Raut Chandrajit P, Pisters Peter W T
Department of Surgery, Brigham and Women's Hospital and Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
J Surg Oncol. 2006 Jul 1;94(1):81-7. doi: 10.1002/jso.20543.
Retroperitoneal sarcomas (RPS) are rare tumors, accounting for approximately 15% of soft tissue sarcomas. Surgical resection of localized tumors with gross and microscopically negative margins remains the standard of care. However, because RPS are frequently large and locally advanced, resections are often incomplete, resulting in local recurrence. Investigators are evaluating combined-modality therapies to improve local control and disease-specific survival. This review outlines current concepts and evolving treatment strategies in the diagnosis, staging, and management of RPS.
腹膜后肉瘤(RPS)是罕见肿瘤,约占软组织肉瘤的15%。对局限性肿瘤进行手术切除,切缘在大体和显微镜下均为阴性,仍是标准的治疗方法。然而,由于RPS通常体积较大且局部进展,手术切除往往不完整,导致局部复发。研究人员正在评估联合治疗方案,以改善局部控制和疾病特异性生存率。本综述概述了RPS诊断、分期和管理方面的当前概念及不断发展的治疗策略。