Evidence map›Paper›PMID 42742714›Full record

ReviewRadiologie (Heidelberg, Germany)2026

[Spinal tumors in childhood and adolescence].

Alena Haußmann

Abstract readEnglish AbstractReview
PubMed Publisher
In one paragraph

Review in Radiologie (Heidelberg, Germany), 2026. 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

1 author.

Alena HaußmannKlinik für Diagnostische und Interventionelle Neuroradiologie, Universitätsklinikum des Saarlandes, Kirrberger Straße, 66424, Homburg-Saar, Deutschland. alena.haussmann@uks.eu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spinal tumors are a rare tumor entity in children and adolescents, accounting for approximately 4-10% of all central nervous system (CNS) tumors. Based on their anatomical location, they are classified as intradural or extradural and intradural tumors are further subdivided into intramedullary and extramedullary lesions. The clinical symptoms are often nonspecific, with persistent back pain being the most common initial symptom. Neurological manifestations, including sensory and motor deficits, typically develop later in the course of the disease. The imaging modality of choice is magnetic resonance imaging (MRI) of the entire spinal axis and when indicated the head. The various tumor entities exhibit characteristic imaging features that should be recognized as they are essential for accurate diagnosis and appropriate treatment planning.

Indexed as

Atypical teratoid rhabdoid tumourCharacteristic featuresMagnetic resonance imagingPrimitive neuroectodermal tumourVon Hippel–Lindau syndrome

Identifiers

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.