ReviewChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2011
Glioblastoma multiforme with very rapid growth and long-term survival in children: report of two cases and review of the literature.
Review in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 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
7 citing papers in PubMed.
- Within five weeks: Rapidly grown glioblastoma discovered on repeat MRI after pathologic EEG.Clinical neurophysiology practice · 2025Article
- Comprehensive analysis of Iranian reports of pediatric central nervous system tumors.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2017Article
- Pediatric glioblastoma: a single institution experience.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2016Article
- BUB1 and BUBR1 inhibition decreases proliferation and colony formation, and enhances radiation sensitivity in pediatric glioblastoma cells.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2013Article
- Polo-like kinase 1 inhibition causes decreased proliferation by cell cycle arrest, leading to cell death in glioblastoma.Cancer gene therapy · 2013Article
- Cell surface markers of cancer stem cells: diagnostic macromolecules and targets for drug delivery.Drug delivery and translational research · 2013Article
- Glioblastoma Shortly after a Normal Conventional Brain Magnetic Resonance Imaging: A Report of Two Cases and Review of the Literature.Asian journal of neurosurgeryArticle
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3 authors.
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No grant is acknowledged in the PubMed record.
Abstract
Glioblastoma occurs rarely in pediatric patients (0.6-7.9% of all glioblastomas). Symptom duration is about 3-5 months prior to diagnosis with a dismal prognosis (median survival of 50 weeks). The authors describe two pediatric age patients with histopathologically confirmed glioblastoma multiforme whose lesions appeared within just 1 week of normal computed tomography scan and magnetic resonance imaging. Both patients had long-term survival (one of them 6 years and the other 3 years and 7 months) following tumor resection. The present report serially illustrates the very rapid development of glioblastoma in childhood and emphasizes the importance of serial neuroimaging as well as paying attention to sudden onset headaches in pediatric patients with inconclusive imaging findings.
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Registered trials
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