ArticleIndian journal of surgical oncology2018
A Case of Primary Intra-abdominal Synovial Sarcoma.
Article in Indian journal of surgical oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed, 10 citations in OpenAlex.
- A rare case report of omental synovial sarcoma complicated hemoperitoneum and literature review.World journal of surgical oncology · 2024Review
- Incidental intra-abdominal synovial sarcoma.BMJ case reports · 2023Article
- A case of primary mesenteric synovial sarcoma: a challenging presentation.Surgical case reports · 2023Article
- SS18-SSX Translocation FISH Negative Mesenteric Synovial Sarcoma-Documentation of an Extremely Rare Entity.Journal of gastrointestinal cancer · 2021Article
- A 64-year-old woman with primary synovial sarcoma of the abdominal wall.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologieArticle
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 sarcomas are relatively common intermediate-to-high-grade malignant soft tissue tumors, often with an initial indolent course. And among the sarcomas primary intra-abdominal synovial sarcoma is a relatively rare entity that may present with an abdominal mass and diagnosis is usually confirmed by immunohistochemistry. The authors report a case of a 46-year-old man who presented with a large palpable abdominal mass. Contrast-enhanced computed tomography (CT) scan showed a large well-defined heterogeneous intra-abdominal mass filling the entire pelvis and extending upwards till the subhepatic region causing displacement of intra-abdominal organs. However, no other focal lesions were seen in the solid organs. The same findings were confirmed on surgery. Histopathology was suggestive of desmoid tumor/hemangiopericytoma. Immunohistochemistry showed positive markers corresponding to synovial sarcoma. The patient was advised to undergo chemotherapy which was refused and follow-up was lost. After 10 months, patient presented for follow-up CT, which showed marked increase in size of the lesion.
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