Abstract
2/2020
vol. 71
Case report
Synovial sarcoma of the stomach: case report and systematic review of the literature
- Department of Tumor Pathology, Maria Sklodowska-Curie National Research Institute of Oncology, Krakow Branch, Poland
- Department of Pathology Institute of Medical Sciences, Medical College of Rzeszow University, Rzeszow, Poland
- Department of Surgical Oncology, Specialist Hospital, Podkarpacki Oncology Center in Brzozow, Poland
- Department of Radiology and Imaging Sciences, Specialist Hospital, Podkarpacki Oncology Center in Brzozow, Poland
Pol J Pathol 2020; 71 (2): 181-193
Online publish date: 2020/07/22
Synovial sarcoma is a rare mesenchymal malignant neoplasm that presents a specific t(X;18) translocation forming SS18(SYT)-SSX chimera gene. It is most commonly seen in soft tissues of the extremities. The digestive tract is an exceptional site of involvement. We report a case of primary gastric synovial sarcoma in a 48-year-old female. Differential diagnosis of synovial sarcoma from other spindle cell, mesenchymal and cytokeratin-positive tumors is critical for the treatment and prognosis. Immunohistochemistry studies and molecular analysis are required to settle a proper diagnosis.
Keywords
synovial sarcoma, stomach, spindle cell neoplasm, cytokeratin
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