Evidence map›Paper›PMID 42321738›Full record

ArticleBMC musculoskeletal disorders2026

Subcutaneous extraskeletal osteosarcoma of the gluteal region: a case report from a resource-limited setting.

Yan Feng, Aleki Fuimaono, Sione Pifeleti, Seventeen Toumoua, Tieying Zhang, Yan Liang, Xu Ding

Abstract readCase Reports
In one paragraph

Article in BMC musculoskeletal disorders, 2026. 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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1 · What the graph read from it

What it found

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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

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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.

Yan FengDepartment of Radiology, Jilin Province People's Hospital, Changchun, China.
Aleki FuimaonoDepartment of Surgery, Tupua Tamasese Meaole Hospital, Apia, Samoa.
Sione PifeletiDepartment of Surgery, Tupua Tamasese Meaole Hospital, Apia, Samoa.
Seventeen ToumouaDepartment of Pathology, Tupua Tamasese Meaole Hospital, Apia, Samoa.
Tieying ZhangDepartment of Oncology, Jilin Province People's Hospital, Changchun, Jilin, China.
Yan LiangDepartment of Radiology, Jilin Province People's Hospital, Changchun, China.
Xu DingDepartment of Oncology, Jilin Province People's Hospital, Changchun, Jilin, China. dingxu198@163.com.ORCID https://orcid.org/0000-0002-5915-0009

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundExtraskeletal osteosarcoma (ESOS) is a rare high-grade malignant mesenchymal tumor that produces osteoid in soft tissue without skeletal involvement. Subcutaneous ESOS is exceptionally uncommon and may mimic benign soft tissue lesions. CASE PRESENTATION: A 45-year-old Samoan man presented with a one-year history of a progressively enlarging, painless left gluteal mass. Contrast-enhanced CT showed a well-circumscribed subcutaneous lesion measuring 9.1 × 10.4 × 8.6 cm, with mild to moderate delayed enhancement and no osseous involvement. The tumor was surgically excised. Histopathology showed a spindle to pleomorphic high-grade sarcoma with osteoid produced by atypical tumor cells. Immunohistochemistry showed SATB2 positivity and negative staining for S100, SOX10, pan-cytokeratin, and ERG. The tumor involved the deep resection margin, consistent with R1 resection; the closest margin distance was not specified. The patient declined adjuvant therapy and was subsequently lost to follow-up.

conclusionsSubcutaneous ESOS is rare and diagnostically challenging. This case highlights the importance of imaging, histopathology, immunohistochemistry, and multidisciplinary management, particularly in resource-limited settings.

Indexed as

OsteosarcomaSoft Tissue NeoplasmsButtocksHumansMaleMiddle AgedTomography, X-Ray ComputedCase reportExtraskeletal osteosarcomaSATB2Soft tissue sarcomaSubcutaneous tumor

Identifiers

PMID42321738
PMCPMC13531768

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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.