• 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