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Cites:

Information Journal Paper

Title

LANGERHANS CELL HISTIOCYTOSIS: A CASE REPORT

Pages

  132-136

Abstract

LANGERHANS CELL HISTIOCYTOSIS (LCH) is a proliferative disorder of langerhans cells and lymphocytes having different subtypes and a wide range of clinical manifestations and severity ranging from a unifocal self-limited disorder to multi-system involvement and even death. Along with clinical manifestations, diagnosis is made through existence of specific IMMUNOHISTOCHEMISTRY markers. Where treatment is necessary, different treatment modalities have been proposed; though none have found to be optimal.this paper introduces a 23-year old girl with an extensive yellowish to red-brown MACULOPAPULAR rash over her face accompanied with polyuria, polydipsia, and fatigue.

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  • Cite

    APA: Copy

    ZARTAB, HAMED, PAZHOUHI, NEDA, & NASSIRI KASHANI, MANSOUR. (2011). LANGERHANS CELL HISTIOCYTOSIS: A CASE REPORT. DERMATOLOGY AND COSMETIC, 2(2), 132-136. SID. https://sid.ir/paper/157625/en

    Vancouver: Copy

    ZARTAB HAMED, PAZHOUHI NEDA, NASSIRI KASHANI MANSOUR. LANGERHANS CELL HISTIOCYTOSIS: A CASE REPORT. DERMATOLOGY AND COSMETIC[Internet]. 2011;2(2):132-136. Available from: https://sid.ir/paper/157625/en

    IEEE: Copy

    HAMED ZARTAB, NEDA PAZHOUHI, and MANSOUR NASSIRI KASHANI, “LANGERHANS CELL HISTIOCYTOSIS: A CASE REPORT,” DERMATOLOGY AND COSMETIC, vol. 2, no. 2, pp. 132–136, 2011, [Online]. Available: https://sid.ir/paper/157625/en

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