Myelodysplastic syndrome in a child with constitutional trisomy 8 mosaicism and normal phenotype

Cancer Genet Cytogenet. 1995 Jan;79(1):79-81. doi: 10.1016/0165-4608(94)00099-w.

Abstract

Trisomy 8 is a frequently acquired cytogenetic abnormality in myeloid malignancies, but may also represent a constitutional chromosome abnormality with a wide phenotypic variation. We report a case of myelodysplastic syndrome (MDS) that developed in a child with trisomy 8 mosaicism and normal phenotype. Bone marrow (BM) cells all showed trisomy 8 with additional clonal abnormalities in most cells. Based on the present case and a review of previously published cases of myeloid malignancies in patients with trisomy 8 mosaicism, it appears likely that the malignant cells developed from the trisomic cell population, suggesting that constitutional trisomy 8 may be a predisposing condition to myeloid malignancies. Trisomy 8 in malignant cells is usually considered an acquired abnormality, but this implies a risk of ignoring a constitutional trisomy 8 mosaicism. Examination for constitutional trisomy 8, despite a normal phenotype, may therefore be warranted in hematologic malignancies with trisomy 8 of BM cells to evaluate further the possible association and to preclude erroneous use of trisomy 8 as a tumor marker.

Publication types

  • Case Reports

MeSH terms

  • Child
  • Chromosomes, Human, Pair 8*
  • Humans
  • Karyotyping
  • Male
  • Mosaicism*
  • Myelodysplastic Syndromes / genetics*
  • Phenotype
  • Trisomy / genetics*