Abstract
Soft tissue sarcomas are rare, accounting for approximately 1% of all malignant tumors (Suit et al. 1975). Most patients present with large, high-grade tumors that are very aggressive locally and tend to spread hematogenously. In general, adults have a worse prognosis than children with the same sarcoma. The largest series of genitourinary sarcomas is from Memorial Sloan-Kettering Cancer Center involving a prospective data base of 43 patients. This study revealed that 86% of tumors were high grade, 56% of tumors were >5 cm in diameter and 21% of the patients presented with metastatic disease (Russo et al. 1992). In this series, complete surgical resection was possible in 58% of cases. The authors reported an actuarial relapse-free survival rate for urologic sarcomas of 55% and 40% at 3 and 5 years, respectively, regardless of histologic type, patient age, or sex (Russo et al. 1992). Despite the modern forms of therapy used in this series, their data are not significantly different from historical controls (Powers et al. 1956).
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Salem, C.E., Stein, J.P., Skinner, D.G. (1999). Adult Genitourinary Sarcomas: Pelvic Sarcomas. In: Petrovich, Z., Baert, L., Brady, L.W. (eds) Carcinoma of the Kidney and Testis, and Rare Urologic Malignancies. Medical Radiology. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-59839-5_33
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DOI: https://doi.org/10.1007/978-3-642-59839-5_33
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