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Keywords:

  • myelodysplastic syndrome;
  • t(l;16);
  • trisomy 8;
  • FISH

The der(16)t(l;16)(qll;qll) is a frequent recurrent rearrangement in solid tumours such as breast carcinomas and Ewings sarcomas. Recently, this abnormality was described also in multiple myeloma. We identified a der(16)t(l;16)(qll;qll) in three patients with myelodysplastic syndrome, either during preleukaemic phase (n = 2) or at the time of blastic transformation (n= 1). Breakpoints were ascertained by fluorescence in situ hybridization (FISH) using specific centromeric a-satellite probes and whole chromosome painting for chromosome 1 and chromosome 16. These observations, combined with isolated cases of the literature, suggest that der(16)t(l;16)(qll; qll) is a non-random abnormality associated with myelodysplastic syndromes.