Simultaneous occurrence of myelodysplastic syndrome and monoclonal B lymphocytes with a different clonal origin

Leuk Lymphoma. 2002 Jan;43(1):191-3. doi: 10.1080/10428190210205.

Abstract

Bone marrow and peripheral blood from a myelodysplastic syndrome patient with trisomy 13 and monoclonal B lymphocytes (without evidence of systemic lymphoma) were investigated for clonal lymphoid lineage involvement using interphase fluorescence in situ hybridization (FISH) and X-chromosome inactivation assay (HUMARA) on CD19+ and CD34+ sorted cells. Trisomy 13 was detected in 55% of CD34+ cells and in 5.5% of CD19+ cells, the latter being comparable to the negative control specimen. X-chromosome inactivation showed both CD34+ and CD19+ cells to be monoclonal, though their inactivated X-chromosome was different. The results strongly suggested that both populations of CD34+ and CD19+ cells have originated from a different progenitor stem cell.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • B-Lymphocytes / pathology*
  • Cell Lineage
  • Cell Transformation, Neoplastic / pathology*
  • Chromosomes, Human, Pair 13
  • Clone Cells / pathology
  • Cytogenetic Analysis
  • Female
  • Flow Cytometry
  • Humans
  • Myelodysplastic Syndromes / pathology*
  • Trisomy