Background: Pediatric cerebral ganglioneuroblastoma is an exceedingly rare tumor.
Case Description: We describe the case of a 4-year-old boy with sudden mental status decline who was found to have a large intracranial lesion with intraventricular extension.
Conclusion: Management of the case and pathologic findings are discussed, along with a review of the literature on this rare entity.
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http://dx.doi.org/10.1016/j.wneu.2018.02.115 | DOI Listing |
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