[Langerhans cell histiocytosis]

Rev Stomatol Chir Maxillofac. 2009 Nov;110(5):287-9. doi: 10.1016/j.stomax.2009.07.008. Epub 2009 Oct 13.
[Article in French]

Abstract

Langerhans cell histiocytosis (ex histiocytosis X) is usually present in children. It is a clonal proliferation of non-functional Langerhans's cells. Histological aspects are variable. The diagnosis is made in immunolabeling by anti-CD1a. Clinical presentations are variable, depending on their extension. Three syndromes are actually the same pathogenic process: eosinophilic granuloma (single or multiple osseous localizations), Hand-Schüller-Christian disease (chronic form with bone and visceral dissemination) and Abt-Letterer-Siwe disease (disseminated and acute malignant presentation).

Publication types

  • English Abstract
  • Review

MeSH terms

  • Histiocytosis, Langerhans-Cell / classification*
  • Histiocytosis, Langerhans-Cell / pathology*
  • Humans