Isolated intracranial Rosai–Dorfman disease mimicking petroclival meningioma in a child: Case report and review of the literature

RATIONALE: Rosai –Dorfman disease (RDD) is a rare, idiopathic, and non-neoplastic histioproliferative disease with distinctive entity of unknown etiology. Central nervous system (CNS) RDD is uncommon, hence, isolated intracranial RDD is extremely rare. So far only 6 cases of CNS RDD with the lesions...

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Detalles Bibliográficos
Autores principales: Yang, Xiang, Liu, Jiagang, Ren, Yanming, Richard, Seidu A., Zhang, Yuekang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2017
Materias:
5300
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5708970/
https://www.ncbi.nlm.nih.gov/pubmed/29381971
http://dx.doi.org/10.1097/MD.0000000000008754

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5708970/
https://www.ncbi.nlm.nih.gov/pubmed/29381971
http://dx.doi.org/10.1097/MD.0000000000008754

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