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[腹膜后软组织肉瘤的外科治疗——综述]

[Surgical management of retroperitoneal soft-tissue sarcomas--an overview].

作者信息

Garlipp B, Schulz H-U, Zeile M, Lippert H, Meyer F

机构信息

Universitätsklinikum Magdeburg, Klinik für Allgemein-, Viszeral- und Gefäßchirurgie, Magdeburg, Deutschland.

出版信息

Zentralbl Chir. 2010 Dec;135(6):564-74. doi: 10.1055/s-0030-1247414. Epub 2010 Jul 19.

Abstract

INTRODUCTION

Retroperitoneal soft-tissue sarcomas (RSTS) represent a rare and heterogeneous class of diseases for which the clinical management is still largely non-standardised. Based on a selective review of recent publications, it was the purpose of the present review article to summarize the current concepts of disease classification, diagnostics and surgical as well as multimodal therapy for these tumors.

METHOD

A clinically based empirical review derived from a literature search focusing on publications from the past 5  years was carried out.

RESULTS

Due to the paucity of randomised-controlled trials, therapy for RSTS is largely based on personal experience, retrospectively gathered data and historical controls. Pre-therapeutic planning requires precise information on the localisation, extension, and texture of the tumor through cross-sectional imaging (CT, MRI) as well as histological diagnosis through percutaneous or open biopsy. Complete tumor resection is crucial. Recent studies have confirmed the importance of microscopically negative resection margins which has subsequently led to a trend towards more radical resection. Chemotherapy does not play a role in the adjuvant setting except in clinical trials; however, radiotherapy has been controversely debated in adjuvant RSTS therapy. Efforts to limit radiation toxicity include modern techniques as well as a strategy of using pre-resection radiotherapy instead of postoperative radiation. Surgery is also the treatment of choice for locally recurrent RSTS and pulmonary metastases. The prognosis of RSTS depends on the quality of surgical care and several disease-specific factors (histological type, grading).

CONCLUSION

The clinical management of RSTS is complex and can only partly be considered as evidence-based. Due to the required level of experience in the treatment of these tumor lesions and the involvement of several subspecialties, pre-therapeutic planning, treatment and follow-up should be limited to high-volume surgical centres. In order to achieve microscopically negative resection margins, multivisceral resections are a valuable option after thorough consideration of the risks and benefits. Adjuvant radiotherapy needs to be decided upon on an individual basis, taking into account patient- and tumor-specific factors as well as resection status.

摘要

引言

腹膜后软组织肉瘤(RSTS)是一类罕见且异质性的疾病,其临床管理在很大程度上仍未标准化。基于对近期出版物的选择性回顾,本综述文章旨在总结这些肿瘤的疾病分类、诊断、手术及多模式治疗的当前概念。

方法

进行了一项基于临床的经验性回顾,该回顾源自对过去5年出版物的文献检索。

结果

由于随机对照试验的匮乏,RSTS的治疗在很大程度上基于个人经验、回顾性收集的数据和历史对照。治疗前规划需要通过横断面成像(CT、MRI)精确了解肿瘤的定位、范围和质地,以及通过经皮或开放活检进行组织学诊断。完整切除肿瘤至关重要。近期研究证实了显微镜下切缘阴性的重要性,这随后导致了更激进切除的趋势。除临床试验外,化疗在辅助治疗中不起作用;然而,放疗在RSTS辅助治疗中一直存在争议。限制放射毒性的努力包括现代技术以及采用术前放疗而非术后放疗的策略。手术也是局部复发RSTS和肺转移的首选治疗方法。RSTS的预后取决于手术治疗的质量以及几个疾病特异性因素(组织学类型、分级)。

结论

RSTS的临床管理很复杂,只能部分被视为基于证据。由于治疗这些肿瘤病变所需的经验水平以及涉及多个亚专业,治疗前规划、治疗和随访应限于大型手术中心。为了实现显微镜下切缘阴性,在充分考虑风险和益处后,多脏器切除是一个有价值的选择。辅助放疗需要根据个体情况决定,同时考虑患者和肿瘤特异性因素以及切除情况。

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