Evidence map›Paper›PMID 33082304›Full record

ArticleThe American journal of case reports2020

Atypical Imaging of Hemorrhagic Lumbosacral Myxopapillary Ependymoma with Histopathological Correlation: A Case Report.

Fahad Albadr, Salha M Albahkali, Mohammad S Alahmadi, Hussein M Alsakkaf, Amro Al-Habib, Hisham Alkhalidi, Ali A Basalamah

Open access · hybridAbstract readCase Reports
In one paragraph

Article in The American journal of case reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact, top 88% 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

5 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Article
  3. Anomalous hemorrhage in myxopapillar ependymoma: illustrative case.Journal of neurosurgery. Case lessons · 2026
    Article
  4. Article
  5. 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

7 authors at 2 institutions in 1 country.

Fahad AlbadrRadiology Unit, King Saud University Medical City (KSUMC), College of Medicine, King Saud University, Riyadh, Saudi Arabia.
Salha M AlbahkaliDepartment of Radiology, King Fahad Medical City (KFMC), Riyadh, Saudi Arabia.
Mohammad S AlahmadiDepartment of Radiology, King Fahad Medical City (KFMC), Riyadh, Saudi Arabia.
Hussein M AlsakkafRadiology Unit, King Saud University Medical City (KSUMC), College of Medicine, King Saud University, Riyadh, Saudi Arabia.
Amro Al-HabibMedical Imaging Administration, King Fahad Medical Medical City (KFMC), Riyadh, Saudi Arabia.
Hisham AlkhalidiPathology Department, King Saud University, College of Medicine, Riyadh, Saudi Arabia.
Ali A BasalamahNeurosurgery Division, Surgery Department, King Saud University Medical City (KSUMC), College of Medicine, King Saud University, Riyadh, Saudi Arabia.
King Fahd Medical City · SAKing Saud University · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Spinal myxopapillary ependymoma (MPE) is a slow-growing tumor arising from ependymal cells of the central nervous system. MPE rarely presents with acute neurological compromise and most commonly occur in the filum terminale or conus medullaris region. To date, only a few cases have been reported of patients presenting acutely because of hemorrhagic MPE. CASE REPORT A 16-year-old boy without previous medical problems presented with a sudden onset of severe pain in the low back radiating to the thighs. He could not walk owing to the severity of the pain. Neurological examination revealed an unsteady gait, but the rest of the motor and sensory examination was normal. Lumbosacral spine magnetic resonance imaging revealed an intradural hemorrhagic mass extending from L5 to S2. The encapsulated hemorrhagic tumor was resected, and the pathology was consistent with MPE grade I. The patient made a significant recovery postoperatively. It is extremely rare for MPE to present with spontaneous hemorrhage in the lumbosacral region. Prompt diagnosis and management led to a favorable outcome. This case report is intended to highlight the atypical presentation and imaging features of hemorrhagic MPE. CONCLUSIONS We described a rare case of MPE in the lumbosacral region of a patient who presented with acute neurological compromise and atypical imaging features.

Indexed as

Cauda EquinaEpendymomaSpinal Cord NeoplasmsAdolescentHemorrhageHumansMagnetic Resonance ImagingMale

Identifiers

PMID33082304
PMCPMC7588349
OpenAlexW3086507679

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.