Journal Basic Info

  • Impact Factor: 2.709**
  • H-Index: 11 
  • ISSN: 2474-1663
  • DOI: 10.25107/2474-1663
**Impact Factor calculated based on Google Scholar Citations. Please contact us for any more details.

Major Scope

  •  Pancreatic Cancer
  •  Surgical Oncology
  •  Colorectal Cancer
  •  Chemoprevention
  •  Kidney Cancer
  •  Brain and Spinal Cord Cancer
  •  Carcinomas
  •  Bladder Cancer


Citation: Clin Oncol. 2016;1(1):1094.DOI: 10.25107/2474-1663.1094

A Case Report of Paratesticular Rhabdomyosarcoma in an Adolescent

Shazly AR, Abd M and Shazly MU

Urology and Nephrology Center, Menoufia University Hospital, Egypt
Department of Urology, Menoufia University, Egypt

*Correspondance to: Shazly MU 

 PDF  Full Text Case Report | Open Access


Rhabdomyosarcoma (RMS) is a malignant tumor of mesenchymal origin typically affects children and adolescents, with an annual incidence of 4.3 cases per 1 million population aged <20 years. Para testicular RMS is rare, constituting 4-7% of all RMS in children and young adults. Here we report a case of 16-year old boy with right paratesticular solid mass. Ultrasound revealed vascular paratesticular mass separated from the testis. Right Inguinal orchiectomy was done. Histopathology revealed embryonal Rhabdomyosarcoma (a plastic variant) infiltrating fascia of the spermatic cord. There was no lymph node infiltration or distant metastasis in further work up.


Cite the Article:

Shazly AR, Abd M, Shazly MU. A Case Report of Paratesticular Rhabdomyosarcoma in an Adolescent. Clin Oncol. 2016; 1: 1094.

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