An update on clonality, cytokines, and viral etiology in Langerhans cell histiocytosis

C. L. Willman, K. L. McClain

Research output: Contribution to journalArticlepeer-review

Abstract

Many etiologies have been proposed for Langerhans cell histiocytosis (LCH). Recent scientific studies have clearly provided new insights into the etiology and pathogenesis of the disease. The possible role of viruses has not been completely negated, but no viral genomes have been consistently detected in LCH lesions. Other studies do not indicate that LCH arises from a primary defect in the immune system, although altered immune responses and immune dysfunction may play a role in the pathophysiology of the disease. Definitive results have been gained from molecular studies of clonality, however. These have definitively established that LCH is a clonal histiocytic disease rather than a reactive polyclonal disorder.

Original languageEnglish (US)
Pages (from-to)407-416
Number of pages10
JournalHematology/Oncology Clinics of North America
Volume12
Issue number2
DOIs
StatePublished - 1998

ASJC Scopus subject areas

  • Hematology
  • Oncology

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