Evidence map›Paper›PMID 38025355›Full record

ArticleJournal of orthopaedic case reports2023

Unusually Giant Solitary Osteochondroma of the Ilium: A Case Report with Review of Literature.

Mohit J Jain, Shubham S Kapadiya, Yash M Mutha, Vatsal J Mehta, Kshemankar K Shah, Aditya K Agrawal

Open access · goldAbstract readCase Reports
In one paragraph

Article in Journal of orthopaedic case reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-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

4 citing papers in PubMed, 2 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

Mohit J JainDepartment of Orthopedics, SBKS Medical Institute and Research Center at Sumandeep Vidyapeeth and Dhiraj Hospital, Waghodia, Vadodara, India.
Shubham S KapadiyaDepartment of Orthopedics, SBKS Medical Institute and Research Center at Sumandeep Vidyapeeth and Dhiraj Hospital, Waghodia, Vadodara, India.
Yash M MuthaDepartment of Orthopedics, SBKS Medical Institute and Research Center at Sumandeep Vidyapeeth and Dhiraj Hospital, Waghodia, Vadodara, India.
Vatsal J MehtaDepartment of Orthopedics, SBKS Medical Institute and Research Center at Sumandeep Vidyapeeth and Dhiraj Hospital, Waghodia, Vadodara, India.
Kshemankar K ShahDepartment of Orthopedics, SBKS Medical Institute and Research Center at Sumandeep Vidyapeeth and Dhiraj Hospital, Waghodia, Vadodara, India.
Aditya K AgrawalDepartment of Orthopedics, SBKS Medical Institute and Research Center at Sumandeep Vidyapeeth and Dhiraj Hospital, Waghodia, Vadodara, India.
Institute of Medical Sciences and Sum Hospital · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Osteochondroma is the most common benign bone tumor where a chondrogenic lesion is derived from aberrant cartilage from the perichondral ring. Although it commonly arises from the growing ends of long bones, less commonly, it may arise from the scapula, pelvis, or vertebra. Case Report: We encountered a 16-year-old male patient with a painless left pelvic solid mass for 3 years, which was suggestive of osteochondroma on X-ray and magnetic resonance imaging findings. Besides cosmetic issues, the main indication for surgery was the constant discomfort in wearing pants/shorts/belts. He underwent en bloc excision followed by a biopsy of the surgical specimen by two independent histopathologists confirming the tumor to be osteochondroma. He was followed up for 2 years with no signs of post-operative complications or recurrence. This case represents one of the very few reported so affecting the iliac wing, where the excision was performed before skeletal maturation. We also performed a review of the current literature on iliac wing osteochondroma to understand the tumor better, identify gaps in current knowledge, and suggest areas for future research. Conclusion: Since one of the differential diagnoses includes secondary chondrosarcoma, which could be a rare progression of osteochondroma, early recognition and comprehensive evaluation of such unusual cases needs to be dealt with a high index of suspicion to avoid misdiagnosis and to provide effective treatment.

Indexed as

En bloc excisioniliumosteochondroma

Identifiers

PMID38025355
PMCPMC10664206
OpenAlexW4388677041

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.