METASTATIC RECURRENCE OF PARA TESTICULAR RHABDOMYOSARCOMA: ABOUT A CASE WITH REVIEW OF THE LITERATURE
*K. Mazouz, M. Saadoun, M. Raouah Y. Ammor, S. Barkich, H. Abourazzek, H. Eddaoualline, H. Sami, A. Zayan, D. Nimbuna, Z. Kaitoni, A. Elmatlini, M. Laanigri, Y. Bouchabaka, S. Laatitioui, M. Darfaoui, I. Lalya, A. El Omrani and M. Khouchani
Para-testicular rhabdomyosarcoma (RMS) is a rare mesenchymal tumor that can develop from the spermatic cord, epididymis or testicular vaginal. It constitutes 7% of cases of rhabdmyosarome The diagnosis requires histological confirmation. The treatment must be multimodal in view of the aggressiveness of these tumors, based on surgery, chemotherapy and radiotherapy. We report the observation of a paratesticular rhabdomyosarcoma case in metastatic recurrence. In the light of these clinical data we will discuss the diagnostic and therapeutic modalities.
Keywords: Para-testicular rhabdomyosarcoma (RMS) is a rare mesenchymal modalities.
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