| Autor: |
Cianciulli TF; División Cardiología, Hospital General de Agudos Dr. Cosme Argerich, Buenos Aires, Argentina. E-mail: tcianciulli@gmail.com.; Ministerio de Salud, Gobierno de la Ciudad Autónoma de Buenos Aires, Buenos Aires, Argentina., Saccheri MC; División Cardiología, Hospital General de Agudos Dr. Cosme Argerich, Buenos Aires, Argentina., Lax JA; División Cardiología, Hospital General de Agudos Dr. Cosme Argerich, Buenos Aires, Argentina., Balletti LR; División Cardiología, Hospital General de Agudos Dr. Cosme Argerich, Buenos Aires, Argentina., Arias RV; División Cardiología, Hospital General de Agudos Dr. Cosme Argerich, Buenos Aires, Argentina., Morita LA; División Patología, Hospital General de Agudos Dr. Cosme Argerich, Buenos Aires, Argentina., Beck MA; División Patología, Hospital General de Agudos Dr. Cosme Argerich, Buenos Aires, Argentina., Zappi A; División Patología, Hospital General de Agudos Dr. Cosme Argerich, Buenos Aires, Argentina., Kazelián LR; División Cardiología, Hospital General de Agudos Dr. Cosme Argerich, Buenos Aires, Argentina. |
| Abstrakt: |
Primary pericardial synovial sarcoma is an extraordinarily very rare tumor with a poor prognosis, and little is known about its therapeutic management. We describe the case of a 51-year-old woman patient who underwent incomplete surgical resection, chemotherapy, and radiotherapy. To the best of our knowledge, no primary pericardial synovial sarcoma has been described which, after surgery, remains asymptomatic for 5 years, and until a control CT scan detects cardiac metastases that compromised the lumen of the right cavities and with chemotherapy, echocardiography demonstrated complete resolution of cardiac metastases. |
