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Case Report
Copyright ©The Author(s) 2026. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Clin Cases. Feb 26, 2026; 14(6): 118138
Published online Feb 26, 2026. doi: 10.12998/wjcc.v14.i6.118138
Undifferentiated testicular pleomorphic sarcoma: A case report
Jordan Sarver, Ali Baydoun, Marko Gudziak
Jordan Sarver, Ali Baydoun, Department of Urology, Detroit Medical Center, Detroit, MI 48201, United States
Marko Gudziak, Department of Urology, Michigan Institute of Urology, Pontiac, MI 48341, United States
Author contributions: Sarver J, Baydoun A, and Gudziak M performed the research, contributed ideas, analyzed the data, and wrote the manuscript; Sarver J revised the manuscript. All authors have read and approved the final manuscript.
Informed consent statement: The patient signed an informed consent statement.
Conflict-of-interest statement: All the authors report no relevant conflicts of interest for this article.
CARE Checklist (2016) statement: The authors have read the CARE Checklist (2016), and the manuscript was prepared and revised according to the CARE Checklist (2016).
Open Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/
Corresponding author: Jordan Sarver, Department of Urology, Detroit Medical Center, Harper Professional Building 4160 John R St. Suite 1017, Detroit, MI 48201, United States. j.sarver1011@gmail.com
Received: December 25, 2025
Revised: January 11, 2026
Accepted: February 4, 2026
Published online: February 26, 2026
Processing time: 50 Days and 23.1 Hours
Core Tip

Core Tip: Testicular sarcomas are a rare type of soft tissue sarcoma. The standard treatment of the testicular mass usually begins with radical inguinal orchiectomy. Patients with scrotal sarcomas are at high risk of local and distant recurrence, emphasizing the importance of surgical excision and wide margins. There is little studied regarding the integration of radiotherapy and chemotherapy for these cases as neoadjuvant or adjuvant therapies. This case highlights the presentation and treatment of a patient with a rare phenotype of testicular pleomorphic sarcoma treated by radical inguinal orchiectomy.