ArticleRadiology case reports2019
A case of a rosette-forming glioneuronal tumor arising from the pons with disappearance of contrast enhancement.
Article in Radiology case reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed.
- The Clinical and Molecular Landscape of Rosette-Forming Glioneuronal Tumors.Biomedicines · 2024Review
- Clinicopathological analysis of rosette-forming glioneuronal tumors.Diagnostic pathology · 2024Review
- Rosette-forming glioneuronal tumours: two case reports and a review of the literature.BJR case reports · 2022Article
- Pediatric rosette-forming glioneuronal tumor of the septum pellucidum.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2020Article
- Rosette-forming glioneuronal tumor: an illustrative case and a systematic review.Neuro-oncology advancesReview
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Authors and funding
9 authors.
Funding
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Abstract
A rosette-forming glioneuronal tumor (RGNT) is a rare and slow-growing central nervous system tumor. This tumor is usually assessed by MRI during the follow-up period. RGNT can show alteration of contrast enhancement regardless of tumor growth. Here, we report a case of RGNT arising from pons which shows partial enhancement on initial MRI, smaller enhancement on follow-up MRI at 10 months, and totally disappeared at 18 months without any therapy.
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