Clinicopathological and molecular study of penile melanoma

J Clin Pathol. 2012 Mar;65(3):228-31. doi: 10.1136/jclinpath-2011-200344. Epub 2011 Oct 19.

Abstract

Aims: To examine the clinicopathological features of a series of penile melanomas and screen for mutations in the BRAF and KIT genes, which are seen in melanomas from other sites.

Methods and results: 12 patients with penile melanoma were identified over a 10-year period in two supra-regional networks in the UK. The 2- and 5-year survival was 61% and 20%, respectively. Half the patients had lymph node involvement at presentation; this was a poor prognostic indicator. KIT exons 11, 13, 17 and 18, and BRAF codons 600 and 601 were analysed for mutations by Sanger sequencing and pyrosequencing, respectively. None of the tumours showed either KIT mutations or the BRAF V600E mutation.

Conclusion: Penile melanomas are extremely rare and have a similar prognosis to melanomas elsewhere, but they often present late, leading to a poor outcome. The mutations seen in melanomas from other sites appear to be rarely present in these tumours.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Codon
  • DNA Mutational Analysis
  • Exons
  • Genetic Predisposition to Disease
  • Humans
  • Kaplan-Meier Estimate
  • Lymphatic Metastasis
  • Male
  • Melanoma / genetics*
  • Melanoma / mortality
  • Melanoma / secondary
  • Melanoma / therapy
  • Middle Aged
  • Mutation*
  • Penile Neoplasms / genetics*
  • Penile Neoplasms / mortality
  • Penile Neoplasms / pathology
  • Penile Neoplasms / therapy
  • Phenotype
  • Prognosis
  • Proto-Oncogene Proteins B-raf / genetics*
  • Proto-Oncogene Proteins c-kit / genetics*
  • Skin Neoplasms / genetics*
  • Skin Neoplasms / mortality
  • Skin Neoplasms / pathology
  • Skin Neoplasms / therapy
  • Survival Rate
  • Time Factors
  • United Kingdom

Substances

  • Codon
  • Proto-Oncogene Proteins c-kit
  • BRAF protein, human
  • Proto-Oncogene Proteins B-raf