pathology
  • Translocation, Genetic*
  • X Chromosome*