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 |
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Jazyk: | angličtina |
Rok vydání: | 2018 |
Předmět: |
Pathology
medicine.medical_specialty business.industry Sinus Histiocytosis with Massive Lymphadenopathy Rosai–Dorfman disease Case Report General Medicine sinus histiocytosis medicine.disease optic nerve meningioma Intracranial tumor Meningioma Extranodal Disease Emperipolesis 03 medical and health sciences 0302 clinical medicine Cervical lymphadenopathy 030220 oncology & carcinogenesis Optic nerve Medicine medicine.symptom business 030217 neurology & neurosurgery Histiocyte |
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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