Evidence map›Paper›PMID 42722904›Full record

ArticleChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2026

Pediatric low-grade glial, glioneuronal and neuronal tumors: a retrospective study of 85 cases.

Meriem Boubekri, Nadia Cherradi

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Article in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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2 authors.

Meriem BoubekriPathology Department, Specialties Hospital, Ibn Sina University Hospital, Mohammed V University in Rabat, Avenue Abderrahim Bouabid, Rabat, 10000, Morocco. meriem_boubekri@um5.ac.ma.ORCID 0009-0007-8112-5807
Nadia CherradiPathology Department, Specialties Hospital, Ibn Sina University Hospital, Mohammed V University in Rabat, Avenue Abderrahim Bouabid, Rabat, 10000, Morocco.

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6 · The paper itself

Abstract

purposePediatric low-grade glial, glioneuronal, and neuronal tumors are the most prevalent solid tumors in children, accounting for more than one-third of all pediatric brain tumors. These tumors exhibit a wide range of clinicopathological characteristics. This study aimed to define the epidemiological and clinicopathological profile of these tumors based on the experience of the Pathology Department of the Specialties Hospital of Ibn Sina University Hospital in Rabat.

methodsA retrospective descriptive study was conducted on 85 cases of low-grade glial, glioneuronal, and neuronal tumors in patients aged ≤ 18 years at the Pathology Department of the Specialties Hospital of Ibn Sina University Hospital in Rabat over a period of 10 years (2016-2025).

resultsThe mean age of the patients was 10 years, and there was a slight male predominance. The most common clinical presentation was intracranial hypertension, observed in 59 cases (69%). Supratentorial locations were identified in 49 cases (57.6%). Neuroimaging using MRI identified both cystic and solid components in 61 cases. Histopathological examination identified pilocytic astrocytoma as the most common tumour entity (61/85 cases, 71.7%), followed by ganglioglioma (10/85 cases, 11.7%) and dysembryoplastic neuroepithelial tumour (5/85 cases, 6%). Subependymal giant cell astrocytoma and pleomorphic xanthoastrocytoma were each diagnosed in two cases (2.3%). Angiocentric glioma, polymorphous low-grade neuroepithelial tumor of the young, central neurocytoma, extraventricular neurocytoma, and pilomyxoid astrocytoma were each identified in one case (1.2%).

conclusionPediatric low-grade glial, glioneuronal, and neuronal tumors are a heterogeneous group with distinct clinicopathological features. This study defines their profile at our institution and supports the need for larger multicenter studies.

Indexed as

Brain NeoplasmsGliomaAdolescentChildChild, PreschoolFemaleHumansInfantMaleRetrospective StudiesChildrenCNSMolecular biologyNeuropathologyWHO

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