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Updated: Jun 29, 2025

Teratoma Generation in the Testis Capsule
Published on: November 7, 2011
Embryonal rhabdomyosarcoma of the testis in a 17-year-old male
Abdikarin Ahmed Mohamed1,2, Aweis Abdullahi Sheik1, Mohamed Abdikarim Nur-Amin2
1Mogadishu Somalia Turkish Training and Research Hospital, Mogadishu, Somalia.
Abstract:
Primary rhabdomyosarcoma of the testis is an exceptionally rare and highly malignant sarcoma. To date, there are only 23 reported cases in the literature. We report a 17-year-old male patient presented with massive scrotal swelling that had been progressively enlarging over seven-months. Scrotal ultrasound and contrast-enhanced CT revealed a 10 × 10cm left testicular heterogeneously enhancing mass that extends into the spermatic cord. A left inguinal orchiectomy was performed, and histopathological examinations showed findings consistent with Rhabdomyosarcoma, Embryonic-type. Primary embryonal testicular rhabdomyosarcoma has poor prognosis, particularly for adolescents, and tumour size greater than 10cm. Early diagnosis and radical orchiectomy improve the prognosis.
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