The use of molecular genetic analysis in the diagnosis of renal cell carcinoma

World J Urol. 1994;12(2):69-73. doi: 10.1007/BF00184239.

Abstract

The most common genetic aberration seen in nonpapillary renal cell carcinoma is believed to be the loss or inactivation of allelic material on the short arm of chromosome 3 (3p). Two patients underwent nephrectomy at our institution, each initially receiving a histologic diagnosis of renal cell carcinoma. Molecular analysis of these tissues revealed no genetic deletion on 3p, prompting further histologic and immunohistochemical evaluation of the original specimens. These additional studies confirmed alternate histologies other than renal cell carcinoma in each case. These data suggest that the loss of genetic material on the short arm of chromosome 3 may be specific for nonpapillary renal cell carcinoma. Molecular analysis may prove to be a useful adjunct in establishing the diagnosis in renal neoplasms with equivocal histologies.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Adult
  • Alleles
  • Carcinoma, Ductal, Breast / diagnosis*
  • Carcinoma, Ductal, Breast / genetics
  • Carcinoma, Renal Cell / diagnosis*
  • Carcinoma, Renal Cell / genetics
  • Carcinoma, Renal Cell / surgery
  • Chromosome Aberrations / genetics
  • Chromosomes, Human, Pair 11
  • Chromosomes, Human, Pair 17
  • Chromosomes, Human, Pair 3
  • DNA Probes / analysis*
  • Diagnosis, Differential
  • Female
  • Genetic Carrier Screening
  • Humans
  • Kidney Neoplasms / diagnosis*
  • Kidney Neoplasms / genetics
  • Kidney Neoplasms / surgery
  • Male
  • Middle Aged
  • Molecular Biology
  • Nephrectomy
  • Peptide Fragments
  • Polymorphism, Restriction Fragment Length
  • Sarcoma / diagnosis*
  • Sarcoma / genetics

Substances

  • DNA Probes
  • Peptide Fragments