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Cites:

Information Journal Paper

Title

LANGERHANCE CELL HISTIOCYTOSIS WITH PRIMARY ORAL MANIFESTATIONS; A CASE STUDY

Pages

  347-352

Abstract

 Introduction: HISTIOCYTOSIS of the langerhans cell is a rare disorder with unknown etiology and a spectrum of disorders characterized by proliferation of the histiocyte-like cells. It presents as Eosinophilic granuloma, Handschuller Christian disease, and Letter-siwe disease. The incidence rate is 2.1 in 200.000 child per year.Case Report: The patient was a 3.5 year old male child reffered with swelling of the gingival and hypermobility of the deciduous molar teeth. The diagnostic procedures until the final diagnosis of LANGERHANCE CELL HISTIOCYTOSIS and treatment of this case are reported.Conclusion: Oral lesions could be the first manifestion of HISTIOCYTOSIS of the langerhans cell, of which the dentists should be aware. The early diagnosis is so important in treatment and survival of the patient.

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  • Cite

    APA: Copy

    GHALYANI, P., SARRAFAN, N., & PISHVA, S.. (2011). LANGERHANCE CELL HISTIOCYTOSIS WITH PRIMARY ORAL MANIFESTATIONS; A CASE STUDY. JOURNAL OF DENTISTRY (SHIRAZ UNIVERSITY OF MEDICAL SCIENCES), 11(4 (29)), 347-352. SID. https://sid.ir/paper/108665/en

    Vancouver: Copy

    GHALYANI P., SARRAFAN N., PISHVA S.. LANGERHANCE CELL HISTIOCYTOSIS WITH PRIMARY ORAL MANIFESTATIONS; A CASE STUDY. JOURNAL OF DENTISTRY (SHIRAZ UNIVERSITY OF MEDICAL SCIENCES)[Internet]. 2011;11(4 (29)):347-352. Available from: https://sid.ir/paper/108665/en

    IEEE: Copy

    P. GHALYANI, N. SARRAFAN, and S. PISHVA, “LANGERHANCE CELL HISTIOCYTOSIS WITH PRIMARY ORAL MANIFESTATIONS; A CASE STUDY,” JOURNAL OF DENTISTRY (SHIRAZ UNIVERSITY OF MEDICAL SCIENCES), vol. 11, no. 4 (29), pp. 347–352, 2011, [Online]. Available: https://sid.ir/paper/108665/en

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