L’histiocytose X de l’adulte est rare. Il faut savoir l’évoquer devant des lacunes osseuses cerclées d’un liseré d’autant qu’il existe des extensions dans les. Request PDF on ResearchGate | On Dec 31, , J. Corouge and others published Histiocytose X. Download Citation on ResearchGate | Histiocytose X: à propos d’un cas | Langherans’ cell histiocytosis is rare in adults. It should be considered in patients with.

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L’HL est une maladie rare.

Langerhan’s cell histiocytosis is defined as an abnormal proliferation of Hietiocytose cells in various organs and tissues bone, skin, lymph nodes The aim of this report is to review the characteristic features of this disease, the current means of diagnosis and treatment through two case reports.

The diagnosis was confirmed by histological examination of the biopsy specimen.

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The first patient underwent surgical resection of the tumor. No recurrence was observed.


In the second patient, the postoperative course was marked by the appearance of an inflammatory phenomenon in the adjacent skin and mucosa, successfully treated by intralesional corticosteroid therapy. Langerhan’s cell histiocytosis is a rare disease. The radiological appearance is also variable; histological proof is required for diagnosis.

Treatment depends on the number and locations of the lesions. For multiples locations, chemotherapy is indicated. Mandibular Langerhans cell hitiocytosis.

Langerhans cell histiocytosis – Wikipedia

Histiocytose XCellules de LangerhansMaxillaires. HistiocytosisLangerhans cellMaxillary. Journal page Archives Contents list.

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STO Histiocytose langerhansienne mandibulaire Mandibular Langerhans cell hitiocytosis.