• 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

胆总管重复畸形合并背侧胰腺发育不全：一个诊断难题及主要治疗转折点

Duplication of the common bile duct associated with dorsal pancreas agenesis: a diagnostic enigma and a major therapeutic turning point.

作者信息

Deflaoui Tarik, Derkaoui Anas, Soussan Haitam, Akil Yassir, Amara Rihab, Guellil Abdelali, Jabi Rachid, Bouziane Mohammed

机构信息

Department of General Surgery, Mohammed VI University Hospital, Oujda, Morocco.

Department of Medicine, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, Mohammed I University, Oujda, Morocco.

出版信息

J Surg Case Rep. 2025 Jan 26;2025(1):rjaf029. doi: 10.1093/jscr/rjaf029. eCollection 2025 Jan.

DOI:10.1093/jscr/rjaf029
PMID:39867985
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11768508/
Abstract

We present a pioneering case of a duplication of the common bile duct associated with agenesis of the dorsal pancreas in a 66-year-old man. After an episode of cholestatic jaundice, radiological investigations revealed complex vascular and biliary anomalies, redefining the therapeutic strategy. Instead of risky surgery, endoscopic biliopancreatic drainage resolved the symptoms. This rare and complex case offers new perspectives for the management of such anomalies, underlining the importance of a personalized, multidisciplinary approach.

摘要

我们报告了一例66岁男性患者的罕见病例，该患者胆总管重复畸形并伴有背侧胰腺发育不全。在出现胆汁淤积性黄疸后，影像学检查发现了复杂的血管和胆道异常，从而重新确定了治疗策略。内镜下胆胰引流术而非风险较大的手术解决了症状。这一罕见且复杂的病例为此类异常情况的处理提供了新的视角，强调了个性化多学科方法的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27be/11768508/623207dad84f/rjaf029f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27be/11768508/925060e29e3f/rjaf029f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27be/11768508/de559a2bfd47/rjaf029f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27be/11768508/623207dad84f/rjaf029f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27be/11768508/925060e29e3f/rjaf029f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27be/11768508/de559a2bfd47/rjaf029f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27be/11768508/623207dad84f/rjaf029f3.jpg

相似文献

1
Duplication of the common bile duct associated with dorsal pancreas agenesis: a diagnostic enigma and a major therapeutic turning point.胆总管重复畸形合并背侧胰腺发育不全：一个诊断难题及主要治疗转折点
J Surg Case Rep. 2025 Jan 26;2025(1):rjaf029. doi: 10.1093/jscr/rjaf029. eCollection 2025 Jan.
2
An unusual variant of type I common bile duct duplication associated with ampullary carcinoma.一种与壶腹癌相关的I型胆总管重复畸形的罕见变异型。
Arch Clin Cases. 2024 Jul 16;11(2):56-60. doi: 10.22551/2024.43.1102.10289. eCollection 2024.
3
Partial agenesis of dorsal pancreas. Report of two cases.背侧胰腺部分发育不全。两例报告。
Int J Surg Case Rep. 2020;77S(Suppl):S17-S20. doi: 10.1016/j.ijscr.2020.10.029. Epub 2020 Oct 10.
4
Dorsal pancreas agenesis, an incidental finding during acute appendicitis diagnosis; A case report.背侧胰腺发育不全，急性阑尾炎诊断时的偶然发现；一例病例报告。
Int J Surg Case Rep. 2023 Aug;109:108567. doi: 10.1016/j.ijscr.2023.108567. Epub 2023 Jul 28.
5
Robotic Biliary Stricturoplasty and Roux-en-Y Hepaticojejunostomy After Hepatic Artery Infusion Pump Injury.机器人胆道狭窄成形术和 Roux-en-Y 肝肠吻合术治疗肝动脉灌注泵损伤。
Ann Surg Oncol. 2024 Jul;31(7):4449-4451. doi: 10.1245/s10434-024-15258-0. Epub 2024 Apr 17.
6
Robotic Klatskin Type 3A Resection with Biliary Reconstruction: Description of Surgical Technique and Outcomes of Initial Series.机器人 Klatskin 型 3A 切除术联合胆道重建：手术技术描述及初步系列结果。
Ann Surg Oncol. 2023 Dec;30(13):8559-8560. doi: 10.1245/s10434-023-14256-y. Epub 2023 Sep 8.
7
A case of dorsal agenesis of pancreas associated with unilateral renal agenesis, unicornuate uterus, and ovarian ectopia: A brief review and learning points.一例胰腺背侧发育不全合并单侧肾缺如、单角子宫和卵巢异位：简要综述及学习要点
Indian J Radiol Imaging. 2020 Jul-Sep;30(3):395-399. doi: 10.4103/ijri.IJRI_165_19. Epub 2020 Oct 15.
8
Dorsal pancreatic agenesis: a case report.背侧胰腺发育不全：一例报告。
Ann Med Surg (Lond). 2023 May 18;85(6):2949-2952. doi: 10.1097/MS9.0000000000000136. eCollection 2023 Jun.
9
Agenesis of dorsal pancreas associated with periampullary pancreaticobiliary type adenocarcinoma.背侧胰腺发育不全伴壶腹周围胰胆管型腺癌。
JOP. 2014 Sep 28;15(5):489-92. doi: 10.6092/1590-8577/2636.
10
Partial agenesis of the dorsal pancreas with features of chronic pancreatitis: A case report.伴有慢性胰腺炎特征的背侧胰腺部分发育不全：病例报告
Radiol Case Rep. 2024 Nov 10;20(1):674-679. doi: 10.1016/j.radcr.2024.10.050. eCollection 2025 Jan.

引用本文的文献

1
Acute pancreatitis revealing adult lymphocytic leukemia in a patient with double cystic duct: a rare case report.双胆囊管患者急性胰腺炎并发成人淋巴细胞白血病：一例罕见病例报告
J Surg Case Rep. 2025 Jul 30;2025(7):rjaf580. doi: 10.1093/jscr/rjaf580. eCollection 2025 Jul.

本文引用的文献

1
Agenesis of the dorsal pancreas and its association with pancreatic tumors.背侧胰腺发育不全及其与胰腺肿瘤的关联。
Pancreas. 2009 May;38(4):367-73. doi: 10.1097/MPA.0b013e318196c401.
2
Role of endoscopic ultrasound in the diagnosis of agenesis of the dorsal pancreas.内镜超声在诊断背侧胰腺发育不全中的作用。
JOP. 2006 Jul 10;7(4):411-6.
3
Double common bile duct: a case report and a review of the Japanese literature.双胆总管：一例病例报告及日本文献综述
Surgery. 2002 Jun;131(6):676-81. doi: 10.1067/msy.2002.124025.
4
Nationwide survey of cases of choledochal cyst. Analysis of coexistent anomalies, complications and surgical treatment in 645 cases.全国胆总管囊肿病例调查。645例并存异常、并发症及手术治疗分析。
Surg Gastroenterol. 1984;3(2):69-73.
5
[A rare anomaly of the bile ducts].[一种罕见的胆管异常]
Ned Tijdschr Geneeskd. 1969 Feb 1;113(5):198-200.
6
Double common bile duct. Case report and review.
Endoscopy. 1986 Jul;18(4):159-61. doi: 10.1055/s-2007-1018360.
7
[A case of duplication of the common bile duct with anomaly of the intrahepatic bile duct].
Nihon Geka Gakkai Zasshi. 1988 Aug;89(8):1296-301.
8
[Rare abnormality of the extrahepatic bile duct and the V. coronaria ventriculi].[肝外胆管及胃冠状静脉的罕见异常]
Chirurg. 1977 Feb;48(2):77-80.