Conclusions
Retroperitoneal sarcomas comprise a rare, heterogeneous group of neoplasms. Routine workup should include the medical history, a physical examination, and helical CT of the abdomen and pelvis with selective use of MRI and preoperative tissue sampling. The primary treatment is complete surgical resection with a rim of normal tissue. The role of adjuvant therapy is evolving and at present should not be used outside the investigational setting.
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Porter, G.A., Feig, B.W. (2003). Retroperitoneal Sarcomas. In: Saclarides, T.J., Millikan, K.W., Godellas, C.V. (eds) Surgical Oncology. Springer, New York, NY. https://doi.org/10.1007/0-387-21701-0_42
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DOI: https://doi.org/10.1007/0-387-21701-0_42
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