Spermatic cord leiomyosarcoma in a young male: a case report and literature review

Authors

  • Muhammad Sohaib Nadeem Department of Clinical Oncology, Combined Military Hospital, Rawalpindi, Pakistan
  • Kashif Ali Sarwar Department of Radiation Oncology, Combined Military Hospital, Rawalpindi, Pakistan
  • Ujala Ali Department of Physiology, Army Medical College, Rawalpindi, Pakistan

DOI:

https://doi.org/10.47391/JPMA.4137

Abstract

Spermatic cord Leiomyosarcoma is an extremely rare intrascrotal tumour. Owing to its rarity, no definitive management guidelines have been formulated as yet. The majority of published literature comprises of case reports or case series and show varying outcomes depending upon multiple patient- and disease-related factors. Almost all cases are older adults with majority in the sixth or seventh decades of life. It is commonly labelled as an indolent curable tumour if treated early by radical orchiectomy. The role of lymphadenectomy, adjuvant radiotherapy or chemotherapy is unclear.

This case report concerns a young 38-year-old man who suffered from a painless firm left hemiscrotal mass for the past two years. Ultrasonography showed an intrascrotal paratesticular mass. Metastatic workup was negative. Left radical orchiectomy was performed and histopathology of the surgical specimen revealed leiomyosarcoma of the spermatic cord.

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Published

2022-12-15

Issue

Section

Case Report