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- W1996992025 startingPage "31" @default.
- W1996992025 abstract "Paratesticular rhabdomyosarcoma (RMS) is a rare tumor arising from the mesenchymal tissues of the spermatic cord, epididymis, testis and testicular tunics. It represents only 7% of all patients entered in the Intergroup Rhabdomyosarcoma Study (IRS) and 17% of all malignant intrascrotal tumors in children less than 15 years old. We report a case of a 13-year-old male with left paratesticular RMS who was treated successfully with surgery and systemic chemotherapy. The patient is disease-free after 7 years of treatment completion." @default.
- W1996992025 created "2016-06-24" @default.
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- W1996992025 date "2012-01-01" @default.
- W1996992025 modified "2023-09-26" @default.
- W1996992025 title "Long term survival in paratesticular rhabdomyosarcoma" @default.
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- W1996992025 doi "https://doi.org/10.4103/2278-0513.95017" @default.
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