Renal oncocytoma with t(5;12;11), der(1)1;8) and add(19): "true" oncocytoma or chromophobe adenoma?

Int J Cancer. 1997 Nov 14;73(4):521-4. doi: 10.1002/(sici)1097-0215(19971114)73:4<521::aid-ijc11>3.0.co;2-c.

Abstract

Renal oncocytomas reveal a considerable (cyto)genetic heterogeneity. At least 2 genetic subsets are currently recognized, characterized by (1) translocations involving breakpoint 11q13 and (2) the combined loss of chromosomes 1 and X/Y. We present a case of oncocytoma revealing a 3-way translocation involving breakpoint 11q13, a der(1)t(1;8) and an add(19). The der(1) resulted in loss of chromosome 1 sequences. Using fluorescence in situ hybridization, the 11q13 breakpoint of the present case proved to be slightly different from the one observed previously in 3 cases of renal oncocytoma. Whether the 11q13 breakpoint observed in our case resides in or near another gene remains to be elucidated.

Publication types

  • Case Reports

MeSH terms

  • Adenoma, Oxyphilic / genetics*
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 1 / genetics*
  • Chromosomes, Human, Pair 11 / genetics*
  • Chromosomes, Human, Pair 12 / genetics*
  • Chromosomes, Human, Pair 19 / genetics*
  • Chromosomes, Human, Pair 5 / genetics*
  • Chromosomes, Human, Pair 8 / genetics*
  • Humans
  • Kidney Neoplasms / genetics*
  • Male
  • Middle Aged
  • Translocation, Genetic / genetics*