Myelodysplastic syndrome with hypereosinophilia and a nonrandom chromosomal abnormality dic(1;7): confirmation of eosinophil clonal involvement by fluorescence in situ hybridization

Cancer Genet Cytogenet. 1998 Nov;107(1):65-8. doi: 10.1016/s0165-4608(98)00055-7.

Abstract

We report a case of de novo myelodysplastic syndrome (MDS) with hypereosinophilia and dic(1;7) in which eosinophil clonal involvement was confirmed by fluorescence in situ hybridization. There have been two previous reports in the literature of eosinophilic MDS with dic(1;7) or t(1;7) in which eosinophil clonality was demonstrated. The specific breakpoints on chromosomes 1 and 7 differ in the three cases, making it difficult to implicate disruption of a single gene as causative; nevertheless, the nonrandom occurrence of t(1;7) or dic(1;7) with malignant eosinophilic proliferations suggests that this chromosomal rearrangement is involved in the etiology of the disease.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Anemia, Refractory / complications
  • Anemia, Refractory / genetics*
  • Chromosomes, Human, Pair 1 / genetics*
  • Chromosomes, Human, Pair 7 / genetics*
  • Fatal Outcome
  • Genetic Markers
  • Humans
  • Hypereosinophilic Syndrome / complications
  • Hypereosinophilic Syndrome / genetics*
  • Male
  • Translocation, Genetic*

Substances

  • Genetic Markers