Title of article :
Desmoid tumours
Author/Authors :
C. J. Shields، نويسنده , , D. C. Winter، نويسنده , , W. O. Kirwan، نويسنده , , H. P. Redmond، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2001
Pages :
6
From page :
701
To page :
706
Abstract :
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.
Keywords :
desmoid tumour , fibromatosis , Gardnerיs syndrome , familial adenomatous polyposis , tamoxifen.
Journal title :
European Journal of Surgical Oncology
Serial Year :
2001
Journal title :
European Journal of Surgical Oncology
Record number :
510451
Link To Document :
بازگشت