[CDKN2A gene mutation and loss of p16 protein activity in a patient on levodopa presenting sporadic multiple primary melanoma]

Ann Dermatol Venereol. 2006 Oct;133(10):777-80. doi: 10.1016/s0151-9638(06)71042-0.
[Article in French]

Abstract

Background: Cutaneous melanoma is a complex disease involving genetic and environmental factors. Levodopa has been incriminated in the development and/or progression of melanoma.

Observation: We report the case of a man treated with levodopa and a dopadecarboxylase inhibitor for Parkinson's disease and presenting 22 cutaneous melanomas over a 4-year period. The patient is of phototype II and presents multiple nevi. Genetic analysis of predisposing genes demonstrated a CDKN2A mutation with loss of p16 activity.

Discussion: Multiple melanomas may be associated with genetic predisposition, and screening for the latter should be performed. The exceptionally high number of melanomas developed by our patient raised suspicions about levodopa, a precursor in melanin synthesis, as a potential inducer. Increased dermatologic controls and screening for predisposing genetic factors appear to us to be warranted in the event of melanoma development in patients on levodopa.

Publication types

  • Case Reports
  • English Abstract

MeSH terms

  • Antiparkinson Agents / adverse effects*
  • Cyclin-Dependent Kinase Inhibitor p16 / physiology*
  • Genes, p16*
  • Humans
  • Levodopa / adverse effects*
  • Male
  • Melanoma / chemically induced*
  • Melanoma / genetics*
  • Middle Aged
  • Mutation*
  • Skin Neoplasms / chemically induced*
  • Skin Neoplasms / genetics*

Substances

  • Antiparkinson Agents
  • Cyclin-Dependent Kinase Inhibitor p16
  • Levodopa