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THE RAREST FORM OF PARATESTICULAR LEIOMYOSARCOMA
1Department of Urology, Hereford County Hospital, Wye Valley NHS Trust
Paratesticular tumours make up less than 5% of intra-scrotal tumours and of these, approximately 30%are malignant tumours with sarcomas accounting for the majority.
Leiomyosarcoma is a malignant tumour arising from soft tissues containing smooth muscle. They are reported as comprising between 5-30% of paratesticular sarcomas.1,2 It is extremely rare that they arise from tissue other than the spermatic cord or epididymis.
The authors describe such a case of paratesticular leiomyosarcoma in a 54-year-old man who presented with a six-month history of a painful testis and who subsequently underwent radical inguinal orchidectomy and high ligation.
Jonathan Cobley. THE RAREST FORM OF PARATESTICULAR LEIOMYOSARCOMA. Journal of Men's Health. 2018. 14(1);19-21.
1. Husain M and Verma N. Current concepts in pa-thology of soft tissue sarcoma. Indian J Surg Oncol 2011;2(4):302–3. Available at: https://www.ncbi.nlm. nih.gov/pmc/articles/PMC3338140/
2. Unlu Y et al. Paratesticular sarcomas: a report of seven cases. Oncol Lett 2015;9:308–12. Available at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4246635/
3. Galosi AB et al. Adult primary paratesticular mesen-chymal tumors with emphasis on a case presentation and discussion of spermatic cord leiomyosarcoma. Diagnost Pathol 2014;9:90. Available at: https://www. ncbi.nlm.nih.gov/pmc/articles/PMC4039061/
4. Khoubehi B, et al. Adult paratesticular tumours. BJU Internat 2002;90:707–15. Available at: http://onlinelibrary. wiley.com/doi/10.1046/j.1464-410X.2002.02992.x/full
5. Haran S, Balakrishnan V, Neerhut G. A rare case of paratesticular leiomyosarcoma. Case Rep Urol 2014. Available at: https://www.hindawi.com/journals/criu/2014/715395/
6. Patel B, Vora A, Muruve N. Case of subcutaneous leio-myosarcoma of the scrotum presenting as a sebaceous cyst in a 71-year-old man: a case report and review of the literature. Urol Case Rep 2014;2:181–82. Avail-able at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4782121/
7. Sighinolfi MC, et al. Well-differentiated giant scrotal liposarcoma: case presentation and management. Andro-logia 2008;40:200–202. Available at: http://onlinelibrary. wiley.com/doi/10.1111/j.1439-0272.2008.00841.x/full
8. Bansal D, et al. Leiomyosarcoma presenting as a scrotal mass. Urol Case Rep 2016;7:42–44. Available at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4909635/
9. Alfarelos J et al. Paratesticular leiomyosarcoma: a case report and review of the literature. Urol Case Rep 2017;11:30–32. Available at: https://www.ncbi.nlm.nih. gov/pmc/articles/PMC5225278/
10. Kyratzi I, et al. Imaging features of a huge spermatic cord leiomyosarcoma: Review of the literature. World J Radiol 2011;3(4):114–19. Available at: https://www. ncbi.nlm.nih.gov/pmc/articles/PMC3084435/
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