Gastric synovial sarcoma (GSS) is an exceptionally rare mesenchymal malignancy, with only 51 cases reported. We present a case of a man in his 50s with dyspeptic symptoms and epigastric pain. Gastroscopy revealed an ulcerous tumour below the gastro-oesophageal junction. Histology, immunohistochemistry and molecular analysis confirmed SS18::SSX1 fusion, diagnostic of synovial sarcoma. The patient underwent successful robot-assisted partial gastric resection with negative margins. No recurrence was noted at 6-month follow-up. This case underscores the diagnostic challenge of GSS, the critical role of molecular techniques and the efficacy of minimally invasive surgical management.
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Thabeya Elango
Johan Tolstrup
Luit Penninga
BMJ Case Reports
Rigshospitalet
Aalborg University
Aalborg University Hospital
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Elango et al. (Wed,) studied this question.
www.synapsesocial.com/papers/69d894526c1944d70ce054c2 — DOI: https://doi.org/10.1136/bcr-2025-267170
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