• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

口腔未分化多形性肉瘤:一种新型基因融合及文献综述

Oral Undifferentiated Pleomorphic Sarcoma: A Novel Gene Fusion and a Comprehensive Literature Review.

作者信息

Della Mura Mario, Sorino Joana, Maiorano Eugenio, Cazzato Gerardo, Colagrande Anna, Manfuso Alfonso, Caporusso Concetta, Copelli Chiara, Cascardi Eliano

机构信息

Section of Molecular Pathology, Department of Precision and Regenerative Medicine and Ionian Area (DiMePRe-J), University of Bari "Aldo Moro", 70124 Bari, Italy.

Maxillofacial Surgery Unit, Interdisciplinary Department of Medicine, University of Bari "Aldo Moro", 70124 Bari, Italy.

出版信息

Genes (Basel). 2025 Jul 17;16(7):830. doi: 10.3390/genes16070830.

DOI:10.3390/genes16070830
PMID:40725486
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12294534/
Abstract

Undifferentiated pleomorphic sarcoma (UPS) is a rare, high-grade soft-tissue sarcoma characterized by a patternless proliferation of bizarre pleomorphic tumor cells lacking identifiable lineage differentiation. Its occurrence in the oral cavity is exceptionally uncommon and poses significant diagnostic challenges due to its morphological overlap with a wide spectrum of other malignancies. : We report a novel case of oral UPS in a 54-year-old woman, characterized by an exceptionally large size and a rapidly progressive clinical course. The diagnostic evaluation included clinical, radiological, histopathological, immunohistochemical, and molecular analyses conducted within a multidisciplinary framework. A comprehensive review of the literature on oral UPS was also performed. : The patient underwent an aggressive demolitive surgical approach due to the extent of the lesion. Molecular analysis revealed a previously unreported gene fusion. The literature review highlighted the rarity of oral UPS, its geographic predilection for Central and East Asia, possible associations with traumatic events, and its heterogeneous clinical and histopathological presentations. : This case underscores the critical importance of a thorough diagnostic workup to ensure the accurate diagnosis and appropriate management of this rare and aggressive tumor. Multidisciplinary evaluation is essential, especially in anatomically complex and diagnostically challenging presentations such as oral UPS.

摘要

未分化多形性肉瘤(UPS)是一种罕见的高级别软组织肉瘤,其特征是形态怪异的多形性肿瘤细胞呈无规律增殖,缺乏可识别的谱系分化。它在口腔中的发生极为罕见,由于其形态与多种其他恶性肿瘤重叠,给诊断带来了重大挑战。我们报告了一例54岁女性口腔UPS的新病例,其特点是肿瘤体积异常大且临床病程进展迅速。诊断评估包括在多学科框架内进行的临床、放射学、组织病理学、免疫组织化学和分子分析。我们还对口腔UPS的文献进行了全面综述。由于病变范围广泛,患者接受了积极的切除性手术。分子分析发现了一种此前未报道的基因融合。文献综述强调了口腔UPS的罕见性、其在中亚和东亚地区的地理倾向性、与创伤事件的可能关联以及其异质性的临床和组织病理学表现。该病例强调了全面诊断检查对于确保准确诊断和妥善处理这种罕见且侵袭性肿瘤的至关重要性。多学科评估至关重要,尤其是在解剖结构复杂且诊断具有挑战性的病例中,如口腔UPS。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/644d/12294534/aa3012123bf8/genes-16-00830-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/644d/12294534/7bd80966be45/genes-16-00830-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/644d/12294534/11f51c6a987d/genes-16-00830-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/644d/12294534/aa3012123bf8/genes-16-00830-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/644d/12294534/7bd80966be45/genes-16-00830-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/644d/12294534/11f51c6a987d/genes-16-00830-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/644d/12294534/aa3012123bf8/genes-16-00830-g003.jpg

相似文献

1
Oral Undifferentiated Pleomorphic Sarcoma: A Novel Gene Fusion and a Comprehensive Literature Review.口腔未分化多形性肉瘤:一种新型基因融合及文献综述
Genes (Basel). 2025 Jul 17;16(7):830. doi: 10.3390/genes16070830.
2
Transoral Videolaryngoscopic Surgery for an Undifferentiated Pleomorphic Sarcoma of the Tongue Base: A Case Report.经口视频喉镜手术治疗舌根未分化多形性肉瘤:病例报告
Reports (MDPI). 2025 Apr 28;8(2):58. doi: 10.3390/reports8020058.
3
Oral Soft Tissue and Jawbone Sarcomas: A Retrospective Clinicopathologic Analysis of 128 Cases from Two Institutions and Comprehensive Literature Review.口腔软组织和颌骨肉瘤:来自两家机构的128例病例回顾性临床病理分析及综合文献综述
Head Neck Pathol. 2025 Jun 17;19(1):74. doi: 10.1007/s12105-025-01811-0.
4
A rare presentation of a cutaneous metastasis from an undifferentiated pleomorphic sarcoma.未分化多形性肉瘤皮肤转移的罕见表现。
J Cancer Res Ther. 2025 Apr 1;21(3):743-745. doi: 10.4103/jcrt.jcrt_1771_24. Epub 2025 Jul 5.
5
The association between the expression of PD-L1 and CMTM6 in undifferentiated pleomorphic sarcoma.未分化多形性肉瘤中 PD-L1 和 CMTM6 的表达之间的关联。
J Cancer Res Clin Oncol. 2021 Jul;147(7):2003-2011. doi: 10.1007/s00432-021-03616-4. Epub 2021 Apr 3.
6
Can a Liquid Biopsy Detect Circulating Tumor DNA With Low-passage Whole-genome Sequencing in Patients With a Sarcoma? A Pilot Evaluation.液体活检能否通过低深度全基因组测序检测肉瘤患者的循环肿瘤DNA?一项初步评估。
Clin Orthop Relat Res. 2025 Jan 1;483(1):39-48. doi: 10.1097/CORR.0000000000003161. Epub 2024 Jun 21.
7
A Review of Intracardiac Mass Cases Encountered Over a Two-Year Period.两年内心脏内肿物病例回顾
Cureus. 2025 Jun 23;17(6):e86619. doi: 10.7759/cureus.86619. eCollection 2025 Jun.
8
Soft tissue sarcoma with MN1 gene fusions: a report of three cases with aggressive clinical behavior.伴有MN1基因融合的软组织肉瘤:三例具有侵袭性临床行为的病例报告。
J Pathol. 2025 Aug;266(4-5):435-446. doi: 10.1002/path.6441. Epub 2025 Jun 12.
9
Prognostic factors and the impact of neoadjuvant chemotherapy on the development of metastasis in patients with undifferentiated pleomorphic sarcoma of soft tissue.软组织未分化多形性肉瘤患者的预后因素及新辅助化疗对转移发生的影响
Int J Clin Oncol. 2025 Jun 11. doi: 10.1007/s10147-025-02807-0.
10
123I-MIBG scintigraphy and 18F-FDG-PET imaging for diagnosing neuroblastoma.用于诊断神经母细胞瘤的123I-间碘苄胍闪烁扫描术和18F-氟代脱氧葡萄糖正电子发射断层显像
Cochrane Database Syst Rev. 2015 Sep 29;2015(9):CD009263. doi: 10.1002/14651858.CD009263.pub2.

本文引用的文献

1
A rare case of undifferentiated pleomorphic sarcoma affecting the mandible - A case report.一例罕见的累及下颌骨的未分化多形性肉瘤——病例报告。
J Oral Maxillofac Pathol. 2024 Jan-Mar;28(1):130-133. doi: 10.4103/jomfp.jomfp_142_23. Epub 2024 Apr 15.
2
Undifferentiated Pleomorphic Sarcoma of the Face.面部未分化多形性肉瘤
Ear Nose Throat J. 2024 May 9:1455613241252890. doi: 10.1177/01455613241252890.
3
SPECC1L: a cytoskeletal protein that regulates embryonic tissue dynamics.SPECC1L:一种调节胚胎组织动力学的细胞骨架蛋白。
Biochem Soc Trans. 2023 Jun 28;51(3):949-958. doi: 10.1042/BST20220461.
4
Undifferentiated pleomorphic sarcoma of the floor of mouth: A rare case.口底未分化多形性肉瘤:1例罕见病例。
J Oral Maxillofac Pathol. 2023 Feb;27(Suppl 1):S33-S37. doi: 10.4103/jomfp.jomfp_107_21. Epub 2023 Feb 4.
5
A Rare Case of Malignant Fibrous Histiocytoma Mimicking Benign Tumour in Maxillofacial Region.一例罕见的颌面部恶性纤维组织细胞瘤误诊为良性肿瘤的病例。
J Maxillofac Oral Surg. 2022 Jun;21(2):701-704. doi: 10.1007/s12663-020-01416-w. Epub 2020 Jul 25.
6
Update from the 5th Edition of the World Health Organization Classification of Head and Neck Tumors: Tumours of the Oral Cavity and Mobile Tongue.从世界卫生组织第五版头颈部肿瘤分类更新:口腔和活动舌肿瘤。
Head Neck Pathol. 2022 Mar;16(1):54-62. doi: 10.1007/s12105-021-01402-9. Epub 2022 Mar 21.
7
Pleomorphic Sarcoma of the Oral Cavity: A Rare Case Entity.口腔多形性肉瘤:一种罕见的病例实体。
J Pharm Bioallied Sci. 2021 Nov;13(Suppl 2):S1747-S1749. doi: 10.4103/jpbs.jpbs_197_21. Epub 2021 Nov 10.
8
A Rare Entity of Undifferentiated Pleomorphic Sarcoma of the Mandible - A Case Report.下颌骨未分化多形性肉瘤的罕见病例——一例报告
Ann Maxillofac Surg. 2021 Jan-Jun;11(1):156-159. doi: 10.4103/ams.ams_334_20. Epub 2021 Jul 24.
9
Primary undifferentiated pleomorphic sarcoma in oral-maxillary area: retrospective study and molecular analysis.口腔颌面部原始未分化多形性肉瘤:回顾性研究和分子分析。
Histol Histopathol. 2021 Aug;36(8):889-898. doi: 10.14670/HH-18-359. Epub 2021 Jul 20.
10
Malignant fibrous histiocytoma of the floor of mouth: a case report and review of the literature.口腔底部恶性纤维组织细胞瘤:一例报告并文献复习
J Stomatol Oral Maxillofac Surg. 2022 Jun;123(3):e106-e111. doi: 10.1016/j.jormas.2021.06.017. Epub 2021 Jul 2.