Recent Trends in the Management of Desmoid Tumors
- 1 December 1989
- journal article
- review article
- Published by Wolters Kluwer Health in Annals of Surgery
- Vol. 210 (6) , 765-769
- https://doi.org/10.1097/00000658-198912000-00012
Abstract
Recent advances in the understanding of desmoid tumor biology affect therapeutic choices. This series of 19 patients and review of the literature outlines historic perspectives and discusses the options in the management of these locally aggressive tumors. Desmoid tumors tend to grow steadily, regardless of tumor location. However differences in the aggressive nature of these tumors are seen when age and sex distributions are scrutinized. Although recurrence rates are high, excisional therapy is the best first approach. An exception is the case in which tumor excision is either particularly dangerous or likely to result in significant physical handicap. Radiation or drug therapy are most often used with recurrent disease or as an alternative to mutilating surgery. Although many pharmacologic approaches have been advocated, (including antiestrogen therapy, cyclic-AMP, and prostaglandin inhibition), results are anecdotal at best.Keywords
This publication has 17 references indexed in Scilit:
- The desmoid syndromeThe American Journal of Surgery, 1986
- Extra-abdominal desmoid tumorsActa Orthopaedica, 1986
- Desmoid tumors and their managementThe American Journal of Surgery, 1985
- Extra-abdominal desmoid tumors.Journal of Bone and Joint Surgery, 1984
- Radiation therapy in the treatment of aggressive fibromatoses (desmoid tumors)Cancer, 1984
- Mesenteric desmoid tumor in Gardner's syndrome treated by sulindacDiseases of the Colon & Rectum, 1984
- Indomethacin and ascorbate inhibit desmoid tumorsJournal of Surgical Oncology, 1980
- Alteration of tumor growth by aspirin and indomethacin: Studies with two transplantable tumors in mouseEuropean Journal of Pharmacology, 1976
- The occurrence of desmoids in patients with familial polyposis coliBritish Journal of Surgery, 1970
- DESMOID TUMOURS. A SERIES OF 33 CASES.1963