Cytogenetics of a renal cell carcinoma in a 17-month-old child. Evidence for Xp11.2 as a recurring breakpoint

Cancer Genet Cytogenet. 1991 Nov;57(1):11-7. doi: 10.1016/0165-4608(91)90184-v.

Abstract

A renal cell carcinoma from a 17-month-old boy with a history of maternal hydrocarbon exposure was found to have a 46,Y,t(X;17)(p11.2;q25) karyotype. Although this translocation has not previously been reported, other translocations involving Xp11.2 have been described, suggesting that this may represent a non-random breakpoint involved in the pathogenesis of childhood renal cell carcinoma. Both chromosomes 3 in the tumor were normal by both karyotype and RFLP analysis.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Carcinoma, Renal Cell / genetics*
  • Carcinoma, Renal Cell / pathology
  • Chromosome Aberrations / pathology*
  • Chromosome Disorders
  • Humans
  • Infant
  • Kidney Neoplasms / genetics
  • Kidney Neoplasms / pathology*
  • Male
  • Polymorphism, Restriction Fragment Length
  • Translocation, Genetic
  • X Chromosome