Langerhans cell histiocytosis: a diagnostic dilemma

Paul L Ryan, Kim M Piper, Francis J Hughes

Research output: Contribution to journalArticlepeer-review

4 Citations (Scopus)

Abstract

Langerhans cell histiocytosis (LCH) is a rare clonal neoplastic disorder of unknown aetiology which can present with a diverse range of clinical presentations. It encompasses a diverse number of idiopathic conditions which can involve multiple body systems and is characterized by bone marrow-derived Langerhans cell proliferation. The disease can affect multiple body systems and lesions can be solitary or widespread. We present a case of a multifocal eosinophilic granuloma (LCH) in a young adult female with clinical signs and symptoms similar to aggressive periodontitis. Clinical Relevance: Langerhans cell histiocytosis is a rare disease which can have a similar clinical presentation to aggressive periodontitis.
Original languageEnglish
Article numberN/A
Pages (from-to)716-8, 720
Number of pages4
JournalDental Update
Volume39
Issue number10
Publication statusPublished - Dec 2012

Keywords

  • Adult
  • Aggressive Periodontitis
  • Diagnosis, Differential
  • Eosinophilic Granuloma
  • Female
  • Histiocytosis, Langerhans-Cell
  • Humans
  • Mandibular Neoplasms

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