Abstract
Desmoid fibromatosis (DF) is a rare intermediate soft tissue tumour characterised by myofibroblastic cell proliferation. Although desmoid tumours are locally very infiltrative, they hold no metastatic potential, and a significant proportion of cases naturally regress if simply observed. Considering this, a first-line policy of active observation should be adopted in all cases (with appropriate analgesia as required). If disease progression or symptoms require intervention, several other non-surgical treatments, including radiotherapy and chemotherapy, should be considered prior to surgery. This makes close collaboration with a soft tissue tumour MDT essential when managing these complex patients.
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Eastley, N.C., Krupa, J., Ashford, R.U. (2018). Desmoid (Aggressive) Fibromatosis of the Breast. In: Wyld, L., Markopoulos, C., Leidenius, M., Senkus-Konefka, E. (eds) Breast Cancer Management for Surgeons. Springer, Cham. https://doi.org/10.1007/978-3-319-56673-3_47
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