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Title

Isolated intracranial Rosai-Dorfman disease in an adult man: Report of a rare case

Pages

  0-0

Abstract

 Background: Isolated Intracranial Rosai-Dorfman Disease (RDD) is an extremely rare, idiopathic Histo-proliferative disorder. RDD is associated with the proliferation of histiocytes and Emperipolesis. Case Presentation: we report a case with isolated Intracranial RDD. A 47-year-old man presented with a dizziness, falling, and then secondary generalized seizure, hemiparesis and right hemisensory deficit. This case preoperatively was misdiagnosed with meningioma. Histopathological examination revealed pale histiocytes displaying Emperipolesis which were positive for S-100 and CD68 proteins and negative for CD1a marker. BRAF V600E mutation was negative. Conclusion: In this case, total resection was performed and clinical symptoms were regressed completely.

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    APA: Copy

    Rezaei, Somaye, Zarzanalivan, Fariba, Pirouti, Pouya, Amiri Nikpour, Mohammad Reza, JAVADI, ABDOLREZA, & TORKAMANDI, SHAHRAM. (2020). Isolated intracranial Rosai-Dorfman disease in an adult man: Report of a rare case. JOURNAL OF RESEARCH IN CLINICAL MEDICINE, 8(1), 0-0. SID. https://sid.ir/paper/355192/en

    Vancouver: Copy

    Rezaei Somaye, Zarzanalivan Fariba, Pirouti Pouya, Amiri Nikpour Mohammad Reza, JAVADI ABDOLREZA, TORKAMANDI SHAHRAM. Isolated intracranial Rosai-Dorfman disease in an adult man: Report of a rare case. JOURNAL OF RESEARCH IN CLINICAL MEDICINE[Internet]. 2020;8(1):0-0. Available from: https://sid.ir/paper/355192/en

    IEEE: Copy

    Somaye Rezaei, Fariba Zarzanalivan, Pouya Pirouti, Mohammad Reza Amiri Nikpour, ABDOLREZA JAVADI, and SHAHRAM TORKAMANDI, “Isolated intracranial Rosai-Dorfman disease in an adult man: Report of a rare case,” JOURNAL OF RESEARCH IN CLINICAL MEDICINE, vol. 8, no. 1, pp. 0–0, 2020, [Online]. Available: https://sid.ir/paper/355192/en

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