Abstract
Synchronous multicentric aggressive fibromatosis does not appear to have been previously reported. Two such cases are described. The tumors were identified by magnetic resonance (MR) imaging. The incidence of synchronous multicentric aggressive fibromatosis is not known. It is anticipated that increased use of coronal MR imaging will reveal more tumors of this type, both synchronous and metachronous. In a patient with known or suspected aggressive fibromatosis, every other soft tissue nodule or mass in the same limb has to be regarded as an additional tumor of the same histology.
Similar content being viewed by others
References
Allen PW (1977) The fibromatoses: A clinicopathologic classification based on 140 cases. Part. I. Am J Surg Pathol 1:255
Anonymous-Editorial (1969) The desmoid tumour Br Med J 4:447
Barber HM, Galasko CSB, Woods CG (1973) Multicentric extra-abdominal desmoid tumors. Report of two cases. J Bone Joint Surg [Br] 55:858
Enzinger FM, Weiss SW (1983) Soft tissue tumors. CV Mosby, St. Louis, p 53
Rock MG, Pritchard DJ, Reiman HM, Soule EH, Brewster RC (1984) Extra-abdominal desmoid tumors. J Bone Joint Surg [Am] 66:1369
Sundaram M, McGuire MH, Schajowicz F (1987) Soft tissue masses: Histologic basis for decreased signal (short T2) on T2-weighted MR images. AJR 148:1247
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Sundaram, M., Duffrin, H., McGuire, M.H. et al. Synchronous multicentric desmoid tumors (aggressive fibromatosis) of the extremities. Skeletal Radiol 17, 16–19 (1988). https://doi.org/10.1007/BF00361449
Issue Date:
DOI: https://doi.org/10.1007/BF00361449