Key result
Cytology and immunohistochemistry successfully diagnose primary pulmonary synovial sarcoma in a lung mass.
Case Report (n=1)
Cytologic analysis combined with immunohistochemistry can successfully diagnose rare primary pulmonary synovial sarcoma.
Supports cytologic diagnosis of rare pulmonary synovial sarcoma; hypothesis-generating and requires validation in larger series.
Synovial sarcoma is a common soft tissue sarcoma with variable fibrous and epithelial differentiation that rarely arises from other body sites, such as within the lung. A case of a 68-year-old male with an extensive smoking history who presented with chest pain and a primary, central, metabolically active lung mass was reported. The mass was biopsied by bronchial brushing, bronchoalveolar lavage (BAL), and transbronchial fine-needle aspiration (FNA). Cytologic analysis of bronchial brushing, BAL, and FNA revealed single and clusters of atypical spindle cells, oval, or spindle-shaped nuclei with smooth nuclear membranes, hyperchromatic and granular chromatin, scant to moderate and delicate cytoplasm, a high degree of mitotic figures, and a lack of necrosis. Immunohistochemical studies showed that the tumor cells were positive for CD99, BCL2, and CK7. A diagnosis of synovial sarcoma was rendered. The differential diagnosis of primary pulmonary synovial sarcoma is discussed, including neuroendocrine tumors, squamous cell carcinoma, and various sarcomatous tumors.
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Pyden et al. (2016) conducted a case report in Synovial sarcoma (n=1). Cytologic analysis and immunohistochemical studies was evaluated on Diagnosis of synovial sarcoma. Cytologic analysis and immunohistochemical studies successfully diagnosed a primary pulmonary synovial sarcoma in a 68-year-old male presenting with a lung mass.
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