The papillary glioneuronal tumor is a WHO grade 1, rare neuronal-glial tumor and comprises 0.02% of all CNS tumors. Histologically, it is a mixture of glial and neuronal components showing a pseudopapillary pattern with hyalinized vessels. PGNT is considered a low-grade neoplasm, and surgical excision has been curative in most cases. In this paper, we report a new case of papillary glioneuronal tumor in a 44-year-old male having a divergent presentation, to analyze it due to the rarity of its occurrence as per the latest classification.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.4103/ijpm.ijpm_310_23 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!