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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Detaylı Bibliyografya
Yayımlandı:Medicine (Baltimore)
Asıl Yazarlar: Yang, Xiang, Liu, Jiagang, Ren, Yanming, Richard, Seidu A., Zhang, Yuekang
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Wolters Kluwer Health 2017
Konular:
5300
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5708970/
https://ncbi.nlm.nih.gov/pubmed/29381971
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000008754
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