Publisher's Synopsis
Soft-tissue sarcomas of the limbs are rare malignant tumors arising from connective tissue. Their rarity, the diversity of histological types and localizations, and the heterogeneity of the evolutionary risk make their diagnosis and treatment an extremely difficult undertaking, with many uncertainties. The aim of this study was to examine the epidemiological, clinical, radiological and pathological features of soft tissue sarcomas, as well as the various diagnostic and therapeutic stages, in order to establish recommendations for standardizing and improving the management of these tumors. Our study was retrospective, covering a period of 11 years. The mean follow-up period was 42 months. Clinical, radiological and anatomopathological data, together with the results of treatment, were analyzed and compared with the literature. The management of soft tissue sarcomas must be carried out in a referral center and be part of a true therapeutic strategy involving a multidisciplinary team in order to ensure optimal results.
