Prise en charge des sarcomes des tissus mous abdominaux [Management of abdominal soft tissue sarcomas]
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16 juin 2021
- doi: 10.53738/REVMED.2021.17.743.1172
- issn: 1660-9379
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info:eu-repo/semantics/altIdentifier/doi/10.53738/REVMED.2021.17.743.1172
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info:eu-repo/semantics/altIdentifier/pmid/34133095
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info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_B1CF53F8316E3
info:eu-repo/semantics/openAccess , CC BY-NC-ND 4.0 , https://creativecommons.org/licenses/by-nc-nd/4.0/
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R. Djafarrian et al., « Prise en charge des sarcomes des tissus mous abdominaux [Management of abdominal soft tissue sarcomas] », Serveur académique Lausannois, ID : 10.53738/REVMED.2021.17.743.1172
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Sarcomas are rare tumors divided into two categories: soft tissue sarcomas and bone sarcomas. A soft tissue mass measuring more than 5 cm, deep, growing, atypical or symptomatic should be investigated further and referred to a specialized center. A percutaneous image-guided biopsy should always be performed in suspicious cases. Standard treatment is surgical. Radiotherapy and chemotherapy should be discussed in a multidisciplinary meeting. Recurrence is frequent and close follow-up of patients over the long term is necessary. A high degree of suspicion is required for any atypical abdominal lesion and the patient should be referred to a specialized sarcoma center as soon as possible instead of performing a surgical biopsy.