Langerhans Cell Histiocytosis of the Oral Mucosa: A Rare Case Report

Journal Title: International Journal of Health Sciences and Research - Year 2017, Vol 7, Issue 1

Abstract

Langerhans cell histiocytosis (LCH) is a rare idiopathic disease characterized by the clonal proliferation of bone marrow derived Langerhans cells. It usually occurs in children. Their clinical features simulate common oral findings such as gingival enlargement, oral ulcers, and mobility of teeth, along with nonspecific radiographic features, thus easily leading to the misdiagnosis and therefore, it could be overlooked by dentists. We report a rare case of LCH in 38‑year‑old adult male, characterized by oral mucosal ulcerations with no involvement of the underlying bone. The lesion was histologically proven to be LCH and was confirmed with immunohistochemical staining of S100 protein and CD1a antigen.

Authors and Affiliations

Mounir Omami

Keywords

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  • EP ID EP368121
  • DOI -
  • Views 91
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How To Cite

Mounir Omami (2017). Langerhans Cell Histiocytosis of the Oral Mucosa: A Rare Case Report. International Journal of Health Sciences and Research, 7(1), 291-296. https://www.europub.co.uk/articles/-A-368121