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DOI: 10.1148/rg.263055211
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RadioGraphics 2006;26:923-940


AFIP ARCHIVES

From the Archives of the AFIP

Pleuropulmonary Synovial Sarcoma1

Aletta Ann Frazier, MD, Teri J. Franks, MD, Robert D. Pugatch, MD and Jeffrey R. Galvin, MD

1 From the Departments of Radiologic Pathology (A.A.F., J.R.G.) and Pulmonary and Mediastinal Pathology (T.J.F.), Armed Forces Institute of Pathology, 14th St and Alaska Ave NW, Washington, DC 20306-6000; and the Department of Diagnostic Radiology, University of Maryland School of Medicine, Baltimore, Md (A.A.F., R.D.P., J.R.G.). Received December 15, 2005; revision requested January 18, 2006 and received February 15; accepted February 20. All authors have no financial relationships to disclose. Address correspondence to A.A.F. (e-mail: frazier{at}afip.osd.mil).

Pleuropulmonary synovial sarcoma (PPSS) is increasingly recognized as a subtype of sarcoma because of the recent identification of a distinctive chromosomal translocation specific to synovial sarcoma. Soft-tissue synovial sarcoma is far more common than PPSS and typically develops in para-articular locations of the extremities; affects young and middle-aged adults, with no difference in distribution between the sexes; and has well-documented radiologic manifestations. PPSS may arise in the chest wall, heart, mediastinum, pleura, or lung, and it shares patient demographics and several imaging features with its soft-tissue counterpart. Patients present with a cough, chest pain, or dyspnea. On chest radiographs, PPSS typically appears as a sharply marginated mass with uniform opacity, based either in the pleura or in the lung, and often accompanied by an ipsilateral pleural effusion. Computed tomographic images show a well-circumscribed heterogeneously enhanced lesion without associated involvement of bone and without calcifications (except in the case of a chest wall primary tumor). Magnetic resonance imaging provides superior demonstration of nodular soft tissue and multilocular fluid-filled internal components of PPSS, in addition to peripheral rim enhancement after the intravenous administration of a gadolinium-based contrast material such as gadopentetate dimeglumine. Current treatment consists of surgical resection followed by chemotherapy, radiation therapy, or both.




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