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精索去分化脂肪肉瘤:一例报告并文献复习

Dedifferentiated Liposarcoma of the Spermatic Cord: A Case Report and Review of the Literature.

作者信息

Matsui Yuki, Yanagida Wahei, Kishi Hirotaka, Morita Jun, Fukagai Takashi

机构信息

Department of Urology, Showa University School of Medicine, Tokyo, JPN.

出版信息

Cureus. 2025 Mar 8;17(3):e80264. doi: 10.7759/cureus.80264. eCollection 2025 Mar.

DOI:10.7759/cureus.80264
PMID:40196059
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11975456/
Abstract

Spermatic cord liposarcomas are rare malignant neoplasms with no established level-one evidence-based treatment guidelines. Well-differentiated liposarcomas (WDL) lack metastatic potential but can transform into dedifferentiated liposarcomas (DDL), which are more aggressive. Due to the rarity of these tumors, treatment recommendations are primarily based on retrospective studies and extrapolated data from extremity sarcomas. We report a case of a DDL managed with radical orchiectomy and en bloc resection, along with a literature review on spermatic cord liposarcomas, focusing on imaging, histopathology, and treatment strategies. Imaging techniques, such as magnetic resonance imaging (MRI) and computed tomography (CT), aid in tumor characterization, while histopathological examination remains the gold standard for diagnosis. Surgical management prioritizes R0 resection, as incomplete excision is associated with high recurrence rates. The role of adjuvant therapy remains controversial, with limited evidence supporting its routine use. In our case, complete resection with negative margins was achieved, and clinical follow-up was chosen over adjuvant treatment. Given the aggressive nature of high-grade liposarcomas and their tendency for local recurrence, wide surgical excision with negative margins remains the primary treatment. The role of adjuvant chemotherapy and radiotherapy is unclear and may be considered in high-risk cases. Further research is needed to establish standardized treatment protocols.

摘要

精索脂肪肉瘤是罕见的恶性肿瘤,目前尚无一级循证医学治疗指南。高分化脂肪肉瘤(WDL)无转移潜能,但可转变为侵袭性更强的去分化脂肪肉瘤(DDL)。由于这些肿瘤罕见,治疗建议主要基于回顾性研究以及从肢体肉瘤外推的数据。我们报告一例通过根治性睾丸切除术和整块切除治疗的DDL病例,并对精索脂肪肉瘤进行文献综述,重点关注影像学、组织病理学和治疗策略。磁共振成像(MRI)和计算机断层扫描(CT)等成像技术有助于肿瘤特征的判定,而组织病理学检查仍是诊断的金标准。手术治疗优先考虑R0切除,因为不完全切除与高复发率相关。辅助治疗的作用仍存在争议,支持其常规使用的证据有限。在我们的病例中,实现了切缘阴性的完整切除,选择临床随访而非辅助治疗。鉴于高级别脂肪肉瘤的侵袭性及其局部复发倾向,切缘阴性的广泛手术切除仍是主要治疗方法。辅助化疗和放疗的作用尚不清楚,高危病例可考虑使用。需要进一步研究以建立标准化治疗方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b251/11975456/471c9cacd6b7/cureus-0017-00000080264-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b251/11975456/35c128349862/cureus-0017-00000080264-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b251/11975456/6d7bb3dc4ebb/cureus-0017-00000080264-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b251/11975456/64695101d5be/cureus-0017-00000080264-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b251/11975456/471c9cacd6b7/cureus-0017-00000080264-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b251/11975456/35c128349862/cureus-0017-00000080264-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b251/11975456/6d7bb3dc4ebb/cureus-0017-00000080264-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b251/11975456/64695101d5be/cureus-0017-00000080264-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b251/11975456/471c9cacd6b7/cureus-0017-00000080264-i04.jpg

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本文引用的文献

1
Integrated exome and RNA sequencing of dedifferentiated liposarcoma.去分化脂肪肉瘤的外显子组和 RNA 测序整合分析。
Nat Commun. 2019 Dec 12;10(1):5683. doi: 10.1038/s41467-019-13286-z.
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[A Case of Dedifferentiated Liposarcoma of the Spermatic Cord].[精索去分化脂肪肉瘤一例]
Hinyokika Kiyo. 2019 Oct;65(10):429-434. doi: 10.14989/ActaUrolJap_65_10_429.
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Liposarcoma in the Inguinal Canal: Challenges in Preoperative Diagnosis and Importance of Routine Pathological Examination of "Hernia Sacs".腹股沟管脂肪肉瘤:术前诊断的挑战及“疝囊”常规病理检查的重要性
Case Rep Pathol. 2018 Sep 6;2018:5929626. doi: 10.1155/2018/5929626. eCollection 2018.
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Current management of liposarcoma of the spermatic cord: A case report and review of the literature.精索脂肪肉瘤的当前管理:一例病例报告及文献综述。
Mol Clin Oncol. 2017 Mar;6(3):438-440. doi: 10.3892/mco.2017.1157. Epub 2017 Feb 6.
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Dedifferentiated liposarcoma of the spermatic cord: a series of 42 cases.精索去分化脂肪肉瘤:系列病例 42 例。
Am J Surg Pathol. 2015 Sep;39(9):1219-25. doi: 10.1097/PAS.0000000000000426.
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Primary spermatic cord tumors: disease characteristics, prognostic factors, and treatment outcomes.原发性精索肿瘤:疾病特征、预后因素及治疗结果
Urol Oncol. 2014 Jan;32(1):52.e19-25. doi: 10.1016/j.urolonc.2013.08.009. Epub 2013 Nov 13.
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Ther Adv Urol. 2012 Dec;4(6):325-34. doi: 10.1177/1756287212447839.
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Chirurgia (Bucur). 2010 Mar-Apr;105(2):257-66.
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Diagnosis and management of lipomatous tumors.脂肪瘤性肿瘤的诊断与管理
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10
Adult genitourinary sarcoma: the 25-year Memorial Sloan-Kettering experience.成人泌尿生殖系统肉瘤:纪念斯隆-凯特琳癌症中心25年的经验
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