Evidence map›Paper›PMID 40129829›Full record

ArticleRadiology case reports2025

A rare case of chondroblastoma of the jugular foramen: Imaging and pathological features.

Kai-Jie Wang, Tian-Cheng Lin, Wei-Yuan Huang

Abstract readCase Reports
In one paragraph

Article in Radiology case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

3 authors.

Kai-Jie WangDepartment of Radiology, Hainan Affiliated Hospital of Hainan Medical University (Hainan General Hospital), NO. 19, Xiuhua St, Xiuying Dic, Haikou, Hainan, 570311, PR China.
Tian-Cheng LinDepartment of Radiology, Hainan Affiliated Hospital of Hainan Medical University (Hainan General Hospital), NO. 19, Xiuhua St, Xiuying Dic, Haikou, Hainan, 570311, PR China.
Wei-Yuan HuangDepartment of Radiology, Hainan Affiliated Hospital of Hainan Medical University (Hainan General Hospital), NO. 19, Xiuhua St, Xiuying Dic, Haikou, Hainan, 570311, PR China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chondroblastoma is a rare benign tumor that typically arises in the epiphyses or apophyses of long bones in patients with immature skeletal structures. Occasionally, it presents in atypical sites such as the bones of the foot and craniofacial region. This report details the case of an 18-year-old female who experienced neck pain and was found to have a lesion in the left jugular foramen. Imaging revealed typical lytic and expansive bone destruction with invasion into the adjacent internal jugular vein. Initially misdiagnosed as a glomus jugulare tumor, definitive diagnosis of chondroblastoma was established postoperatively via histopathology. This case underscores the diagnostic challenges posed by chondroblastomas at atypical sites. Through detailed imaging, histopathological analysis, and literature review, this study aims to enhance the awareness of clinicians and radiologists regarding chondroblastoma and provides insights and references for the diagnosis and management of similar cases in the future.

Indexed as

ChondroblastomaGlomus jugulare tumorJugular foramenMagnetic resonance imaging

Identifiers

PMID40129829
PMCPMC11930521

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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.