Rapid, de novo development of isolated intracranial rosai-dorfman disease: A case report

Matthew R. ReynoldsDepartment of Neurological Surgery, Washington University in St. Louis, St. Louis, MO, USA;Department of Neurological Surgery, National Centre for Neurosurgery, Beaumont Hospital, Dublin, Republic of IrelandCorrespondence[email protected]

Kieron J. SweeneyDepartment of Neurological Surgery, National Centre for Neurosurgery, Beaumont Hospital, Dublin, Republic of Ireland

Shane M. CrillyDepartment of Neurological Surgery, National Centre for Neurosurgery, Beaumont Hospital, Dublin, Republic of Ireland

Michael FarrellDepartment of Neuropathology, National Centre for Neurosurgery, Beaumont Hospital, Dublin, Republic of Ireland

Elaine S. JaffeDepartment of Pathology, National Institute of Health, National Cancer Institute, Bethesda, MD, USA

Mohsen JavadpourDepartment of Neurological Surgery, National Centre for Neurosurgery, Beaumont Hospital, Dublin, Republic of Ireland

References

Rosai J, Dorfman R. Sinus histiocytosis with massive lymphadenopathy: a newly recognized benign clinicopathological entity. Arch Pathol 1969;87:63–70.
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Symss NP, Cugati G, Vasudevan MC, Ramamurthi R, Pande A. Intracranial Rosai Dorfman disease: report of three cases and literature review. Asian J Neurosurg 2010;5:19.
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Di Rocco F, Garnett MR, Puget S, et al. Cerebral localization of Rosai–Dorfman disease in a child: Case report. J Neurosurg 2007;107:147–51.
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Rapid, de novo development of isolated intracranial rosai-dorfman disease: A case report

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Rapid, de novo development of isolated intracranial rosai-dorfman disease: A case report

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