Evidence map›Paper›PMID 40927430›Full record

ArticleCase reports in pathology2025

Synovial Sarcoma: Malignant Soft Tissue Sarcoma With Benign Clinical Characteristics-A Case Report.

Jay Lodhia, David Msuya, Joshua Tadayo, Alex Mremi

Abstract readCase Reports
In one paragraph

Article in Case reports in pathology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

1 citing paper in PubMed.

  1. 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

4 authors.

Jay LodhiaDepartment of General Surgery, Kilimanjaro Christian Medical Centre, Moshi, Tanzania.ORCID https://orcid.org/0000-0002-3373-5762
David MsuyaDepartment of General Surgery, Kilimanjaro Christian Medical Centre, Moshi, Tanzania.ORCID https://orcid.org/0000-0003-1653-3365
Joshua TadayoDepartment of General Surgery, Kilimanjaro Christian Medical Centre, Moshi, Tanzania.
Alex MremiFaculty of Medicine, KCMC University, Moshi, Tanzania.ORCID https://orcid.org/0000-0001-7226-0168

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Synovial sarcomas are rare malignant soft tissue tumors with significant metastatic potential. Although they can occur in various parts of the body, they are most commonly found on the extremities. These tumors typically develop in children and young adults, making occurrences in individuals over 50 years of age unusual. Due to their slow-growing and nonpainful nature, synovial sarcomas can often be mistaken for benign pathologies. The standard treatment involves complete surgical excision with negative margins, which offers a favorable 5-year prognosis. This case highlights the importance of early recognition and intervention in managing soft tissue sarcomas. In this case report, we present a 57-year-old African male with a 2-year history of gradual, nonpainful swelling on his left hand, diagnosed as synovial sarcoma. The patient was successfully treated with complete surgical excision.

Indexed as

case reporthandsoft tissue neoplasmsynovial sarcomaTanzania

Identifiers

PMID40927430
PMCPMC12417059

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Registered trials

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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.