Evidence map›Paper›PMID 36414866›Full record

ReviewChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2023

A 13-year patient journey of infant giant clival chordoma: case report and literature review.

J Apps, R Gagen, E Neumann, G Solanki, M English

Open access · hybridAbstract readReviewCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Review in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2023. 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
0.3field-weighted citation impact, top 38% of its field
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, 2 citations in OpenAlex.

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

5 authors at 2 institutions in 1 country.

J AppsDepartment of Oncology, Birmingham Women's and Children's NHS Foundation Trust, Birmingham, UK.
R GagenDepartment of Neurosurgery, Birmingham Women's and Children's NHS Foundation Trust, Birmingham, UK.
E NeumannDepartment of Oncology, Birmingham Women's and Children's NHS Foundation Trust, Birmingham, UK.
G SolankiCancer Research Clinical Trials Unit, University of Birmingham, Birmingham, UK.
M EnglishDepartment of Oncology, Birmingham Women's and Children's NHS Foundation Trust, Birmingham, UK. martinenglish@nhs.net.ORCID 0000-0002-6087-3490
Birmingham Women’s and Children’s NHS Foundation Trust · GBCancer Research UK Clinical Trials Unit · GB

Funding

Cancer Research UK 28028Cancer Research UK 28160
6 · The paper itself

Abstract

Chordomas are rare malignant bone tumours that develop from the ectopic remnants of the embryonic notochord. In contrast to adults, the majority in children under 16 present intra-cranially (63%). In 2006, we reported the youngest case of a large clival chordoma, a 15-week old baby, the second case to present without skull base involvement and the fourth case of chordoma in a patient with tuberous sclerosis (TS) Kombogiorgas (Childs Nerv Syst 22(10):1369-1374, 2006). In this report, we provide an update on this patient's journey through a range of therapeutic options and summarize an update of the literature, since 2006, for this patient group.

Indexed as

ChordomaSkull Base NeoplasmsAdultChildCranial Fossa, PosteriorFacial BonesHumansInfantNeoplasm Recurrence, LocalImatinibInfant clival chordomamTOR

Identifiers

PMID36414866
PMCPMC10159969
OpenAlexW4309651049

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.