Primary cardiac synovial sarcoma: A case report and literature review
Corresponding Author
Yuki Yokouchi
Departments of Surgical Pathology
Yuki Yokouchi, MD, Department of Surgical Pathology, Toho University Ohashi Medical Center, 2-17-6, Ohashi, Meguro-ku, Tokyo, 153-8515, Japan. Email: [email protected]Search for more papers by this authorNobuyuki Hiruta
Department of Surgical Pathology, Toho University Sakura Medical Center, Chiba
Search for more papers by this authorYoshinao Oda
Department of Anatomic Pathology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan
Search for more papers by this authorTatsuya Gomi
Radiology, Toho University Ohashi Medical Center, Tokyo
Search for more papers by this authorCorresponding Author
Yuki Yokouchi
Departments of Surgical Pathology
Yuki Yokouchi, MD, Department of Surgical Pathology, Toho University Ohashi Medical Center, 2-17-6, Ohashi, Meguro-ku, Tokyo, 153-8515, Japan. Email: [email protected]Search for more papers by this authorNobuyuki Hiruta
Department of Surgical Pathology, Toho University Sakura Medical Center, Chiba
Search for more papers by this authorYoshinao Oda
Department of Anatomic Pathology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan
Search for more papers by this authorTatsuya Gomi
Radiology, Toho University Ohashi Medical Center, Tokyo
Search for more papers by this authorAbstract
Primary cardiac synovial sarcoma is a rare disease. A 51-year-old man visited our hospital with the chief complaint of palpitations and shortness of breath while exercising. Copious bloody pericardial effusion and a multicystic intrapericardial tumor were detected. A primary cardiac malignant tumor was suspected, an open-chest tumor resection was performed with the objectives of diagnosis and treatment. Histologically, the tumor cells were uniformly spindle-shaped with an ovoid or oval nucleus, they had proliferated in fascicular fashion. In addition myxoid degeneration, a hemangiopericytomatous vascular pattern and pseudorosette formation were seen in some areas of the tumor. Based on the histopathological and immunohistochemical findings and reverse transcription polymerase chain reaction detection of SS18-SSX1 fusion transcripts, a monophasic fibrous type synovial sarcoma was diagnosed. Postoperative radiation therapy was administered and there had been no recurrence 9 months after the surgery.
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