Suppr超能文献

腹腔镜胆囊切除术治疗三胆囊畸形:一例综合病例报告及文献综述

Laparoscopic cholecystectomy for triple gallbladder malformation: A comprehensive case report and literature review.

作者信息

Zhou Shuang-Hao, Li Zhen-Hua, Wei Yao-Chen, Wu Zhi-Yu, Fu Qing-Jiang, Cao Li-Ying, Ma Xiang-Ming

机构信息

Hepatobiliary Surgery, Kailuan General Hospital, Tangshan, Hebei Province, China.

Graduate School, North China University of Science and Technology, Tangshan, Hebei Province, China.

出版信息

Medicine (Baltimore). 2025 Jan 10;104(2):e41190. doi: 10.1097/MD.0000000000041190.

Abstract

RATIONALE

Triple gallbladder is a rare congenital anatomical abnormality because of the incomplete regression of rudimentary bile ducts and is often not found until it is accidentally detected during imaging research.

PATIENT CONCERNS

We report a rare case of triple gallbladder malformation and review the English literature on biliary tract variation caused by gallbladder malformation. The diagnosis, treatment, and postoperative situation of the patients were summarized and analyzed.

DIAGNOSES

The patient was diagnosed with triple gallbladder malformation.

INTERVENTIONS

We conducted laparoscopic cholecystectomy for the patient.

OUTCOMES

We successfully removed all 3 gallbladders by laparoscopic cholecystectomy, and the patient had no postoperative complications such as bleeding or bile leakage and recovered well.

LESSONS

At present, the best treatment for triple gallbladder malformation is to remove all 3 gallbladders by laparoscopic cholecystectomy, which can effectively prevent the occurrence of "postcholecystectomy syndrome" caused by individual gallbladder residue. However, the diagnosis of triple gallbladder is very challenging and often requires a combination of advanced imaging methods. However, sometimes preoperative imaging does not fully reveal biliary tract variation. Therefore, we need to rely on the guidance of evidence-based medicine before surgery and the accurate evaluation of surgical plans to complete the operation without risk.

摘要

理论依据

三胆囊是一种罕见的先天性解剖异常,由于原始胆管不完全退化所致,通常在影像学检查中偶然发现之前不会被察觉。

患者情况

我们报告一例罕见的三胆囊畸形病例,并回顾英文文献中关于胆囊畸形引起的胆道变异情况。总结并分析了患者的诊断、治疗及术后情况。

诊断

该患者被诊断为三胆囊畸形。

干预措施

我们为该患者实施了腹腔镜胆囊切除术。

结果

通过腹腔镜胆囊切除术,我们成功切除了所有3个胆囊,患者术后未出现出血或胆漏等并发症,恢复良好。

经验教训

目前,三胆囊畸形的最佳治疗方法是通过腹腔镜胆囊切除术切除所有3个胆囊,这可有效预防因单个胆囊残留引起的“胆囊切除术后综合征”。然而,三胆囊的诊断极具挑战性,通常需要结合先进的影像学方法。不过,有时术前影像学检查并不能完全揭示胆道变异情况。因此,我们在手术前需要依靠循证医学的指导以及对手术方案的准确评估,以无风险地完成手术。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c919/11730834/e8278e39301e/medi-104-e41190-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验