Langerhans-cell histiocytosis: a clinical case without bone involvement.

Abstract:

BACKGROUND:Langerhans-cell histiocytosis (LCH) is a group of rare disorders histologically characterized by the proliferation of Langerhans cells. Multiple organs and systems may be involved by the disease. Typically, there is bone involvement and, less frequently, lesions may be found in the lungs, liver, lymph nodes, skin, and mucosae. Oral soft tissue lesions without bone involvement are rare. METHODS:We report a case of a 23-year-old man with LCH detected by oral soft tissue, cutaneous, and lung lesions. RESULTS:Due to the oral lesion diagnosis, important procedures were performed, which determined the staging of the disease. CONCLUSION:Gingival lesions could be one of the first manifestations of LCH. The periodontist should recognize and detect this important pathology with oral involvement.

journal_name

J Periodontol

authors

Manfredi M,Corradi D,Vescovi P

doi

10.1902/jop.2005.76.1.143

subject

Has Abstract

pub_date

2005-01-01 00:00:00

pages

143-7

issue

1

eissn

0022-3492

issn

1943-3670

journal_volume

76

pub_type

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