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Subcutaneous leiomyosarcoma of the scrotum mimickering testicular cancer. A case report and literature review

Leiomyosarcoma of the scrotum is a rare tumor. Johnson H Jr in 1987 reported first case. Only 39 cases been reported in the literature. A 74 years old Indian gentleman presented with progressive painless right testicular swelling for 3 months. On examination, a firm right testicular mass. We proceed...

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Detalles Bibliográficos
Autor principal: Hassan, Azmi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7726672/
https://www.ncbi.nlm.nih.gov/pubmed/33318933
http://dx.doi.org/10.1016/j.eucr.2020.101487
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author Hassan, Azmi
author_facet Hassan, Azmi
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description Leiomyosarcoma of the scrotum is a rare tumor. Johnson H Jr in 1987 reported first case. Only 39 cases been reported in the literature. A 74 years old Indian gentleman presented with progressive painless right testicular swelling for 3 months. On examination, a firm right testicular mass. We proceeded with right scrotal exploration with excision of the right scrotal mass. Histopathology showed scrotum leiomyosarcoma. We would like to discuss the rarity of presentation, dilemma of diagnosis and managing in a district hospital. We advocate wide local excision with clear margin of 2 cm which give good overall survival benefits.
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spelling pubmed-77266722020-12-13 Subcutaneous leiomyosarcoma of the scrotum mimickering testicular cancer. A case report and literature review Hassan, Azmi Urol Case Rep Oncology Leiomyosarcoma of the scrotum is a rare tumor. Johnson H Jr in 1987 reported first case. Only 39 cases been reported in the literature. A 74 years old Indian gentleman presented with progressive painless right testicular swelling for 3 months. On examination, a firm right testicular mass. We proceeded with right scrotal exploration with excision of the right scrotal mass. Histopathology showed scrotum leiomyosarcoma. We would like to discuss the rarity of presentation, dilemma of diagnosis and managing in a district hospital. We advocate wide local excision with clear margin of 2 cm which give good overall survival benefits. Elsevier 2020-11-13 /pmc/articles/PMC7726672/ /pubmed/33318933 http://dx.doi.org/10.1016/j.eucr.2020.101487 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Oncology
Hassan, Azmi
Subcutaneous leiomyosarcoma of the scrotum mimickering testicular cancer. A case report and literature review
title Subcutaneous leiomyosarcoma of the scrotum mimickering testicular cancer. A case report and literature review
title_full Subcutaneous leiomyosarcoma of the scrotum mimickering testicular cancer. A case report and literature review
title_fullStr Subcutaneous leiomyosarcoma of the scrotum mimickering testicular cancer. A case report and literature review
title_full_unstemmed Subcutaneous leiomyosarcoma of the scrotum mimickering testicular cancer. A case report and literature review
title_short Subcutaneous leiomyosarcoma of the scrotum mimickering testicular cancer. A case report and literature review
title_sort subcutaneous leiomyosarcoma of the scrotum mimickering testicular cancer. a case report and literature review
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7726672/
https://www.ncbi.nlm.nih.gov/pubmed/33318933
http://dx.doi.org/10.1016/j.eucr.2020.101487
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