Evidence map›Paper›PMID 39968065›Full record

ArticleFrontiers in oncology2025

Case report: Primary intraosseous meningioma: a radiological study of two cases confirmed pathologically.

Yue Wang, Jibo Hu

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Article in Frontiers in oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Yue WangDepartment of Radiology, The Fourth Affiliated Hospital of School of Medicine, and International School of Medicine, International Institutes of Medicine, Zhejiang University, Yiwu, China.
Jibo HuDepartment of Radiology, The Fourth Affiliated Hospital of School of Medicine, and International School of Medicine, International Institutes of Medicine, Zhejiang University, Yiwu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Primary intraosseous meningioma (PIM) is a rare lesion often misidentified preoperatively due to its ambiguous benign or malignant characteristics. In this report, we introduce two novel cases of PIM and explore the potential correlation between pathological classification and imaging features. Our aim is to enhance our understanding of PIM and improve its preoperative diagnosis. Case presentation: The first case is a 68-year-old female patient presenting with a brain mass located in the temporal region. Computed tomography (CT) imaging demonstrated the destruction of adjacent bone structures. A right frontal temporal craniectomy was subsequently performed and histological examination pathologically confirmed the lesion was the chordoid variant of PIM. The second case is a 56-year-old male patient who exhibited an irregular soft-tissue mass in the right sphenoid as visualized on brain CT. The patient underwent a surgical intervention for a skull base neoplasm. Postoperative pathological analysis confirmed the presence of the meningothelial variant of PIM. Upon pathological examination, the two cases were respectively classified as atypical meningioma (Grade II) and benign meningioma (Grade I). Conclusions: While pathological examination remains indispensable for the definitive confirmation of PIM, the early identification of PIM is critically dependent on radiological imaging methods. The imaging characteristics of PIM exhibit variability across different pathological grades, a factor that can significantly aid in both the diagnostic process and the formulation of appropriate treatment strategies.

Indexed as

case reportdiagnosisintraosseousmeningiomapathology

Identifiers

PMID39968065
PMCPMC11832408

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