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Papillary glioneuronal tumor: A rare case with recent updates as per 2021 CNS WHO 5th classification.
Mehrotra, Bandana; Bhargav, Mithlesh; Kapoor, Ashok; Pandey, Shubhi; Brij, Saumya; Gopal, Vaibhav R.
Affiliation
  • Mehrotra B; MD Pathology, RML Laboratory, Lucknow, Uttar Pradesh, India.
  • Bhargav M; MD Pathology, RML Laboratory, Lucknow, Uttar Pradesh, India.
  • Kapoor A; MD Pathology, RML Laboratory, Lucknow, Uttar Pradesh, India.
  • Pandey S; MD Pathology, RML Laboratory, Lucknow, Uttar Pradesh, India.
  • Brij S; MD Pathology, RML Laboratory, Lucknow, Uttar Pradesh, India.
  • Gopal VR; MS Surgery, RMLIMS, Lucknow, Uttar Pradesh, India.
Article in En | MEDLINE | ID: mdl-38427744
ABSTRACT
ABSTRACT 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.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Indian J Pathol Microbiol Year: 2024 Document type: Article Affiliation country: India Country of publication: India

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Indian J Pathol Microbiol Year: 2024 Document type: Article Affiliation country: India Country of publication: India