Undifferentiated pleomorphic sarcoma as a rare extracolonic manifestation in Lynch syndrome with MLH1 germline mutation: a case report

Undifferentiated pleomorphic sarcoma (UPS) is a rare and highly aggressive soft tissue sarcoma that typically occurs in the extremities but is rarely found in the retroperitoneal cavity. Despite the documented cases of sarcomas in patients with Lynch syndrome (LS), the relationship between these malignancies and LS has not yet been fully elucidated. In this report, we present the case of a patient with LS who harbored a germline MLH1 loss-of-function mutation (c.2171T>A) and developed synchronous malignancies, including colorectal cancer, cholangiocarcinoma, and retroperitoneal UPS. Consequently, molecular testing revealed mismatch repair deficiency (dMMR) among two cancers, thereby confirming the diagnosis of LS. This case suggests that UPS may represent a rare extracolonic manifestation of LS and highlights the importance of considering MMR/MSI testing in sarcomas of uncertain origin, which may have implications for diagnosis and personalized treatment strategies, including the use of immune checkpoint inhibitors.

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Journal
Frontiers in Oncology
Published
2026-04-21
DOI
https://doi.org/10.3389/fonc.2026.1793258
Primary Topic
Genetic factors in colorectal cancer
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article
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article

Undifferentiated pleomorphic sarcoma as a rare extracolonic manifestation in Lynch syndrome with MLH1 germline mutation: a case report

Yuxing Chen, Mengjiao Wu, Yan Zong, Hongli Liu et al.
Frontiers in Oncology
Genetic factors in colorectal cancer
article

Undifferentiated pleomorphic sarcoma as a rare extracolonic manifestation in Lynch syndrome with MLH1 germline mutation: a case report

Yuxing Chen, Mengjiao Wu, Yan Zong, Hongli Liu, Ruihan Li, Min Jin, Yilin Xiao, Xiaona Chang
article en

Abstract

Undifferentiated pleomorphic sarcoma (UPS) is a rare and highly aggressive soft tissue sarcoma that typically occurs in the extremities but is rarely found in the retroperitoneal cavity. Despite the documented cases of sarcomas in patients with Lynch syndrome (LS), the relationship between these malignancies and LS has not yet been fully elucidated. In this report, we present the case of a patient with LS who harbored a germline MLH1 loss-of-function mutation (c.2171T>A) and developed synchronous malignancies, including colorectal cancer, cholangiocarcinoma, and retroperitoneal UPS. Consequently, molecular testing revealed mismatch repair deficiency (dMMR) among two cancers, thereby confirming the diagnosis of LS. This case suggests that UPS may represent a rare extracolonic manifestation of LS and highlights the importance of considering MMR/MSI testing in sarcomas of uncertain origin, which may have implications for diagnosis and personalized treatment strategies, including the use of immune checkpoint inhibitors.

Frontiers in OncologyVol. 16
Wuhan Union Hospital (CN), Union Hospital (US), Union Hospital (CN), Huazhong University of Science and Technology (CN)
Good health and well-being
Openalex Percentile: Top 21%
Genetic factors in colorectal cancer
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Undifferentiated pleomorphic sarcoma as a rare extracolonic manifestation in Lynch syndrome with MLH1 germline mutation: a case report — Yuxing Chen, Mengjiao Wu, et al. · Frontiers in Oncology (2026) | TGRS Research Map | TGRS