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表现为幽门梗阻的胆囊胃瘘——布韦雷氏综合征:一例报告

Cholecystogastric fistula presenting as pyloric obstruction - a Bouveret's syndrome: A case report.

作者信息

Yang Yi, Zhong Ding-Fu

机构信息

Department of Gastroenterology, Affiliated Jinhua Hospital of Wenzhou Medical University, Jinhua People's Hospital, Jinhua 321000, Zhejiang Province, China.

出版信息

World J Gastrointest Endosc. 2025 Jan 16;17(1):101534. doi: 10.4253/wjge.v17.i1.101534.

Abstract

BACKGROUND

Bouveret's syndrome is a rare (1%-4%) form of cholelithiasis characterized by gastric outlet obstruction. It presents mainly in elderly women with nausea, vomiting, and abdominal pain. On physical examination, common findings include dehydration signs such as tachycardia, decreased urine output, abdominal discomfort, and distention. Diagnosis relies on computed tomography (CT) and magnetic resonance imaging, with Rigler's triad (pneumobilia, ectopic gallstone, gastric distension) being highly specific. This report aims to improve understanding of Bouveret's syndrome and inform better management and treatment strategies.

CASE SUMMARY

A 60-year-old male patient presented with a three-day history of nausea, vomiting, upper abdominal pain, and loss of appetite. An upright abdominal X-ray revealed a gas shadow in the intrahepatic and extrahepatic bile ducts. Endoscopy revealed a brown and black stone measuring approximately 3030 mm in diameter in the gastric pylorus, incompletely obstructing the gastric outlet. The diagnosis of Bouveret's syndrome was accurately confirmed an abdominal CT scan. Endoscopic removal of the stone was successful, owing to the stone being fragmented and extracted in pieces using a crushing basket. Three weeks later, laparoscopy was attempted but failed because of severe tissue adhesions. Consequently, the procedure was converted to a laparotomy, and fistula repair and cholecystectomy were performed. He returned to the outpatient clinic for follow-up, and no further concerns were noted.

CONCLUSION

This case highlights the importance of timely diagnosis and adaptable endoscopic and surgical approaches for effectively managing Bouveret's syndrome.

摘要

背景

布韦雷氏综合征是一种罕见(1%-4%)的胆石症形式,其特征为胃出口梗阻。它主要发生于老年女性,表现为恶心、呕吐和腹痛。体格检查时,常见体征包括脱水迹象,如心动过速、尿量减少、腹部不适和腹胀。诊断依赖于计算机断层扫描(CT)和磁共振成像,里格勒三联征(气肿性胆囊炎、异位胆结石、胃扩张)具有高度特异性。本报告旨在增进对布韦雷氏综合征的了解,并为更好的管理和治疗策略提供依据。

病例摘要

一名60岁男性患者出现恶心、呕吐、上腹部疼痛和食欲不振三天的症状。立位腹部X线检查显示肝内和肝外胆管有气体阴影。内镜检查发现胃幽门处有一块直径约30×30毫米的棕黑色结石,不完全阻塞胃出口。腹部CT扫描准确确诊为布韦雷氏综合征。由于使用碎石篮将结石破碎并逐块取出,内镜下成功取出结石。三周后,尝试进行腹腔镜检查,但因严重的组织粘连而失败。因此,手术改为剖腹手术,并进行了瘘管修复和胆囊切除术。他返回门诊进行随访,未发现进一步问题。

结论

本病例强调了及时诊断以及灵活采用内镜和手术方法对有效管理布韦雷氏综合征的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/add8/11752466/3df1e8722491/101534-g001.jpg

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