Primary isolated intracranial Rosai–Dorfman disease: Report of a rare case and review of the literature

ConclusionPrimary intracranial RDD, especially located in the cranial base, is exceptionally rare, which hard to be distinguished with meningoma by imageology and clinical manifestations, but could be diagnosed by pathological and immunohistochemical examinations. Surgery is of the most importance treatment and prognosis is optimistic for this disease.
Source: Polish Journal of Neurology and Neurosurgery - Category: Neurosurgery Source Type: research