Soft tissue sarcomas (STS) are a rare and diverse group of malignancies that account for
approximately 1% of all adult cancers [1]. In Europe, the estimated incidence is 4-5 cases …

Abstract Background and Purpose: Retroperitoneal lymph node dissection (RPLND) is
recommended in children 10 years or older with paratesticular rhabdomyosarcoma …

Background Paratesticular leiomyosarcoma (LMS) is a rare tumor. Conventionally, tumor
resection by high inguinal orchiectomy is performed as the preferred treatment approach for …

10070 Background: Five-year overall survival (OS) of localized RMS of children< 18
exceeds 70%, while OS in adult pts is poor. We report a retrospective experience from …

Objectives To report one case of metastatic paratesticular rhabdomyosarcoma in a 14 years
old patient, classified as stage IIb (IRSG). Methods After treatment with radical surgery …

Para-testicular rhabdomyosarcoma (PTRMS) is a rare tumor, and it accounts for 7% of all
rhabdomyosarcoma tumors. Among all the rhabdomyosarcoma (RMS) types, the spindle cell …

Results: The median age of the patients was 16.5 years. The median duration of symptoms
was 5 months. Five patients had retroperitoneal lymphadenopathy (RPLAP) while three had …

Rhabdomyosarcomas (RMS) originate from immature cells capable of differentiating into
skeletal muscle cells and commonly emerge in the skeletal muscle, orbit, nose, anus, testis …

Methods: We aim to perform a systematic review and meta-analysis of the available data in
the last 50 years in a methodologically rigorous and transparent manner to identify patterns …

The large number of patients entered into the Intergroup Rhabdomyosarcoma Study (IRS)
has allowed a study of prognostic factors and clinical management decisions for a specific …