مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Information Journal Paper

Title

MULTICENTRIC RETICULOHISTIOCYTOSIS: A CASE REPORT

Pages

  372-379

Abstract

 Multicentric RETICULOHISTIOCYTOSIS (MRH) is a rare PROLIFERATIVE HISTIOCYTIC DISEASE of ‎unknown cause with potentially disabling nature. Primary manifestations are involvement ‎of skin and joints. The articular destruction can lead to permanent joint deformities. Our ‎patient was a 47 year-old woman with bilateral symmetrical polyarthritis and reddish- ‎brown papulonodular cutaneous lesions. The diagnosis of MULTICENTRIC RETICULOHISTIOCYTOSIS ‎was confirmed by histological examination. Both skin and articular manifestations were only ‎partially treated with oral corticosteroids, monthly bolus cyclophosphamide, weekly ‎methotrexate and knee synoviorthesis with nitrogen mustard.

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    Cite

    APA: Copy

    REZAEI YAZDI, Z., SANDOUGHI, M., MANSOURI TORGHABEH, H., & DERHAMI, A.. (2005). MULTICENTRIC RETICULOHISTIOCYTOSIS: A CASE REPORT. ACTA MEDICA IRANICA, 43(5), 372-379. SID. https://sid.ir/paper/277846/en

    Vancouver: Copy

    REZAEI YAZDI Z., SANDOUGHI M., MANSOURI TORGHABEH H., DERHAMI A.. MULTICENTRIC RETICULOHISTIOCYTOSIS: A CASE REPORT. ACTA MEDICA IRANICA[Internet]. 2005;43(5):372-379. Available from: https://sid.ir/paper/277846/en

    IEEE: Copy

    Z. REZAEI YAZDI, M. SANDOUGHI, H. MANSOURI TORGHABEH, and A. DERHAMI, “MULTICENTRIC RETICULOHISTIOCYTOSIS: A CASE REPORT,” ACTA MEDICA IRANICA, vol. 43, no. 5, pp. 372–379, 2005, [Online]. Available: https://sid.ir/paper/277846/en

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