Key result
Rare primary pulmonary synovial sarcoma case highlights the need for core biopsy and immunohistochemistry.
Why the study?
Primary pulmonary synovial sarcoma is a very rare and highly aggressive tumor that is often difficult to diagnose due to nonspecific clinical and radiological presentations and the limitations of FNAC.
Case Report (n=1)
Highlights the diagnostic challenge of primary pulmonary synovial sarcoma and the preference for core biopsy over FNAC for accurate diagnosis.
Supports core biopsy plus immunohistochemistry for suspected primary pulmonary synovial sarcoma; leaves open generalizability from single case.
Primary pulmonary synovial sarcoma is a very rare, but highly aggressive tumor. Metastatic pulmonary sarcoma due to hematogenous dissemination is much more common. Hence why in any case of pulmonary sarcoma, whole body survey is necessary to exclude a primary tumor elsewhere. No clinical or radiological presentations are specific for pulmonary sarcoma hence; it is often confused with bronchogenic carcinoma. On the other hand, image-guided fine needle aspiration cytology (FNAC) is very much helpful in diagnosis of bronchogenic carcinoma, whereas, it may be inclusive in cases pulmonary sarcomas including primary synovial sarcoma, especially in cases of huge pulmonary masses. So why image-guided tru-cut core biopsy or open lung biopsy and their histopathological examination, supplemented by immunohistochemistry are preferable for the tissue diagnosis of pulmonary synovial sarcoma, although FNAC and immunocytochemistry may be used for the diagnosis. Surgical resection is treatment of choice, if it is not possible, palliative chemotherapy may be an option. Here, we report a rare case of primary synovial sarcoma which occupied almost whole of the right hemithorax in a 60-year-old male farmer.
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Das et al. (2016) conducted a case report in Primary pulmonary synovial sarcoma (n=1). A rare case of primary pulmonary synovial sarcoma occupying almost the whole right hemithorax was reported in a 60-year-old male, highlighting the need for core biopsy and immunohistochemistry for diagnosis.
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