• 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

偶然发现伴有或不伴有腹膜假黏液瘤的阑尾黏液性上皮肿瘤:基于现有证据的诊断和治疗算法。

Incidentally found mucinous epithelial tumors of the appendix with or without pseudomyxoma peritonei: diagnostic and therapeutic algorithms based on current evidence.

机构信息

Department ofGI Surgery, Ghent University Hospital, Ghent, Belgium.

Department of Digestive Oncology, Ghent University Hospital, Ghent, Belgium.

出版信息

Acta Chir Belg. 2021 Aug;121(4):225-234. doi: 10.1080/00015458.2021.1894734. Epub 2021 May 31.

DOI:10.1080/00015458.2021.1894734
PMID:33904809
Abstract

Mucinous appendiceal tumors with or without the pseudomyxoma peritonei (PMP) syndrome are rare, but often present as an incidental finding. The confusing histology and lack of large prospective trials result in a considerable diagnostic and therapeutic challenge in these patients. We propose treatment algorithms in patients with incidentally found mucinous epithelial appendiceal tumors, with or without PMP, based on the currently available evidence. The therapeutic approach should take into account the histology and grade of the primary appendix tumor, as well as those of the associated peritoneal disease.

摘要

黏液性阑尾肿瘤伴或不伴腹膜假黏液瘤(PMP)综合征较为罕见,但常为偶然发现。由于其组织学表现复杂,且缺乏大型前瞻性临床试验,这些患者的诊断和治疗极具挑战性。我们根据现有证据,为偶然发现的黏液性上皮性阑尾肿瘤患者(伴或不伴 PMP)提出了治疗方案。治疗方法应考虑阑尾原发肿瘤的组织学和分级,以及相关腹膜疾病的组织学和分级。

相似文献

1
Incidentally found mucinous epithelial tumors of the appendix with or without pseudomyxoma peritonei: diagnostic and therapeutic algorithms based on current evidence.偶然发现伴有或不伴有腹膜假黏液瘤的阑尾黏液性上皮肿瘤:基于现有证据的诊断和治疗算法。
Acta Chir Belg. 2021 Aug;121(4):225-234. doi: 10.1080/00015458.2021.1894734. Epub 2021 May 31.
2
[Incidental finding of appendiceal mucinous neoplasms].阑尾黏液性肿瘤的偶然发现
Chirurgie (Heidelb). 2023 Oct;94(10):832-839. doi: 10.1007/s00104-023-01910-0. Epub 2023 Jun 28.
3
Appendiceal pseudomyxoma peritonei in a pregnant woman.一名孕妇的腹膜假黏液瘤
Saudi Med J. 2010 May;31(5):572-4.
4
A case of Pseudomyxoma Peritonei of an unexpected origin.一例来源不明的假性黏液瘤腹膜病。
Diagn Pathol. 2021 Dec 20;16(1):119. doi: 10.1186/s13000-021-01179-z.
5
Appendiceal tumours and pseudomyxoma peritonei: Literature review with PSOGI/EURACAN clinical practice guidelines for diagnosis and treatment.阑尾肿瘤和腹膜假黏液瘤:文献综述及 PSOGI/EURACAN 诊断和治疗临床实践指南。
Eur J Surg Oncol. 2021 Jan;47(1):11-35. doi: 10.1016/j.ejso.2020.02.012. Epub 2020 Feb 28.
6
Appendiceal mucocele and pseudomyxoma peritonei; the clinical boundaries of a subtle disease.阑尾黏液囊肿与腹膜假黏液瘤;一种隐匿性疾病的临床界限
Am J Case Rep. 2014 Aug 27;15:355-60. doi: 10.12659/AJCR.890837.
7
Pseudomyxoma peritonei induced by low-grade appendiceal mucinous neoplasm accompanied by rectal cancer: a case report and literature review.低度阑尾黏液性肿瘤伴直肠癌所致腹膜假黏液瘤:1例报告及文献复习
BMC Surg. 2019 Apr 25;19(1):42. doi: 10.1186/s12893-019-0508-6.
8
Mode of Presentation in 1070 Patients With Perforated Epithelial Appendiceal Tumors, Predominantly with Pseudomyxoma Peritonei.1070 例穿孔性上皮性阑尾肿瘤患者的临床表现,主要为腹膜假黏液瘤。
Dis Colon Rectum. 2020 Sep;63(9):1257-1264. doi: 10.1097/DCR.0000000000001682.
9
Appendiceal mucinous neoplasms: controversial issues.阑尾黏液性肿瘤:争议问题。
Arch Pathol Lab Med. 2010 Jun;134(6):864-70. doi: 10.5858/134.6.864.
10
Strategies for Preventing Pseudomyxoma Peritonei After Resection of a Mucinous Neoplasm of the Appendix.阑尾黏液性肿瘤切除术后预防腹膜假黏液瘤的策略。
Anticancer Res. 2015 Sep;35(9):4943-7.

引用本文的文献

1
Diagnostic difficulties in the differentiation between an ovarian metastatic low‑grade appendiceal mucinous neoplasm and primary ovarian mucinous cancer: A case report and literature review.卵巢转移性低级别阑尾黏液性肿瘤与原发性卵巢黏液癌鉴别诊断的困难:一例报告及文献复习
Oncol Lett. 2024 Aug 16;28(5):500. doi: 10.3892/ol.2024.14633. eCollection 2024 Nov.