Evidence map›Paper›PMID 40151500›Full record

ArticleNMC case report journal2025

A Rare Case of Giant Congenital/Infant-type Hemispheric Glioma Harboring Concomitant ALK and EGFR Alteration.

Derya Karatas, Saygi Uygur, Irmak Tekeli Barut, Hamide Sayar, Ahmet Dagtekin, Emel Avci

Abstract readCase Reports
In one paragraph

Article in NMC case report journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Derya KaratasDepartment of Neurosurgery, Faculty of Medicine, Mersin University, Mersin, Türkiye.
Saygi UygurDepartment of Neurosurgery, Faculty of Medicine, Mersin University, Mersin, Türkiye.
Irmak Tekeli BarutDepartment of Neurosurgery, Faculty of Medicine, Mersin University, Mersin, Türkiye.
Hamide SayarDepartment of Pathology, Faculty of Medicine, Mersin University, Mersin, Türkiye.
Ahmet DagtekinDepartment of Neurosurgery, Faculty of Medicine, Mersin University, Mersin, Türkiye.
Emel AvciDepartment of Neurosurgery, Faculty of Medicine, Mersin University, Mersin, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Infant-type hemispheric glioma is a subtype of pediatric high-grade glioma that is seen among those under the age of 3-5 years and congenital infant-type hemispheric gliomas are another subtype which is seen among those under 6 months of age. The molecular features and overall survival of infant-type hemispheric gliomas are distinct from those of pediatric and adult high-grade gliomas. The present study reports a fraternal twin case of a giant hemispheric infant-type hemispheric glioma diagnosed at the age of 2 months and treated with gross total resection. Even though the Ki-67 proliferative index of the tumor was 70%, she has been surviving for 4 years. After molecular analysis, the first case of infant-type hemispheric glioma that had concurrent

Indexed as

anaplastic lymphoma kinasecongenital cancerhigh-grade gliomas

Identifiers

PMID40151500
PMCPMC11947719

What OpenQuestion holds

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Registered trials

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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.