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Acta médica Grupo Ángeles

versión impresa ISSN 1870-7203

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FLORES PALOMAR, Francisco José et al. Lower extremity synovial sarcoma. Acta méd. Grupo Ángeles [online]. 2020, vol.18, n.1, pp.83-86.  Epub 22-Mar-2022. ISSN 1870-7203.  https://doi.org/10.35366/92007.

Synovial sarcoma is a malignant mesenchymal neoplasm. Its typical presentation is a juxtaarticular mass, palpable and painless. We present a 63 years old male, with a tumor in the left inguinal region, an excisional biopsy was performed, resulting in a hydradenocarcinoma with a positive regional ganglion. Immunohistochemistry was performed resulting in poorly differentiated synovial sarcoma. Synovial sarcoma is a rare soft tissue neoplasm affecting young adults. It is located more frequently in the extremities and the presence of metastasis at diagnosis is common. It has a poor prognosis and the treatment is with surgical resection and chemotherapy.

Palabras llave : Synovial Sarcoma; soft-tissue tumor; inferior limb.

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