Evidence map›Paper›PMID 37901278›Full record

ArticleJournal of neurological surgery reports2023

A Primary Intraosseous Meningioma: A Rare Case of Malignancy with High Proliferative Ability.

Yoshiki Sato, Koichi Mitsuya, Yuko Kakuda, Takuma Oishi, Shoichi Deguchi, Takashi Sugino, Yasuto Akiyama, Takeshi Nagashima, Kenichi Urakami, Yuji Shimoda and 3 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in Journal of neurological surgery reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 41% 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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Primary intraosseous meningioma in a child: an unusual case report and literature review.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2026
    Review
  2. 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

13 authors at 1 institution in 1 country.

Yoshiki SatoDivision of Neurosurgery, Shizuoka Cancer Center, Nagaizumi, Shizuoka, Japan.
Koichi MitsuyaDivision of Neurosurgery, Shizuoka Cancer Center, Nagaizumi, Shizuoka, Japan.ORCID 0000-0001-8956-5427
Yuko KakudaDivision of Diagnostic Pathology, Shizuoka Cancer Center, Nagaizumi, Shizuoka, Japan.
Takuma OishiDivision of Diagnostic Pathology, Shizuoka Cancer Center, Nagaizumi, Shizuoka, Japan.
Shoichi DeguchiDivision of Neurosurgery, Shizuoka Cancer Center, Nagaizumi, Shizuoka, Japan.
Takashi SuginoDivision of Diagnostic Pathology, Shizuoka Cancer Center, Nagaizumi, Shizuoka, Japan.ORCID 0000-0002-0205-0525
Yasuto AkiyamaDivision of Immunotherapy, Shizuoka Cancer Center Research Institute, Nagaizumi, Shizuoka, Japan.
Takeshi NagashimaCancer Diagnostics Research Division, Shizuoka Cancer Center Research Institute, Nagaizumi, Shizuoka, Japan.
Kenichi UrakamiMedical Genetics Division, Shizuoka Cancer Center Research Institute, Nagaizumi, Shizuoka, Japan.
Yuji ShimodaDivision of Immunotherapy, Shizuoka Cancer Center Research Institute, Nagaizumi, Shizuoka, Japan.
Keiichi OhshimaDivision of Medical Genetics Division, Shizuoka Cancer Center Research Institute, Nagaizumi, Shizuoka, Japan.
Nakamasa HayashiDivision of Neurosurgery, Shizuoka Cancer Center, Nagaizumi, Shizuoka, Japan.
Ken YamaguchiShizuoka Cancer Center, Nagaizumi, Shizuoka, Japan.
Shizuoka Cancer Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary intraosseous meningioma (PIM) is a rare tumor that arises in the skull. Histopathologically, it is generally described as a slow-growing, benign lesion. However, on rare occasions, PIM presents as a malignancy with high proliferative ability, which requires maximal resection, adjuvant radiotherapy, and subsequent careful follow-up. Because of the rarity of such cases, they present a diagnostic challenge with unusual pathological findings. Herein, we report a case of a primary intraosseous anaplastic meningioma with extensive invasion inside and outside the skull, along with the results of whole-genome analysis. Histopathological diagnosis was a World Health Organization grade 3 anaplastic meningioma. In the literature, only two cases of anaplastic PIM have been reported, so its characteristics and treatment are poorly understood. Our patient was successfully treated with tumor resection, followed by intensity-modulated radiation therapy. Follow-up imaging studies revealed no recurrence or distant metastasis, including to lung, liver, and bone, at 8 months after the surgery.

Indexed as

anaplasticextensive invasiongenetic analysisintraosseousmeningioma

Identifiers

PMID37901278
PMCPMC10611535
OpenAlexW4386243546

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.