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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.

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/11768508/925060e29e3f/rjaf029f1.jpg

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