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Updated: Apr 25, 2026

Author Spotlight: Exploring the Role of Inflammation in the Co-occurrence of Primary Sjogren's Syndrome and Lung Adenocarcinoma
Published on: September 20, 2024
Primary synovial sarcoma of lung.
Devleena1, Vikram Bansal1, Tamohan Chaudhuri1
1Department of Radiation Oncology and Pathology, Saroj Gupta Cancer Centre and Research Institute, Mahatma Gandhi Road, Thakurpukur, Kolkata, West Bengal, India.
Synovial sarcoma (SS) is a rare cancer. This report details an extremely rare case of primary pulmonary SS presenting as chest pain and a lung mass, confirmed via biopsy and immunohistochemistry.
Area of Science:
- Oncology
- Pathology
- Radiology
Background:
- Synovial sarcoma (SS) is a rare malignancy typically arising near joints but can occur in diverse tissues.
- Primary pulmonary synovial sarcoma is exceptionally rare, posing diagnostic challenges.
Purpose of the Study:
- To report a rare case of primary pulmonary synovial sarcoma.
- To highlight the diagnostic features and methodology for this rare tumor.
Main Methods:
- Computed tomography (CT) scan of the thorax for initial imaging.
- CT-guided core biopsy for tissue acquisition.
- Immunohistochemistry (IHC) for definitive diagnosis.
Main Results:
- The patient presented with severe chest pain and a large right lung mass with pleural effusion on CT.
- Immunohistochemistry revealed tumor cells expressing EMA, bcl 2, Vimentin, and smooth muscle actin.
- Tumor cells were immunonegative for S100 and cytokeratin, supporting the diagnosis.
Conclusions:
- Primary pulmonary synovial sarcoma is an extremely rare entity.
- CT-guided biopsy and IHC are crucial for diagnosing primary pulmonary SS.
- This case underscores the importance of considering rare diagnoses in pulmonary masses.
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