ArticleCase reports in pathology2020
Primary Intraosseous Synovial Sarcoma with Molecular Confirmation: Expanding and Clarifying the Spectrum of This Rare Neoplasm.
Article in Case reports in pathology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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.
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Who cites it
8 citing papers in PubMed, 11 citations in OpenAlex.
- Primary Intraosseous Synovial Sarcoma: Experience from a Tertiary Cancer Center.South Asian journal of cancer · 2025Article
- Synovial sarcoma: A case report of first presentation at penoscrotal junction.Urology case reports · 2025Article
- Primary pleuropulmonary synovial sarcoma presenting with recurrent spontaneous pneumothorax.BMJ case reports · 2023Article
- A Rare Case of Humerus Synovial Sarcoma Originated from Bone Tissue: Case Report.Advanced biomedical research · 2023Article
- Malignant primary intraosseus synovial sarcoma - a rare case report.Radiology case reports · 2022Article
- Commentary: Case report: Primary intraosseous poorly differentiated synovial sarcoma of the femur.Frontiers in oncology · 2022Article
- Case Report: Primary Intraosseous Poorly Differentiated Synovial Sarcoma of the Femur.Frontiers in oncology · 2022Article
- The rare primary bone sarcomas: imaging-pathological correlation.Skeletal radiology · 2021Review
Corrections and comments
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Authors and funding
4 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Synovial sarcoma is a well-known malignant tumor usually originating within deep soft tissues of the lower extremities of adolescents and young adults. Rare radiologically confirmed examples of primary bone synovial sarcoma have been documented, generally in isolated case reports. Herein, we report two cases of primary intraosseous synovial sarcoma, with molecular confirmation, involving the left humerus of a 45-year-old female and the right fourth metatarsal bone in a 36-year-old male. Additionally, we clarify the spectrum of primary intraosseous synovial sarcoma by separately analyzing reported cases with radiographic confirmation of bone origin and molecular support for the diagnosis. There are clinicopathologic differences between those tumors with documented molecular confirmation and those lacking such confirmation, specifically regarding their anatomic distribution (
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Registered trials
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.