The Journal of the Japanese Society of Clinical Cytology
Online ISSN : 1882-7233
Print ISSN : 0387-1193
ISSN-L : 0387-1193
Clinical Articles
Primary synovial sarcoma of the lung—Case of report—
Yosuke HIRABAYASHI, Meiko OGAWA, Hisako HASHIMOTO, Mieko FUJIWARA, Koyu SUZUKI, Mizuto OTSUJI, Tatsuo SAWADA, Hiroshi HASHIMOTO
Author information
JOURNAL FREE ACCESS

2008 Volume 47 Issue 2 Pages 122-126

Details
Abstract
Background : Most synovial sarcomas arise around joints, and primary synovial sarcoma of the lung is rare. We report a case of primary synovial sarcoma of the right lung.
Case : A 48-year-old man was admitted to our hospital because of an abnormal shadow in the right middle lung field detected during a medical checkup. A CT examination revealed a round mass in the hilum of the right lung. Right upper and middle lobectomy was performed, and touch smear cytology of the tumor showed fascicles of spindle-shaped to round tumor cells containing bland, uniform nuclei, and finely light-green-staining cytoplasm. Histologically, the tumor was composed of densely proliferating uniform spindle-shaped to oval cells in fascicles. The tumor cells were immunohistochemically positive for vimentin, CD99, bcl-2, cytokeratin AE1/AE3, and EMA. RT-PCR performed on paraffin-embedded sections demonstrated fusion gene transcripts of SYT-SSX1. A diagnosis of synovial sarcoma of the lung, monophasic fibrous type, was made.
Conclusion : Synovial sarcoma of the lung is rare. Diagnosis of spindle-cell tumors by cytological examination alone is difficult. To achieve a definitive diagnosis, it is important to include synovial sarcoma in the differential diagnosis during the cytodiagnostic procedure, and immunohistochemistry, cytogenetic, and molecular studies are necessary.
Content from these authors
© 2008 The Japanese Society of Clinical Cytology
Previous article Next article
feedback
Top