Soft Tissue Tumors of the Abdomen and Retroperitoneum

被引：7

作者：

Turgeon, Michael K. ^{[1
]}

Cardona, Kenneth ^{[2
]}

机构：

[1] Emory Univ, Div Surg Oncol, Dept Surg, Winship Canc Inst, 1365 Clifton Rd Northeast,Bldg B,Suite 4100, Atlanta, GA 30322 USA

[2] Emory Univ, Winship Canc Inst, Dept Surg, Div Surg Oncol, 550 Peachtree St,Northeast,9th Floor,Suite 900, Atlanta, GA 30308 USA

来源：

SURGICAL CLINICS OF NORTH AMERICA | 2020年 / 100卷 / 03期

关键词：

Retroperitoneal sarcoma; Desmoid tumors; Surgery; Multimodality therapy; Active surveillance; FAMILIAL ADENOMATOUS POLYPOSIS; DESMOID-TYPE FIBROMATOSIS; INTERMEDIATE-GRADE; PROGNOSTIC FACTORS; BEAM RADIOTHERAPY; SARCOMA PATIENTS; FREE SURVIVAL; MANAGEMENT; LIPOSARCOMA; SURGERY;

D O I：

10.1016/j.suc.2020.02.011

中图分类号：

R61 [外科手术学];

学科分类号：

摘要：

Soft tissue tumors of the abdomen and retroperitoneum encompass a wide range of benign and malignant neoplasms. Retroperitoneal sarcomas, the most common, are composed of rare malignancies with numerous histiotypes. Surgery remains the cornerstone of treatment and the only curative option for retroperitoneal sarcomas. With histiotype-dependent local and distant recurrences, it is imperative these cases are discussed in a multidisciplinary tumor board setting at specialized sarcoma centers. This review discusses the current evidence for the management of abdominal and retroperitoneal soft tissue tumors, with particular focus on retroperitoneal sarcomas and desmoid tumors.

引用

页码：649 / 667

页数：19

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