A case of children with primary intratesticular rhabdomyosarcoma

In children, the most typical soft tissue tumor is a rhabdomyosarcoma (RMS). A primary intratesticular rhabdomyosarcoma is quite uncommon. An eleven-year-old had a painless left testicular tumor for two months. The patient's left scrotum was found to have a firm, non-tender lump. A massive hypo...

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Detalles Bibliográficos
Autores principales: Majid, Ghani Ikhsan, Rachmadiyan, Alyadi, Octavian, Irvan, Karim, M. Ilhamul, Mardianty, Friska
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Oncology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9720432/
https://www.ncbi.nlm.nih.gov/pubmed/36478963
http://dx.doi.org/10.1016/j.eucr.2022.102293
Descripción
Sumario:In children, the most typical soft tissue tumor is a rhabdomyosarcoma (RMS). A primary intratesticular rhabdomyosarcoma is quite uncommon. An eleven-year-old had a painless left testicular tumor for two months. The patient's left scrotum was found to have a firm, non-tender lump. A massive hypoechoic intratesticular mass measuring 8.0 × 7.5 × 6.0 cm was found in the left scrotum by scrotal and abdominal ultrasonography. The patient had an inguinal orchiectomy. Histopathological examination disclosed botryoid rhabdomyosarcoma. Primary intratesticular rhabdomyosarcomas are rare. Radical orchiectomy and chemotherapy are recommended. It may increase overall and disease-free survival.

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