A Case Report of Pancreatic Oligometastasis of Uterine Leiomyosarcoma.

IF 0.6 Q4 ONCOLOGY
Case Reports in Oncological Medicine Pub Date : 2026-04-15 eCollection Date: 2026-01-01 DOI:10.1155/crom/1838527
Anne Cambrelin, Sydney Oesch, Brian Orr, Chelsea Wooster, David Lewin, Justin Harold
{"title":"A Case Report of Pancreatic Oligometastasis of Uterine Leiomyosarcoma.","authors":"Anne Cambrelin, Sydney Oesch, Brian Orr, Chelsea Wooster, David Lewin, Justin Harold","doi":"10.1155/crom/1838527","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Uterine leiomyosarcoma (uLMS) is a rare, aggressive uterine malignancy with poor prognosis due to its early hematogenous spread, typically to the lungs and liver, and high recurrence rate. Pancreatic metastases are exceptionally rare, and isolated involvement of the pancreas is even more uncommon.</p><p><strong>Case: </strong>An 81-year-old patient was admitted after an unwitnessed fall and new neurologic symptoms, later diagnosed as a cerebellar stroke. Abdominopelvic imaging for urinary retention revealed a 9.9 × 15.1 × 18.8 - cm heterogeneous uterine mass and a 1.9-cm hypoenhancing lesion in the pancreatic head. Pelvic MRI findings suggested uLMS. Endoscopic ultrasound-guided biopsy confirmed the pancreatic lesion as metastatic leiomyosarcoma. No other sites of metastatic disease were found. Due to her extensive comorbidities and limited performance status, the patient ultimately elected for hospice care after being thoroughly counseled on her treatment options and multidisciplinary consultation.</p><p><strong>Conclusion: </strong>This case illustrates a rare instance of isolated pancreatic metastasis from primary uLMS, a presentation that can mimic primary pancreatic cancer. It emphasizes the need for a broad differential diagnosis, histologic confirmation, and individualized treatment planning in medically complex patients.</p>","PeriodicalId":9636,"journal":{"name":"Case Reports in Oncological Medicine","volume":"2026 ","pages":"1838527"},"PeriodicalIF":0.6000,"publicationDate":"2026-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13080261/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Case Reports in Oncological Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/crom/1838527","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/1 0:00:00","PubModel":"eCollection","JCR":"Q4","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Uterine leiomyosarcoma (uLMS) is a rare, aggressive uterine malignancy with poor prognosis due to its early hematogenous spread, typically to the lungs and liver, and high recurrence rate. Pancreatic metastases are exceptionally rare, and isolated involvement of the pancreas is even more uncommon.

Case: An 81-year-old patient was admitted after an unwitnessed fall and new neurologic symptoms, later diagnosed as a cerebellar stroke. Abdominopelvic imaging for urinary retention revealed a 9.9 × 15.1 × 18.8 - cm heterogeneous uterine mass and a 1.9-cm hypoenhancing lesion in the pancreatic head. Pelvic MRI findings suggested uLMS. Endoscopic ultrasound-guided biopsy confirmed the pancreatic lesion as metastatic leiomyosarcoma. No other sites of metastatic disease were found. Due to her extensive comorbidities and limited performance status, the patient ultimately elected for hospice care after being thoroughly counseled on her treatment options and multidisciplinary consultation.

Conclusion: This case illustrates a rare instance of isolated pancreatic metastasis from primary uLMS, a presentation that can mimic primary pancreatic cancer. It emphasizes the need for a broad differential diagnosis, histologic confirmation, and individualized treatment planning in medically complex patients.

子宫平滑肌肉瘤胰腺少转移1例。
背景:子宫平滑肌肉瘤(uLMS)是一种罕见的侵袭性子宫恶性肿瘤,预后差,因其早期血液扩散,典型的肺和肝脏,复发率高。胰腺转移异常罕见,孤立累及胰腺更是罕见。病例:一名81岁的患者在未被目击的跌倒和新的神经症状后入院,后来被诊断为小脑卒中。尿潴留的盆腔成像显示9.9 × 15.1 × 18.8 cm的异质子宫肿块和1.9 cm的胰头低增强病变。骨盆MRI结果提示uLMS。内镜下超声引导活检证实胰腺病变为转移性平滑肌肉瘤。未发现其他部位的转移性疾病。由于她有广泛的合并症和有限的表现状况,病人在接受了全面的治疗方案和多学科咨询后,最终选择了临终关怀。结论:本病例为罕见的原发性uLMS孤立性胰腺转移病例,其表现与原发性胰腺癌相似。它强调需要广泛的鉴别诊断,组织学确认,和个性化的治疗计划在医学复杂的病人。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
11
审稿时长
16 weeks
期刊介绍: Case Reports in Oncological Medicine is a peer-reviewed, Open Access journal that publishes case reports and case series related to breast cancer, lung cancer, gastrointestinal cancer, skin cancer, head and neck cancer, paediatric oncology, neurooncology as well as genitourinary cancer.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书