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Isolated Intracranial Rosai-Dorfman Disease Mimicking a Meningioma

Author

Listed:
  • Amer Alshurbaji MD
  • Alhareth Ma’aya MD
  • Faisal Alshurbaji MD
  • Wagdy Al-Kadasi MD

    (Department of Neurosurgery, King Hussein Medical Center, Jordan)

  • Duaa Alshurbaji MD

    (Department of Histopathology, King Hussein Medical Center, Jordan)

Abstract

Rosai-Dorfman disease (RDD) is a rare idiopathic his to proliferative disorder that usually presents with systemic symptoms and cervical lymphadenopathy. Intracranial involvement is relatively rare and isolated intracranial RDD is very scarce. It resembles meningioma on imaging scans and is difficult to differentiate preoperatively. We present our case of isolated intracranial RDD in 25 years-old man that mimicked a meningioma on imaging.

Suggested Citation

  • Amer Alshurbaji MD & Alhareth Ma’aya MD & Faisal Alshurbaji MD & Wagdy Al-Kadasi MD & Duaa Alshurbaji MD, 2017. "Isolated Intracranial Rosai-Dorfman Disease Mimicking a Meningioma," Open Access Journal of Neurology & Neurosurgery, Juniper Publishers Inc., vol. 5(2), pages 17-19, July.
    • Handle: RePEc:adp:joajnn:v:5:y:2017:i:2:p:17-19
    DOI: 10.19080/OAJNN.2017.05.555656
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