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Updated: Jul 7, 2026
Tumorsphere Derivation and Treatment from Primary Tumor Cells Isolated from Mouse Rhabdomyosarcomas
Published on: September 13, 2019
[Paratesticular mixed sarcoma: liposarcoma-rhabdomyosarcoma. Case report and bibliographic review]
Arturo Astigueta Pérez1, Mariela Pow-Sang Godoy, Milagros Abad Licham
1Departamento de Urología Oncológica, Instituto Nacional de Enfermedades Neoplásicas, Lima, Perú.
Objective:
Sarcomas arising from the urinary tract are rare, representing less than 2% of all urologic tumors. The paratesticular region is one of the most unfrequent locations. Leiomyosarcoma, rhabdomyo-sarcoma, liposarcoma, malignant fibrohistiocytoma, etc. and the combination of two or more histological types has exceptionally been reported. We describe the case of a patient with a mixed paratesticular sarcoma and perform a bibliographic review.
Methods:
The patient underwent right radical orchyectomy and the surgical specimen was sent to pathologic study.
Results:
There are no previous case reports in the literature of paratesticular mixed tumor with liposarcoma and rhabdomyosarcoma.
Conclusions:
Sarcomas of the spermatic cord are rare neoplasias and should be considered on the differential diagnosis of scrotal masses. The treatment of choice is surgical and adjuvant treatment must be individualized depending on tumor aggressiveness.
