Huriez syndrome: Case report with a detailed analysis of skin dendritic cells

C. Guerriero, C. Albanesi, G. Girolomoni, C. De Simone, R. Capizzi, P. Amerio, A. Tulli

Research output: Contribution to journalArticle

Abstract

We report a 60-year-old man with familial scleroatrophic syndrome of Huriez who developed squamous cell carcinomas on the affected skin of the right palm. Immunohistochemical analysis showed a marked reduction in the number of CD1a+, Lag+ and S100+ epidermal Langerhans cells, but not of CD1b+ and factor XIIIa+ dermal dendritic cells, limited to palmoplantar skin. The Langerhans cell depletion was not associated with an abnormal skin content of mRNA for factors involved in Langerhans cell development or recruitment in the epidermis, including granulocyte/macrophage colony-stimulating factor, transforming growth factor-β1 and macrophage inflammatory protein-3α. The results indicate that other as yet unknown mechanisms may account for the reduced number of Langerhans cells in the affected skin of such patients.

Original languageEnglish
Pages (from-to)1091-1096
Number of pages6
JournalBritish Journal of Dermatology
Volume143
Issue number5
DOIs
Publication statusPublished - 2000

    Fingerprint

Keywords

  • Huriez syndrome
  • Immunohistochemistry
  • Langerhans cells
  • Squamous cell carcinoma

ASJC Scopus subject areas

  • Dermatology

Cite this

Guerriero, C., Albanesi, C., Girolomoni, G., De Simone, C., Capizzi, R., Amerio, P., & Tulli, A. (2000). Huriez syndrome: Case report with a detailed analysis of skin dendritic cells. British Journal of Dermatology, 143(5), 1091-1096. https://doi.org/10.1046/j.1365-2133.2000.03793.x