Laparoscopic management of gallstones in a duplicate gallbladder with double cystic ducts: A case report.

IF 1.7 4区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY
Abuduniyazi Ahunayizhi, Xin-Long Zhang, Qian Chen, Hui Wang, Gang Ding, Sulaiman Akumuo, Xue-Xin Wang, Xiao-Jiao Ruan
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Abstract

Background: Duplicated gallbladder with two completely independent cystic ducts is an exceptionally rare congenital anomaly. This case report documents an example of successful laparoscopic management, adding to the limited literature by highlighting the importance of accurate preoperative imaging and surgical planning.

Case summary: We present the case of a 46-year-old Uyghur woman who was admitted with intermittent right upper abdominal pain accompanied by nausea and vomiting that had persisted for 1 week. Her basic blood test results, including liver function test, were normal. Preoperative ultrasound revealed an abnormal echo in the gallbladder region, suggesting a double gallbladder malformation with one chamber containing multiple stones. Computed tomography and magnetic resonance cholangiopancreatography confirmed a double gallbladder anomaly. The patient subsequently underwent successful laparoscopic cholecystectomy. During the procedure, two gallbladder chambers were identified, with each cystic duct being independently inserted into the common bile duct. Surgery was completed without complications, and postoperative pathology confirmed the presence of gallstones and chronic cholecystitis. Because of the effective preoperative assessment, the patient recovered smoothly and was discharged 3 days after surgery, reporting no discomfort during follow-up.

Conclusion: This case highlights the need for thorough evaluation of rare gallbladder anomalies; literature recommends removing both to prevent disease recurrence. We present this case to raise clinical awareness, support appropriate diagnosis, and reinforce the recommendation to remove both gallbladders to prevent recurrence of gallbladder disease.

腹腔镜下治疗双胆囊双胆囊结石1例。
背景:双胆囊伴两条完全独立的胆囊管是一种非常罕见的先天性异常。本病例报告记录了一个成功的腹腔镜治疗的例子,通过强调准确的术前成像和手术计划的重要性,增加了有限的文献。病例总结:我们报告了一名46岁的维吾尔族妇女,她因间歇性右上腹部疼痛并伴有恶心和呕吐而入院,持续了1周。她的基本血液检查结果,包括肝功能检查,都是正常的。术前超声显示胆囊区回声异常,提示双胆囊畸形,其中一腔内有多发结石。计算机断层扫描和磁共振胆管造影证实双胆囊异常。患者随后接受了成功的腹腔镜胆囊切除术。在手术过程中,确定了两个胆囊腔,每个胆囊管分别插入总胆管。手术完成无并发症,术后病理证实存在胆结石和慢性胆囊炎。由于术前评估有效,患者恢复顺利,术后3天出院,随访期间无不适。结论:本病例强调了对罕见的胆囊异常进行全面评估的必要性;文献建议切除两者以预防疾病复发。我们提出这个病例是为了提高临床意识,支持适当的诊断,并加强切除双胆囊以防止胆囊疾病复发的建议。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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