Evidence map›Paper›PMID 40035895›Full record

ArticleChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2025

Surgical treatment of subependymal giant cell astrocytoma in patients with tuberous sclerosis complex-an institutional experience and results.

Mia Tuft, Ylva Østby Berger, Pål Bache Marthinsen, Bernt Johan Due-Tønnessen, Radek Frič

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Article in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2025. 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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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Mia TuftNational Centre for Rare Epilepsy-related Disorders, Oslo University Hospital, P.O. Box 0495, N-0424, Oslo, Norway. mia.tuft@ous-hf.no.
Ylva Østby BergerInstitute of Psychology, University of Oslo, Oslo, Norway.
Pål Bache MarthinsenDeparment of Radiology and Nuclear Medicine, Oslo University Hospital-Rikshospitalet, Oslo, Norway.
Bernt Johan Due-TønnessenDepartment of Neurosurgery, Oslo University Hospital-Rikshospitalet, Oslo, Norway.
Radek FričDepartment of Neurosurgery, Oslo University Hospital-Rikshospitalet, Oslo, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveSubependymal giant cell astrocytomas (SEGA) are present in patients with tuberous sclerosis complex (TSC), occasionally requiring surgical removal. The study aimed to analyze the results from our series of children undergoing surgery for SEGA.

methodsWe retrospectively identified children with TSC undergoing resection of SEGA at Oslo University Hospital between 1982 and 2016. Patient charts, radiological images, epilepsy, and neuropsychological reports were reviewed.

resultsOut of 208 patients with TSC, 18 (9%) underwent resection of SEGA. Due to missing data, we could only analyze results from 14 surgeries in 11 children (median age 6 years, range 0-19; male/female ratio 2.7:1). The tumours were bilateral in four (36%) patients. The tumour diameter was a median of 19 mm (10-104 mm). The surgical approach was transcortical in eight (57%) and transcallosal in six surgeries (43%). Gross total resection was achieved in 12 (86%) of surgeries. There was no mortality or major morbidity related to surgery except for one case of chronic subdural hematoma, but out of two patients with ventriculoperitoneal shunts, one developed shunt infection, and both experienced shunt failures during the follow-up. During the follow-up (median 11 years, range 1-21), three patients (27%) underwent repeated surgery. We could not document any significant impact of the surgery on patients' cognitive functioning or the grade of epilepsy.

conclusionsResection of SEGA in children with TSC was associated with a low complication rate. We could not document any impact of surgery on patients' cognitive functioning or grade of epilepsy. However, the neuropsychological data were limited in most cases. Neuropsychological assessment should be performed before the surgery and be a part of follow-up after surgery.

Indexed as

AstrocytomaBrain NeoplasmsNeurosurgical ProceduresTuberous SclerosisAdolescentChildChild, PreschoolFemaleHumansInfantInfant, NewbornMaleRetrospective StudiesTreatment OutcomeYoung AdultSubependymal giant cell astrocytomaTuberous sclerosis complex

Identifiers

PMID40035895
PMCPMC11880178

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.