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Cites:

Information Journal Paper

Title

LANGERHANCE CELL HISTIOCYTOSIS WITH PRIMARY CUTANEOUS AND ORAL MANIFESTATIONS

Pages

  82-88

Abstract

 Introduction: HISTIOCYTOSIS of lagerhans cell is a spectrum of disorders characterized by proliferation of Histiocyte like cells and includes following: Eosinophilic granuloma, Hand– Schuller Christian disease and Letterer- Siwe disease. The incidence is 0.5 in 100000 person per year in individuals younger than 15 years old.Case Report: The patient was a 57 day old male infant referred with papulovesicular cutaneous and exophitic oral lesions without bone and visceral involvement. Diagnostic procedures until final diagnosis of LANGERHANCE CELL HISTIOCYTOSIS and treatment of this case have been reported.Conclusion: Oral lesions could be the first manifestation of disease and dentists should be aware of that. According to different investigations, the disease may have a genetic basis.

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  • Cite

    APA: Copy

    GHALYANI, P., TAVANGAR, S.M., & AMINZADEH, ATOUSA. (2007). LANGERHANCE CELL HISTIOCYTOSIS WITH PRIMARY CUTANEOUS AND ORAL MANIFESTATIONS. JOURNAL OF ISFAHAN DENTAL SCHOOL, 3(2), 82-88. SID. https://sid.ir/paper/126610/en

    Vancouver: Copy

    GHALYANI P., TAVANGAR S.M., AMINZADEH ATOUSA. LANGERHANCE CELL HISTIOCYTOSIS WITH PRIMARY CUTANEOUS AND ORAL MANIFESTATIONS. JOURNAL OF ISFAHAN DENTAL SCHOOL[Internet]. 2007;3(2):82-88. Available from: https://sid.ir/paper/126610/en

    IEEE: Copy

    P. GHALYANI, S.M. TAVANGAR, and ATOUSA AMINZADEH, “LANGERHANCE CELL HISTIOCYTOSIS WITH PRIMARY CUTANEOUS AND ORAL MANIFESTATIONS,” JOURNAL OF ISFAHAN DENTAL SCHOOL, vol. 3, no. 2, pp. 82–88, 2007, [Online]. Available: https://sid.ir/paper/126610/en

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