Desmoid tumours

被引:178
作者
Shields, CJ [1 ]
Winter, DC [1 ]
Kirwan, WO [1 ]
Redmond, HP [1 ]
机构
[1] Natl Univ Ireland Cork, Cork Univ Hosp, Acad Dept Surg, Cork, Ireland
来源
EUROPEAN JOURNAL OF SURGICAL ONCOLOGY | 2001年 / 27卷 / 08期
关键词
desmoid tumour; fibromatosis; Gardner's syndrome; familial adenomatous polyposis; tamoxifen;
D O I
10.1053/ejso.2001.1169
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Desmoid tumours exhibit fibroblastic proliferation and arise from fascial or musculoaponeurotic structures. Despite their benign microscopic appearance, and their negligible metastatic potential, the propensity of desmoid tumours for local infiltration is potentially significant in terms of deformity, morbidity and mortality due to pressure effects and obstruction of vital structures and organs. The rarity of desmoid tumours, coupled with the variability in their clinical course, renders these lesions a vexing entity, and makes demonstration of the efficacy of any specific intervention difficult. Failure to recognize the potential for malignant behaviour in this tumour renders desmoids susceptible to inadequate treatment. This distinct pathological entity is reviewed with a specific focus on aetiology and treatment. (C) 2001 Harcourt Publishers Ltd.
引用
收藏
页码:701 / 706
页数:6
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