Background: Gangliogliomas (GGs) are rare intra-axial tumors. Cerebellar seizures caused by GGs have been described only rarely. Pigmented neural cell tumors are well described in the literature but are infrequent, especially when presenting as primary neuroepithelial tumors. Only 5 cases of pigmented GG have been reported previously, including 4 in the pediatric population.
Case Description: A 17-year-old female presented to us with cerebellar seizures, which resolved after tumor excision. Histopathological examination revealed a pigmented GG.
Conclusions: We present the sixth documented case of a pigmented ganglioglioma, the first such case reported in cerebellar location, associated with a rare presentation of cerebellar seizures.
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| http://dx.doi.org/10.1016/j.wneu.2018.04.219 | DOI Listing |
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