Intratesticular Rhabdomyosarcoma- A Rare Childhood Tumour

Authors

  • Hilda Fernandes Department of Pathology, Fr Muller Medical College, Mangalore, India
  • Netheya Mary Thomas Department of Pathology, Fr Muller Medical College, Mangalore, India
  • Anush Serrao Department of Pathology, Fr Muller Medical College, Mangalore, India

DOI:

https://doi.org/10.21276/apalm.3137

Keywords:

testis, embryonal, rhabdomyosarcoma

Abstract

Primary malignant of tumours of the testis are rare in children. Tumours of germ cell origin account for 60-77% of primary testicular tumors. Intrascrotal tumours of nongerm cell origin are rare. Rhabdomyosarcomas (RMS) are the commonest tumours among nongerm cell tumours. RMS are more commonly seen in paratesticular region. Pure testicular RMS are rare. A 16 yr boy was evaluated right sided testicular mass. Histopathology and immunohistochemistry confirmed it to be an anaplastic embryonal rhabdomyosarcoma. Here we report this case with a brief review of literature.

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Published

31-03-2022

How to Cite

1.
Fernandes H, Thomas NM, Serrao A. Intratesticular Rhabdomyosarcoma- A Rare Childhood Tumour. Ann of Pathol and Lab Med [Internet]. 2022 Mar. 31 [cited 2024 Nov. 19];9(3):C24-27. Available from: https://pacificejournals.com/journal/index.php/apalm/article/view/3137

Issue

Section

Case Report