Translocation (X;1) associated with a nonpapillary carcinoma in a young woman: a new definition for an Xp11.2 RCC subtype

Cancer Genet Cytogenet. 1999 Sep;113(2):141-4. doi: 10.1016/s0165-4608(98)00261-1.

Abstract

We report a translocation (X;1)(p11.2;q21) associated with a nontubulopapillary renal cell carcinoma in a 23-year-old woman. To our knowledge this the first report of such an association. A review of the previously published cases of renal cell carcinoma with t(X;1) and its cytogenetic variants with Xp11.2 anomalies is included. The role of this karyotype abnormality as a clinical marker is discussed. The Xp11.2 abnormality could be a primary abnormality characterizing a particular type of RCC appearing in children and young adults of both sexes and in which the histological aspect is not specific.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Adult
  • Carcinoma, Renal Cell / genetics*
  • Chromosomes, Human, Pair 1*
  • Female
  • Humans
  • Kidney Neoplasms / genetics*
  • Male
  • Translocation, Genetic*
  • X Chromosome*