Abdelsalam Ahmed Mohammed, Elansary Ahmed Mohammed Salah Eldeen, Mostafa Ibrahim Mohamed Abdelrahman
Faculty of Medicine, Cairo University, Kasr Alainy St., Cairo, 11562, Egypt.
Int J Surg Case Rep. 2021 Jan;78:116-119. doi: 10.1016/j.ijscr.2020.10.079. Epub 2020 Nov 23.
Abnormal anatomy of the biliary tree predisposes patients to higher risks of ductal injury and postoperative complications. One of the extremely rare abnormalities of the cystic duct is the duplication of the cystic duct with a single gallbladder. The diagnosis is usually established during surgery. we report a case of double cystic duct with literature review.
A forty-two years old female patient who complained of recurrent biliary colic 9 months prior to the presentation. Murphy's sigh was negative and with no other relevant clinical signs.
Abdominal ultrasound showed multiple gall stones; the largest one was about 11 mm in diameter. Laparoscopic cholecystectomy was done under general anesthesia with 4 ports insertion. A double cystic duct accidentally encountered after clipping and cutting what was apparently a single cystic duct. Intraoperative cholangiogram was done to confirm the anomaly and exclude CBD injury.
Double cystic duct is a very rare variant of the cystic duct anomaly. Proper knowledge of this anomaly should be kept in mind to avoid any unnecessary steps.
胆管系统的解剖异常会使患者面临更高的胆管损伤风险和术后并发症风险。胆囊管极其罕见的异常之一是胆囊管重复且胆囊单一。诊断通常在手术过程中确立。我们报告一例双胆囊管病例并进行文献复习。
一名42岁女性患者,在就诊前9个月主诉反复胆绞痛。墨菲氏征阴性,无其他相关临床体征。
腹部超声显示多发胆结石;最大直径约11毫米。在全身麻醉下通过插入4个端口进行腹腔镜胆囊切除术。在夹闭并切断看似单一的胆囊管后意外发现双胆囊管。术中进行胆管造影以确认异常并排除胆总管损伤。
双胆囊管是胆囊管异常中非常罕见的一种变异。应牢记对这种异常的正确认识,以避免任何不必要的步骤。