AGGRESSIVE FIBROMATOSIS (NONFAMILIAL DESMOID TUMOR) - THERAPEUTIC PROBLEMS AND THE ROLE OF ADJUVANT RADIOTHERAPY

Citation
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
Citations number
35
Categorie Soggetti
Surgery
Journal title
ISSN journal
00071323
Volume
82
Issue
4
Year of publication
1995
Pages
510 - 514
Database
ISI
SICI code
0007-1323(1995)82:4<510:AF(DT->2.0.ZU;2-5
Abstract
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.