Retroperitoneal liposarcoma a case report of a rare mesenchymal tumor
Case Report
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https://doi.org/10.58372/2835-6276.1200Keywords:
Retroperitoneal , liposarcoma , mesenchymal tumorAbstract
Retroperitoneal liposarcoma is a rare clinical entity characterized by its initial asymptomatic development and its progressive increase in size leading to compression of neighboring organs, thus constituting the most frequent mode of revelation. Surgery is the only potentially curative treatment. The use of neoadjuvant or adjuvant chemotherapy and/or radiotherapy is controversial due to the low sensitivity of these tumors. Despite adequate management of the tumor, the risk of recurrence is high, often necessitating one or more additional resections.
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