• 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

了解胆总管畸形。

Understanding choledochal malformation.

机构信息

Department of Paediatric Surgery, King's College Hospital, Denmark Hill, London SE5 9RS, UK.

出版信息

Arch Dis Child. 2012 Jan;97(1):69-72. doi: 10.1136/adc.2010.195974. Epub 2011 Mar 27.

DOI:10.1136/adc.2010.195974
PMID:21444296
Abstract

Choledochal malformations (also known as choledochal cysts) may be characterised as an abnormal dilatation of the biliary tract, in the absence of any acute obstruction. Most appear to be of congenital origin probably related to distal bile duct stenosis, and almost 15% can now be detected antenatally. Excision and biliary reconstruction using a Roux loop as an open operation is still the standard to compare to. This article discusses recent advances in the understanding of their aetiology and classification together with the place of newer modalites of surgical treatment such as laparoscopic excision and biliary reconstruction. Although these are definitely feasible and safe, care should be taken before dispensing with standard open techniques which have minimal complications and proven long-term benefit.

摘要

胆总管畸形(也称为胆总管囊肿)可能表现为胆道的异常扩张,不存在任何急性梗阻。大多数似乎是先天性的,可能与远端胆管狭窄有关,现在近 15%的病例可以在产前检测到。切除和使用 Roux 袢进行胆肠重建仍然是作为标准术式来进行比较。本文讨论了对其病因和分类的最新认识,以及腹腔镜切除和胆肠重建等新的手术治疗方式的应用。虽然这些方法肯定是可行和安全的,但在摒弃具有最小并发症和长期受益的标准开放技术之前,应该谨慎行事。

相似文献

1
Understanding choledochal malformation.了解胆总管畸形。
Arch Dis Child. 2012 Jan;97(1):69-72. doi: 10.1136/adc.2010.195974. Epub 2011 Mar 27.
2
Controversies in choledochal malformation.
S Afr Med J. 2014 Nov;104(11 Pt 2):816-9.
3
Controversies in choledochal malformation.胆总管畸形的争议
S Afr Med J. 2014 Oct 24;104(11):816-819. doi: 10.7196/samj.8633.
4
Choledochal malformations: global research, scientific advances and key controversies.胆管畸形:全球研究、科学进展与关键争议
Pediatr Surg Int. 2019 Mar;35(3):273-282. doi: 10.1007/s00383-018-4392-4. Epub 2018 Nov 7.
5
[Congenital dilatation of the common bile duct (congenital choledochal cyst)].[先天性胆总管扩张症(先天性胆管囊肿)]
Srp Arh Celok Lek. 2001 May-Jun;129 Suppl 1:47-50.
6
[Development of intrahepatic cholelithiasis long after primary excision of choledochal cysts].[胆总管囊肿初次切除术后多年发生肝内胆管结石]
Nihon Geka Gakkai Zasshi. 1996 Aug;97(8):606-10.
7
[Congenital cystic disease of the biliary system in adults].[成人先天性胆道系统囊性疾病]
Rev Med Chir Soc Med Nat Iasi. 2003 Oct-Dec;107(4):817-21.
8
[Choledochal cyst as a complex malformation of the intra and extrahepatic bile ducts].[胆总管囊肿作为肝内和肝外胆管的复杂畸形]
Chirurgia (Bucur). 2005 Jan-Feb;100(1):63-8.
9
Congenital stenosis of the intrahepatic bile duct associated with choledochal cysts.先天性肝内胆管狭窄合并胆总管囊肿
J Am Coll Surg. 1995 Nov;181(5):426-30.
10
[Diagnosis and treatment of congenital biliary duct cyst: twenty-year experience].先天性胆管囊肿的诊断与治疗:二十年经验
Zhonghua Wai Ke Za Zhi. 2001 Dec;39(12):915-7.

引用本文的文献

1
Pancreatic fistula and bleeding following choledochal cyst excision: Experience of two decades.胆总管囊肿切除术后的胰瘘和出血:二十年经验
Turk J Surg. 2024 Jun 28;40(2):104-110. doi: 10.47717/turkjsurg.2024.6354. eCollection 2024 Jun.
2
Biliary Reconstruction with Hepaticoduodenostomy Versus Hepaticojejunostomy After Choledochal Cyst Resection: A Narrative Review.胆总管囊肿切除术后肝十二指肠吻合术与肝空肠吻合术的胆道重建:一项叙述性综述
J Clin Med. 2024 Oct 31;13(21):6556. doi: 10.3390/jcm13216556.
3
Construction of nomogram based on clinical factors for the risk prediction of postoperative complications in children with choledochal cyst.
基于临床因素构建预测胆总管囊肿患儿术后并发症风险的列线图。
Front Pediatr. 2024 Aug 7;12:1372514. doi: 10.3389/fped.2024.1372514. eCollection 2024.
4
Long-term outcome for children undergoing open hepatico-jejunostomy for choledochal malformations: a 43-year single-center experience.开腹肝肠吻合术治疗先天性胆总管囊肿患儿的长期疗效:43 年单中心经验
Pediatr Surg Int. 2024 Jan 19;40(1):36. doi: 10.1007/s00383-023-05622-8.
5
Prevalence of Pancreato-Biliary Maljunction in Children with Choledochal Cyst - A Prospective Observational Study.胆总管囊肿患儿胰胆管合流异常的患病率——一项前瞻性观察研究
J Indian Assoc Pediatr Surg. 2023 Mar-Apr;28(2):137-143. doi: 10.4103/jiaps.jiaps_104_22. Epub 2022 Nov 30.
6
Pathogenesis of Choledochal Cyst: Insights from Genomics and Transcriptomics.先天性胆总管囊肿的发病机制:从基因组学和转录组学角度的新见解。
Genes (Basel). 2022 Jun 8;13(6):1030. doi: 10.3390/genes13061030.
7
Molecular Characteristics of Choledochal Cysts in Children: Transcriptome Sequencing.儿童胆总管囊肿的分子特征:转录组测序
Front Genet. 2021 Aug 3;12:709340. doi: 10.3389/fgene.2021.709340. eCollection 2021.
8
Current Concepts of Biliary Atresia and Matrix Metalloproteinase-7: A Review of Literature.胆道闭锁与基质金属蛋白酶-7的当前概念:文献综述
Front Med (Lausanne). 2020 Dec 21;7:617261. doi: 10.3389/fmed.2020.617261. eCollection 2020.
9
Laparoscopic management of choledochal cyst in children: Lessons learnt from low-middle income countries.儿童胆总管囊肿的腹腔镜治疗:从中低收入国家汲取的经验教训
J Minim Access Surg. 2021 Jul-Sep;17(3):279-286. doi: 10.4103/jmas.JMAS_114_20.
10
Acquired choledochal cyst following intraabdominal tumor surgical excision: A case report.腹腔内肿瘤手术切除后获得性胆总管囊肿:一例报告。
Ann Med Surg (Lond). 2020 Aug 7;57:270-273. doi: 10.1016/j.amsu.2020.08.001. eCollection 2020 Sep.