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CASE REPORT

A rare case report of paratesticular leiomyosarcoma

Santosh Nimkar1 ,  Bianca Glass1 ,  Samir Dalia2*
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1 College of Osteopathic Medicine, Kansas City University, Joplin, Missouri, United States of America
2 Department of Medical Oncology, Mercy Hospital, Joplin, Missouri, United States of America
CP 2024, 6(3), 3971
Submitted: 18 June 2024 | Accepted: 8 July 2024 | Published: 29 August 2024
© 2024 by the Author(s). This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution 4.0 International License ( https://creativecommons.org/licenses/by/4.0/ )
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Abstract

A leiomyosarcoma (LMS) is a malignant mesenchymal tumor of soft tissue that rarely presents in the scrotal region. This case report describes a primary paratesticular LMS originating in the dartos layer of the scrotum in a symptomatic 37-year-old male with a history of hypertension, generalized seizure disorder post-excision of meningioma, and an extensive family history of cancer. Primary paratesticular LMSs in the superficial dartos layer are exceedingly rare. Given the rarity of this particular type of LMS, this case report includes a discussion on its prevalence and incidence. The rarity of this tumor also warrants a review of the literature and related cases to inform the treatment plan and enhance understanding of these oncologic conditions.

Keywords
Paratesticular leiomyosarcoma
Testicular leiomyosarcoma
Paratesticular cancer
Testicular cancer
Leiomyosarcoma
Sarcoma
Funding
None.
Conflict of interest
The authors declare that they have no competing interests.
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Cancer Plus, Electronic ISSN: 2661-3840 Print ISSN: 2661-3832, Published by AccScience Publishing
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