ArticleCureus2024
Cerebellar Glioblastoma: A Literature Review and Case Analysis.
Article in Cureus, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed, 2 citations in OpenAlex.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Glioblastoma multiforme is one of the most common primary intracranial tumors with a particularly aggressive behavior. It usually develops in the cerebral hemispheres, with infratentorial localization being extremely rare. If located in the posterior cranial fossa, glioblastoma most often presents with symptoms of increased intracranial pressure and impaired cerebellar function. In this article, we present a case of small-cell glioblastoma, which is a rare histological variant of this type of high-grade glioma, situated in the cerebellum. A 31-year-old woman was admitted to the neurosurgery department with severe headache, impaired balance, and weakness in the right arm. Magnetic resonance imaging of the brain showed evidence of a lesion with solid and cystic components in the right cerebellar hemisphere. The latter was surgically removed and the histological examination determined the diagnosis of cerebellar small-cell glioblastoma. The treatment of this patient included a combined approach, i.e., radiotherapy and chemotherapy with temozolomide after surgery. Follow-up for a period of more than two years was done and the patient showed no significant clinical symptoms. There was no evidence of recurrence on follow-up imaging studies.
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Registered trials
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.