• 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

原发性口腔平滑肌肉瘤:系统评价与更新。

Primary oral leiomyosarcoma: A systematic review and update.

机构信息

Department of Oral Medicine, School of Dental Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.

出版信息

J Oral Pathol Med. 2019 Oct;48(9):780-787. doi: 10.1111/jop.12858. Epub 2019 Apr 25.

DOI:10.1111/jop.12858
PMID:30958581
Abstract

The aim of this systematic review was to address the clinicopathologic inconsistencies noted with primary oral leiomyosarcoma in the literature by amassing the available data published into a comprehensive analysis. Eligibility criteria included publications of cases with dedicated immunohistochemical work-up along with radiographs to evaluate location. Based on these criteria, the systematic review compiled 29 cases. Four primary location sites were identified in the reported cases: soft tissue presentation only, soft tissue with bony involvement, bony involvement only, and bony involvement with a soft tissue component. The majority of primary oral leiomyosarcoma cases reviewed showed a soft tissue predilection, which is in contrast to prior reports of jawbones being the most common site. In addition, there was an improved 5-year survival rate for primary oral leiomyosarcoma limited to the oral cavity and gnathic bones without extension into paranasal sinuses.

摘要

本系统评价的目的是通过汇集已发表的可用数据进行综合分析,解决文献中原发性口腔平滑肌肉瘤的临床病理不一致性。纳入标准包括具有专门免疫组织化学检查和评估位置的放射学检查的病例报告。基于这些标准,系统评价共纳入了 29 例病例。在报告的病例中确定了四个主要部位:仅软组织表现、软组织伴骨累及、仅骨累及和骨累及伴软组织成分。回顾的大多数原发性口腔平滑肌肉瘤病例表现出软组织倾向,这与先前报道的颌骨是最常见部位的观点相反。此外,原发性口腔平滑肌肉瘤仅限于口腔和颌骨且不向鼻窦扩展的患者,5 年生存率有所提高。

相似文献

1
Primary oral leiomyosarcoma: A systematic review and update.原发性口腔平滑肌肉瘤:系统评价与更新。
J Oral Pathol Med. 2019 Oct;48(9):780-787. doi: 10.1111/jop.12858. Epub 2019 Apr 25.
2
Primary oral leiomyosarcoma: a retrospective clinical analysis of 20 cases.原发性口腔平滑肌肉瘤:20 例回顾性临床分析。
Oral Dis. 2010 Mar;16(2):198-203. doi: 10.1111/j.1601-0825.2009.01635.x.
3
Leiomyosarcomas of the oral tissues: clinicopathologic analysis of 50 cases.口腔组织平滑肌肉瘤:50例临床病理分析
J Oral Maxillofac Surg. 2005 Oct;63(10):1461-77. doi: 10.1016/j.joms.2005.06.018.
4
[Bone metastasis of leiomyosarcoma. Apropos of a case].[平滑肌肉瘤的骨转移。附1例报告]
Rev Chir Orthop Reparatrice Appar Mot. 1995;81(4):338-43.
5
Reassessment and clinicopathological prognostic factors of malignant fibrous histiocytoma of soft parts.软组织恶性纤维组织细胞瘤的重新评估及临床病理预后因素
Pathol Int. 2002 Sep;52(9):595-606. doi: 10.1046/j.1440-1827.2002.01399.x.
6
Pleomorphic leiomyosarcoma: clinicopathologic and immunohistochemical study with special emphasis on its distinction from ordinary leiomyosarcoma and malignant fibrous histiocytoma.多形性平滑肌肉瘤:临床病理及免疫组化研究,特别强调其与普通平滑肌肉瘤及恶性纤维组织细胞瘤的鉴别
Am J Surg Pathol. 2001 Aug;25(8):1030-8. doi: 10.1097/00000478-200108000-00007.
7
Leiomyosarcoma of the nasal cavity. Case report and literature review.鼻腔平滑肌肉瘤。病例报告及文献综述。
ORL J Otorhinolaryngol Relat Spec. 1996 Mar-Apr;58(2):115-20. doi: 10.1159/000276810.
8
Pediatric oral leiomyosarcoma: rare case report.小儿口腔平滑肌肉瘤:罕见病例报告。
J Cancer Res Ther. 2012 Apr-Jun;8(2):282-5. doi: 10.4103/0973-1482.98990.
9
Primary leiomyosarcoma of bone: a clinicopathologic, immunohistochemical, and ultrastructural study of 33 patients and a literature review.骨原发性平滑肌肉瘤:33例患者的临床病理、免疫组织化学及超微结构研究并文献复习
Am J Surg Pathol. 1997 Nov;21(11):1281-94. doi: 10.1097/00000478-199711000-00003.
10
Primary gingival leiomyosarcoma. A clinicopathological study of 1 case with prolonged survival.原发性牙龈平滑肌肉瘤。1例长期存活患者的临床病理研究
J Clin Periodontol. 2002 Feb;29(2):182-7. doi: 10.1034/j.1600-051x.2002.290214.x.

引用本文的文献

1
Primary leiomyosarcoma of bone: a clinicopathologic and immunohistochemical study of 142 cases.骨原发性平滑肌肉瘤:142例临床病理及免疫组织化学研究
Pathologica. 2025 Jun;117(3):288-295. doi: 10.32074/1591-951X-N1251.
2
Trial for diagnosis - A case report of recurrent oral leiomyosarcoma.诊断性试验——复发性口腔平滑肌肉瘤病例报告
Indian J Otolaryngol Head Neck Surg. 2025 Mar;77(3):1646-1650. doi: 10.1007/s12070-025-05358-y. Epub 2025 Jan 22.
3
Primary oral leiomyosarcoma of the maxillary bone and sinus: case report and up-to-date review of literature.
上颌骨和鼻窦原发性口腔平滑肌肉瘤:病例报告及文献最新综述
Braz J Otorhinolaryngol. 2022 Nov-Dec;88 Suppl 4(Suppl 4):S205-S211. doi: 10.1016/j.bjorl.2021.07.013. Epub 2021 Oct 17.
4
Leiomyoma and Leiomyosarcoma (Primary and Metastatic) of the Oral and Maxillofacial Region: A Clinicopathological and Immunohistochemical Study of 27 Cases.口腔颌面部平滑肌瘤和平滑肌肉瘤(原发性和转移性):27 例临床病理和免疫组织化学研究。
Head Neck Pathol. 2022 Mar;16(1):294-303. doi: 10.1007/s12105-021-01336-2. Epub 2021 Jun 9.
5
Leiomyosarcoma of the jaw: case series.颌骨平滑肌肉瘤:病例系列
J Korean Assoc Oral Maxillofac Surg. 2020 Aug 31;46(4):275-281. doi: 10.5125/jkaoms.2020.46.4.275.