A Rare Case of Isolated Intracranial Rosai–Dorfman Disease Mimicking Optic Nerve Meningioma: A Case Report and Literature Review

Autor: Srour Robin, Hani Talal Aljohani
Jazyk: angličtina
Rok vydání: 2018
Předmět:
Zdroj: Asian Journal of Neurosurgery
ISSN: 2248-9614
1793-5482
Popis: Sinus histiocytosis with massive lymphadenopathy, or Rosai–Dorfman disease (RDD), was first described in 1969 as a reactive condition of unknown etiology that is characterized by a proliferation of histiocytes exhibiting emperipolesis of both lymphocytes and plasma cells. It usually presents with painless cervical lymphadenopathy either with or without extranodal manifestations. Intracranial involvement of this disease is extremely rare. Intracranial RDD occurs in
Databáze: OpenAIRE
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