[Multiple facial squamous cell carcinomas in a child, revealing a xeroderma pigmentosum]

Rev Stomatol Chir Maxillofac. 2012 Feb;113(1):50-2. doi: 10.1016/j.stomax.2011.10.007. Epub 2011 Nov 5.
[Article in French]

Abstract

Background: Squamous cell carcinoma of the skin is very rare in children. One of its most common risk factors is xeroderma pigmentosum (XP), an autosomal recessive disease characterized by defective cellular DNA repair, and hypersensitivity to ultraviolet radiation.

Case report: We report a case of XP in a 7-year-old black African boy, revealed by squamous cell carcinomas of the inferior lip and upper left eyelid.

Discussion: In sub-Saharan regions, the early diagnosis of XP is difficult because of its uncommon occurrence on black skin and black skin specificities. The strong sun radiation in the tropics and a late diagnosis make XP treatment challenging. Thus, prevention in patients' families is mandatory.

Publication types

  • Case Reports
  • English Abstract

MeSH terms

  • Burkina Faso
  • Carcinoma, Squamous Cell / diagnosis*
  • Carcinoma, Squamous Cell / etiology
  • Carcinoma, Squamous Cell / pathology
  • Child
  • Diagnosis, Differential
  • Facial Neoplasms / diagnosis*
  • Facial Neoplasms / etiology
  • Facial Neoplasms / pathology
  • Humans
  • Male
  • Skin Neoplasms / diagnosis*
  • Skin Neoplasms / etiology
  • Skin Neoplasms / pathology
  • Xeroderma Pigmentosum / complications
  • Xeroderma Pigmentosum / diagnosis*
  • Xeroderma Pigmentosum / pathology