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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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| Publicat a: | Medicine (Baltimore) |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Wolters Kluwer Health
2017
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| Matèries: | |
| Accés en línia: | 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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