Translocation (X;8)(q2?6;q21.3) in a case of systemic mastocytosis

Cancer Genet Cytogenet. 1994 Dec;78(2):236-8. doi: 10.1016/0165-4608(94)90096-5.

Abstract

Mastocytosis is a rare disease which occasionally progresses into mast cell leukemia or other myeloid neoplasms. Here we report on a patient with systemic mastocytosis who was found to have a clone with t(X;8)(q2?6;q21.3) and two copies of der(8)t(X;8). In accordance with these results, interphase cytogenetic analysis revealed that 93% of bone marrow cells contained three centromeric regions of chromosome 8. We suggest that the t(X;8) and the duplication of the translocation chromosome 8 may play a role in the progression of the diseases.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Chromosomes, Human, Pair 8*
  • Humans
  • In Situ Hybridization, Fluorescence
  • Male
  • Mastocytosis / genetics*
  • Translocation, Genetic*
  • X Chromosome*