An extremely rare case of testicular malign neoplasm; alveolar subtype of rhabdomyosarcoma with long term follow-up.

Authors

  • Tumay Ipekci Department of Urology, Baskent University Alanya Research Hospital, Alanya, Antalya, Turkey.
  • Yigit Akin Department of Urology, Harran University School of Medicine, Sanliurfa
  • Burak Hoscan Department of Urology, Baskent University Alanya Research Hospital, Alanya, Antalya, Turkey.
  • Ahmet Tunckiran Department of Urology, Baskent University Alanya Research Hospital, Alanya, Antalya, Turkey.

DOI:

https://doi.org/10.17532/jhsci.2014.196

Keywords:

testis, neoplasm, rhabdomyosarcoma

Abstract

Testicular neoplasm usually occur in men aged between 15 and 35. These are solid organ tumours and also should be operated when there is a suspicious clinical findings. Testis tumours are levelled after histopathology evaluation. The medical, surgical and follow-up strategies of well know testis tumours, such as seminomas, non-seminom germ cell tumours, have been established. In case of testis tumours rare entities may occur as rhabdomyosarcoma.

We here presented a rare case of   alveolar subtype of rhabdomyosarcoma in testis with long term follow-up.

Downloads

Download data is not yet available.

Downloads

Published

27.09.2014

Issue

Section

Letters to Editor

How to Cite

1.
An extremely rare case of testicular malign neoplasm; alveolar subtype of rhabdomyosarcoma with long term follow-up. JHSCI [Internet]. 2014 Sep. 27 [cited 2024 Apr. 25];4(2):134-5. Available from: https://www.jhsci.ba/ojs/index.php/jhsci/article/view/150