Evidence map›Paper›PMID 37941973›Full record

ArticleInternational medical case reports journal2023

Cerebellar Hemangioblastoma with Leptomeningeal Spread and a Fatal Outcome: A Rare Case Report with

Luis Miguel Chinchilla-Tábora, Javier Ortiz Rodríguez-Parets, Álvaro Otero-Rodríguez, Laura Ruiz Martín, Juan Carlos Paniagua Escudero, Luis Miguel Navarro Martín, Belén Cigarral García, Adelaida Nieto Palacios, Idalia González Morais, José María Sayagués and 1 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in International medical case reports journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 30% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Leptomeningeal hemangioblastoma: illustrative case.Journal of neurosurgery. Case lessons · 2025
    Article
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

11 authors.

Luis Miguel Chinchilla-TáboraDepartment of Pathology, University Hospital of Salamanca and Institute for Biomedical Research of Salamanca, Salamanca, Spain.ORCID 0000-0002-7435-3509
Javier Ortiz Rodríguez-ParetsDepartment of Pathology, University Hospital of Salamanca and Institute for Biomedical Research of Salamanca, Salamanca, Spain.
Álvaro Otero-RodríguezDepartment of Neurosurgery, University Hospital of Salamanca and Institute for Biomedical Research of Salamanca, Salamanca, Spain.ORCID 0000-0001-9421-7830
Laura Ruiz MartínDepartment of Neurosurgery, University Hospital of Salamanca and Institute for Biomedical Research of Salamanca, Salamanca, Spain.
Juan Carlos Paniagua EscuderoDepartment of Radiology, University Hospital of Salamanca and Institute for Biomedical Research of Salamanca, Salamanca, Spain.
Luis Miguel Navarro MartínDepartment of Clinical Oncology, University Hospital of Salamanca and Institute for Biomedical Research of Salamanca, Salamanca, Spain.
Belén Cigarral GarcíaDepartment of Clinical Oncology, University Hospital of Salamanca and Institute for Biomedical Research of Salamanca, Salamanca, Spain.ORCID 0000-0002-5366-704X
Adelaida Nieto PalaciosDepartment of Radiation Oncology, University Hospital of Salamanca and Institute for Biomedical Research of Salamanca, Salamanca, Spain.
Idalia González MoraisDepartment of Pathology, University Hospital of Salamanca and Institute for Biomedical Research of Salamanca, Salamanca, Spain.ORCID 0000-0002-4372-4725
José María SayaguésDepartment of Pathology, University Hospital of Salamanca and Institute for Biomedical Research of Salamanca, Salamanca, Spain.ORCID 0000-0003-0582-3500
María Dolores Ludeña de la CruzDepartment of Pathology, University Hospital of Salamanca and Institute for Biomedical Research of Salamanca, Salamanca, Spain.ORCID 0000-0003-3991-5956

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hemangioblastoma (HB) is a Central Nervous System (CNS) tumor with a generally favorable behavior and prognosis, classified as WHO grade 1. Sporadic HB is not related to any inherited disease, and it usually appears in a single location. Sporadic or VHL-related HBs show variable patterns of growth velocity. Cases of growing HB can cause mild symptoms such as headache, but some cases develop serious complications such as accumulation of cerebrospinal fluid in the brain with secondary neurological damage sometimes being irreversible when early treatment is not started. Our case showed some clinical characteristics more frequently observed in VHL-related HB rather than sporadic HB, and the presence of alterations in

Indexed as

epidermal growth factor receptorfluorescence in situ hybridizationhaemangioblastomahydrocephalusimmunohistochemistrymouse double minute 2

Identifiers

PMID37941973
PMCPMC10629408
OpenAlexW4388298643

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.