Deep Venous Thrombosis as the Sentinel Event Unmasking a Uterine Leiomyosarcoma in a Postmenopausal Woman: A Case Report and Review of the Literature.

IF 0.7 Q4 ONCOLOGY
Case Reports in Oncology Pub Date : 2025-09-02 eCollection Date: 2025-01-01 DOI:10.1159/000548265
Omran Janoud, Ibrahim Abd Alrahem Jaber, Kinan Jafar, Alaa Jlailati, Ahmad Al-Bitar, Souheb Al-Mahasna
{"title":"Deep Venous Thrombosis as the Sentinel Event Unmasking a Uterine Leiomyosarcoma in a Postmenopausal Woman: A Case Report and Review of the Literature.","authors":"Omran Janoud, Ibrahim Abd Alrahem Jaber, Kinan Jafar, Alaa Jlailati, Ahmad Al-Bitar, Souheb Al-Mahasna","doi":"10.1159/000548265","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Uterine tumors are classified as benign or malignant, with leiomyomas being the most common benign type and leiomyosarcomas (LMSs) being a rare but aggressive form of uterine sarcoma. The clinical similarity between these two tumor types often makes preoperative differentiation challenging, necessitating surgery for a definitive diagnosis. LMSs are highly aggressive with a poor prognosis. We present the case of a 60-year-old woman whose uterine LMS was initially diagnosed as a benign myoma, with deep venous thrombosis (DVT) serving as an atypical presenting sign of her underlying malignancy.</p><p><strong>Case presentation: </strong>A 60-year-old postmenopausal woman presented with a large, progressively enlarging abdominal mass, which had been identified 5 years prior as a probable leiomyoma. She initially declined surgery but was readmitted 1 month later with a DVT in her left leg, which was attributed to the compressive effect of the large pelvic mass. The patient underwent a total abdominal hysterectomy. Histopathological and immunohistochemical analysis of the 21-cm uterine tumor confirmed a high-grade LMS. Subsequent staging scans revealed Stage IVB metastatic disease in her lungs, liver, and bones. The patient was transitioned to palliative care and passed away 6 weeks after her surgery.</p><p><strong>Conclusion: </strong>Uterine LMSs can deceptively mimic benign leiomyomas, which may lead to significant diagnostic delays and contribute to poor outcomes. This case highlights that an atypical presentation, such as an idiopathic deep vein thrombosis, should heighten clinical suspicion for an underlying pelvic malignancy, even in the absence of typical gynecological symptoms. Accurate and timely diagnosis is critical and ultimately depends on definitive histopathological evaluation, underscoring the highly aggressive nature and significant mortality associated with this rare cancer.</p>","PeriodicalId":9625,"journal":{"name":"Case Reports in Oncology","volume":"18 1","pages":"1297-1306"},"PeriodicalIF":0.7000,"publicationDate":"2025-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12503845/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Case Reports in Oncology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1159/000548265","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q4","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction: Uterine tumors are classified as benign or malignant, with leiomyomas being the most common benign type and leiomyosarcomas (LMSs) being a rare but aggressive form of uterine sarcoma. The clinical similarity between these two tumor types often makes preoperative differentiation challenging, necessitating surgery for a definitive diagnosis. LMSs are highly aggressive with a poor prognosis. We present the case of a 60-year-old woman whose uterine LMS was initially diagnosed as a benign myoma, with deep venous thrombosis (DVT) serving as an atypical presenting sign of her underlying malignancy.

Case presentation: A 60-year-old postmenopausal woman presented with a large, progressively enlarging abdominal mass, which had been identified 5 years prior as a probable leiomyoma. She initially declined surgery but was readmitted 1 month later with a DVT in her left leg, which was attributed to the compressive effect of the large pelvic mass. The patient underwent a total abdominal hysterectomy. Histopathological and immunohistochemical analysis of the 21-cm uterine tumor confirmed a high-grade LMS. Subsequent staging scans revealed Stage IVB metastatic disease in her lungs, liver, and bones. The patient was transitioned to palliative care and passed away 6 weeks after her surgery.

Conclusion: Uterine LMSs can deceptively mimic benign leiomyomas, which may lead to significant diagnostic delays and contribute to poor outcomes. This case highlights that an atypical presentation, such as an idiopathic deep vein thrombosis, should heighten clinical suspicion for an underlying pelvic malignancy, even in the absence of typical gynecological symptoms. Accurate and timely diagnosis is critical and ultimately depends on definitive histopathological evaluation, underscoring the highly aggressive nature and significant mortality associated with this rare cancer.

深静脉血栓形成作为揭示绝经后妇女子宫平滑肌肉瘤的前哨事件:一例报告和文献回顾。
子宫肿瘤分为良性和恶性,其中平滑肌瘤是最常见的良性类型,而平滑肌肉瘤(lms)是一种罕见但具有侵袭性的子宫肉瘤。这两种肿瘤类型的临床相似性往往使术前鉴别具有挑战性,需要手术进行明确诊断。lms侵袭性强,预后差。我们报告一位60岁的女性,她的子宫LMS最初被诊断为良性肌瘤,深静脉血栓形成(DVT)是她潜在恶性肿瘤的不典型表现。病例介绍:一名60岁绝经后妇女,5年前被诊断为可能的平滑肌瘤,腹部肿块逐渐增大。患者最初拒绝手术,但1个月后因左腿深静脉血栓再次入院,这是由于大盆腔肿块的压缩作用。患者接受了腹部全子宫切除术。21厘米子宫肿瘤的组织病理学和免疫组织化学分析证实为高级别LMS。随后的分期扫描显示她的肺、肝和骨骼有IVB期转移性疾病。患者被转移到姑息治疗,并在手术后6周去世。结论:子宫lms可伪装成良性平滑肌瘤,可能导致诊断延误和预后不良。本病例强调了一个不典型的表现,如特发性深静脉血栓形成,应提高临床怀疑潜在的盆腔恶性肿瘤,即使没有典型的妇科症状。准确和及时的诊断至关重要,最终取决于明确的组织病理学评估,强调了这种罕见癌症的高度侵袭性和显著死亡率。
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
CiteScore
1.40
自引率
12.50%
发文量
151
审稿时长
7 weeks
×
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