Isolated Intracranial Rosai-Dorfman Disease Mimicking a Meningioma

Amer Alshurbaji Md, Alhareth Ma’aya Md, Faisal Alshurbaji Md, Wagdy Al-Kadasi Md and Duaa Alshurbaji Md
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Wagdy Al-Kadasi Md: Department of Neurosurgery, King Hussein Medical Center, Jordan
Duaa Alshurbaji Md: Department of Histopathology, King Hussein Medical Center, Jordan

Open Access Journal of Neurology & Neurosurgery, 2017, vol. 5, issue 2, 17-19

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.

Keywords: Open Access Journal of Neurology; Journal of Neurology & Neurosurgery; Open Access Journal; juniper publishers; neurology open access journals; journal of neurology; neurology indexed journals; neurology scholarly journals; journal of neurology; neurology journals impact factor; juniper publishers reivew (search for similar items in EconPapers)
Date: 2017
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Persistent link: https://EconPapers.repec.org/RePEc:adp:joajnn:v:5:y:2017:i:2:p:17-19

DOI: 10.19080/OAJNN.2017.05.555656

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