ReviewChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2016
Rosette-forming glioneuronal tumor outside the fourth ventricle: a case-based update.
Review in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
9 citing papers in PubMed.
- A Rare Lesion in the Anterior Region of the Third Ventricle: Rosette-Forming Glioneuronal Tumor.Cureus · 2024Article
- Molecular characterization of gliomas and glioneuronal tumors amid Noonan syndrome: cancer predisposition examined.Frontiers in oncology · 2024Article
- Article
- 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 update.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2020Review
- Rosette-forming glioneuronal tumour of the fourth ventricle. Not always a foreseeable development.Contemporary oncology (Poznan, Poland) · 2018Article
- Freiburg Neuropathology Case Conference: A Cystic Lesion of the Cerebellum in an Adolescent.Clinical neuroradiology · 2017Article
- Rosette-forming glioneuronal tumor: an illustrative case and a systematic review.Neuro-oncology advancesReview
Corrections and comments
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
introductionRosette-forming glioneuronal tumors (RGNTs) that do not involve the fourth ventricle are rare. RGNTs were originally thought to be exclusively localized into the fourth ventricle but were found in various anatomical localizations. MATERIAL AND
methodsWe review the literature and found 32 cases of this particular RGNT. The outcome was excellent with no mortality reported after surgical treatment. Only two patients had received adjuvant therapy for progression. We added one case of a RGNT located in the cerebellar hemisphere. CASE AND
conclusionShe underwent a subtotal removal with no evidence of progression after. This WHO grade I tumor with a specific biphasic histopathology is of a good oncological outcome after surgical treatment. A long follow-up is needed as recurrence or metastatic progressions exist.
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