ArticleJournal of surgical case reports2025
A 15-year-old male with embryonal rhabdomyosarcoma of the testis-a rare tumor with unusual presentation.
Article in Journal of surgical case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed.
- Paratesticular Embryonal Rhabdomyosarcoma Masquerading as Epididymitis: A Diagnostic Challenge in Adolescents.Clinical case reports · 2026Article
- Metastatic Primary Intratesticular Rhabdomyosarcoma in an Adolescent with Rapid Early Response to VAC Chemotherapy: A Case Report and Literature Review of 99 Cases.Research and reports in urology · 2026Article
Corrections and comments
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Paratesticular embryonal rhabdomyosarcoma (ERMS) is a rare and aggressive mesenchymal tumor with only 24 reported cases in the literature. It is usually seen in children and adolescents presenting as a painless testicular mass. Hereby, we report a 15-year-old male patient who was diagnosed with testicular ERMS during exploratory surgery after testicular trauma. Diagnostic modalities include radiological imaging, histopathological examination, and immunohistochemical analysis. Treatment consists of radical inguinal orchiectomy followed by postoperative chemotherapy and radiotherapy, which has shown promising outcomes in managing this type of tumor.
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