Abstract
Paratesticular rhabdomyosarcomas are rare tumors with aggressive growth patterns. Multimodal therapy with surgery, chemotherapy, and radiotherapy provides the patient with an excellent long-term prognosis. These tumors often present in the first two decades after birth. We report on the case of an 18-year-old man with a paratesticular rhabdomyosarcoma.
MeSH terms
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Adolescent
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Diagnosis, Differential
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Humans
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Male
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Rhabdomyosarcoma, Embryonal / complications
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Rhabdomyosarcoma, Embryonal / diagnosis*
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Rhabdomyosarcoma, Embryonal / pathology
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Testicular Hydrocele / complications
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Testicular Hydrocele / diagnosis*
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Testicular Neoplasms / complications
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Testicular Neoplasms / diagnosis*
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Testicular Neoplasms / pathology