RHABDOMYOSARCOMA IN A 16-YEAR-OLD BOY: A RARE CASE REPORT

Main Article Content

Nadeem bin Nusrat
Assad ur Rehman
Nauman Zafar
Shujah Muhammad
Sarmad Imtiaz Bajwa
Saira Imtiaz

Abstract

The urinary bladder is a prominent site for rhabdomyosarcoma (RMS), the second most common malignant soft tissue sarcoma in children and adolescents after osteosarcoma. RMS is an uncommon and occasionally fatal malignancy that affects youngsters. Despite extensive treatment plans that combine radiation therapy, dose-intensive combination chemotherapy, and surgery, the prognosis for individuals with metastatic disease is still dismal.


Keywords:  Immunohistochemical findings, Rhabdomyosarcoma, Urinary bladder.

Article Details

How to Cite
Nusrat, N. bin, Rehman, A. ur, Zafar, N., Muhammad, S. ., Bajwa, S. I., & Imtiaz, S. (2024). RHABDOMYOSARCOMA IN A 16-YEAR-OLD BOY: A RARE CASE REPORT. Journal of Medical Sciences, 32(1), 105–107. Retrieved from https://jmedsci.com/index.php/Jmedsci/article/view/1752
Section
Case Report

Most read articles by the same author(s)