Jt. Plukker et al., AGGRESSIVE FIBROMATOSIS (NONFAMILIAL DESMOID TUMOR) - THERAPEUTIC PROBLEMS AND THE ROLE OF ADJUVANT RADIOTHERAPY, British Journal of Surgery, 82(4), 1995, pp. 510-514
Aggressive fibromatosis is a rare soft tissue tumour with a high tende
ncy to local recurrence, even after apparently adequate resection. Wid
e local excision with a margin of at least 3 cm, depending on the anat
omical location, should be performed to improve rates of recurrent dis
ease. There is no consensus concerning the role of radiotherapy in the
treatment of these lesions. The clinical findings of 39 cases diagnos
ed between 1972 and 1991 were reviewed retrospectively. Local control
was effected in 19 of 32 patients treated with surgery alone after a m
edian (range) follow-up of 72 (18-236) months. There were 40 cases of
recurrent fibromatosis in 15 patients. Local control was obtained in 1
3 of 14 patients who received radiotherapy using a wide-field techniqu
e and doses of more than 50 Gy over a period of 5 weeks after marginal
or incomplete resection of primary or recurrent lesions (P < 0.001).
The results suggest that in a selected group of patients with aggressi
ve fibromatosis radiotherapy may effectively achieve control of residu
al disease after surgery without marked disfigurement and loss of func
tion.