Case ReportInternational Journal of Research in Medical Sciences
Publication: Primary intratesticular rhabdomyosarcoma: a rare aggressive childhood neoplasm
Int J Res Med Sci. 2020;8(3):1148-1151.DOI10.18203/2320-6012.ijrms20200795
Abstract
Testicular tumors are relatively uncommon in children. The tumors of germ cell origin are still frequently encountered. The pure embryonal rhabdomyosarcomas of testis, not associated with sarcomatous component of the germ cell tumor, is a very rare entity. It is a highly aggressive tumor of childhood and young adolescents. In testes, it arises commonly from paratesticular tissue; primary intratesticular being extremely rare. To the best of authors knowledge, only fifteen cases of primary pure intratesticular tumor have been reported in the literature so far. We report a case of eight-year-old child who presented with a progressive painless right testicular enlargement over two months. Ultrasonography showed a heterogenous intratesticular mass. High orchidectomy was performed. Histopathological examination of the specimen assisted with immunohistochemistry revealed embryonal rhabdomyosarcoma.
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Affiliations
- Department of Pathology, Teerthanker Mahaveer Medical College & Research Centre, Moradabad, Uttar Pradesh, India
- Department of Pathology, Shaheed Hasan Khan Mewati Government Medical College, Nuh, Mewat, Haryana, India
- Department of Surgery, Shri Guru Ram Rai Institute of Medical and Health Sciences, Patel Nagar, Dehradun, Uttarakhand, India
