Bile duct injury

胆管损伤
  • 文章类型: Case Reports
    重复的胆囊管是一种罕见的先天性畸形,在2019年之前报告的病例少于20例。这种畸形对于确定降低术中并发症的风险很重要,例如胆管损伤会增加术后发病率和死亡率。我们介绍了一名62岁的男性,其重复的胆囊管在腹腔镜胆囊切除术中结扎,随后并发术后胆汁瘤形成。胆漏的治疗选择包括内镜逆行胰胆管造影术(ERCP)和支架置入术,经皮引流,和导管栓塞。每个都有感染等并发症的风险,管道穿孔,和支架/引流位移。当其他微创手术失败时,Roux-en-Y肝空肠吻合术(RHYJ)往往是最后的手段。必须确定与胆囊管异常相关的术后并发症以及发生这些并发症时可用的各种治疗方案。
    Duplicated cystic ducts are a rare congenital malformation with less than 20 reported cases before 2019. This malformation is important to identify to reduce the risk of intraoperative complications such as bile duct injuries that can increase postoperative morbidity and mortality. We present the case of a 62-year-old male with duplicated cystic ducts that were ligated during laparoscopic cholecystectomy and subsequently complicated by postoperative biloma formation. Treatment options for biliary leak include endoscopic retrograde cholangiopancreatography (ERCP) with stenting, percutaneous drainage, and duct embolization. Each carries the risk of complications such as infection, duct perforation, and stent/drain displacement. Roux-en-Y hepaticojejunostomy (RHYJ) tends to be the last resort when other minimally invasive procedures fail. It is imperative to identify postoperative complications related to cystic duct anomalies and the various treatment options available should these complications occur.
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  • 文章类型: Case Reports
    背景:任何原因造成的胆管损伤对患者来说都是灾难,对外科医生构成了重大的心理和技术挑战。使用肝圆韧带和胆囊皮瓣作为自体移植物在修复胆管损伤方面显示出有希望的结果。
    方法:本文介绍了一个具有挑战性的Mirizzi综合征患者,该患者在胆囊切除术中经历了复杂的胆管缺损和损伤。我们描述了同时使用肝圆韧带和残余胆囊皮瓣成功重建胆管的方法。
    结论:肝韧带和残余胆囊皮瓣容易获得,是修复和重建胆管损伤的理想修复材料。良好的组织相容性,术后并发症发生率低。在手术中发生胆管损伤时,必须寻求经验丰富的胆道外科医生的帮助。
    结论:肝圆韧带和胆囊瓣,作为合适的自体组织,是修复胆管损伤和缺损的可行选择。
    BACKGROUND: Bile duct injuries caused by any reason are a disaster for patients and pose a significant psychological and technical challenge for surgeons. The use of Ligamentum teres hepatis and gallbladder flap as autografts is showing promising results in the repair of bile duct injury.
    METHODS: This article presents a challenging case of a patient with Mirizzi syndrome who experienced a complex bile duct defect and injury during cholecystectomy. We describe the successful reconstruction of the bile duct using ligamentum teres hepatis and remnant gallbladder flap simultaneously.
    CONCLUSIONS: Ligamentum teres hepatis and remnant gallbladder flap are ideal repair materials for repairing and reconstructing bile duct injuries due to their easy availability, good tissue compatibility, and low incidence of postoperative complications. It is essential to seek the assistance of an experienced biliary surgeon when bile duct injury occurs during operation.
    CONCLUSIONS: Ligamentum teres hepatis and gallbladder flap, as suitable autologous tissues, are viable options for repairing bile duct injuries and defects.
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  • 文章类型: Case Reports
    腹腔镜胆囊切除术后胆管损伤,尤其是Luschka的管道,是有关的。根据一个病例报告了胆道异常和静脉内施用Gd-EOB-DTPA增强的磁共振成像(MRI)在检测胆漏中的功效。教学要点:肝胆特异性MRI造影剂被证明对胆囊切除术后胆漏的无创评估有价值。
    Post-laparoscopic cholecystectomy bile duct injuries, especially involving Luschka\'s duct, are concerning. Biliary tree anomalies and the efficacy of intravenous administration of Gd-EOB-DTPA-enhanced magnetic resonance imaging (MRI) in detecting bile leakage are reported based on a case. Teaching Point: Hepatobiliary-specific MRI-contrast agents prove valuable for noninvasive assessment of bile leakage after cholecystectomy.
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  • 文章类型: Case Reports
    胆道系统和胃肠道之间内瘘的形成是一种罕见的疾病,具有各种病因,主要与胆道系统和肿瘤的复发性慢性炎症有关。有这种情况的患者可能缺乏特定的临床表现,出现腹痛等症状,发烧,黄疸,或者可能根本没有临床症状。常见的内瘘类型包括胆囊十二指肠瘘,胆囊结肠瘘,和胆总管十二指肠瘘.其中,右肝十二指肠瘘极为罕见,在临床文献中很少报道。我们在此报告一例右肝十二指肠瘘,并分析其机制,治疗原则,并通过文献综述采取预防措施。
    The formation of an internal fistula between the biliary system and the gastrointestinal tract is a rare condition with various etiologies, predominantly associated with recurrent chronic inflammation of the biliary system and tumors. Patients with this condition may lack specific clinical manifestations, presenting with symptoms such as abdominal pain, fever, jaundice, or may show no clinical signs at all. Common types of internal fistulas include cholecystoduodenal fistula, cholecystocolonic fistula, and choledochoduodenal fistula. Among these, the right hepaticoduodenal fistula is extremely rare and seldom reported in clinical literature. We herein report a case of right hepaticoduodenal fistula and analyze its mechanism, treatment principles, and preventive measures through a literature review.
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  • 文章类型: Case Reports
    Mirizzi综合征,胆石症的罕见并发症,涉及胆结石导致肝总管受压。它带来了非特异性症状的诊断挑战。早期识别和手术干预至关重要,强调多学科的方法,这种复杂的条件与潜在的并发症。
    方法:一名69岁女性出现瘙痒,黄疸,还有肝绞痛病史.实验室结果显示无炎症迹象,但提示胆汁淤积。影像学提示Mirizzi综合征1型,经MRI证实。病人接受了手术,显示II型Mirizzi综合征,存在胆囊胆总管瘘,占不到主胆管周长的三分之一。进行了胆囊大部切除术和将主胆管缝合到T形管上,导致10天后血液检查的良好恢复和正常化。
    Mirizzi综合征,以外科医生PabloLuisMirizzi的名字命名,在1948年首次详细介绍。临床症状包括黄疸,绞痛,以及胆囊胆总管瘘和胆石性肠梗阻等并发症。血液检查和成像辅助诊断。手术治疗的目标是缓解梗阻和修复缺损。解剖卡洛的三角形有风险。在复杂的情况下,可以考虑胆囊-胆总管-十二指肠造口术。
    结论:Mirizzi综合征,一种罕见但意义重大的疾病,需要仔细的临床注意,以防止诊断不足。及时和适当的管理,与ERCP一起使用成像测试,对于最佳结果和并发症预防至关重要。
    UNASSIGNED: Mirizzi syndrome, a rare complication of cholelithiasis, involves gallstones causing common hepatic duct compression. It poses diagnostic challenges with nonspecific symptoms. Early recognition and surgical intervention are crucial, emphasizing a multidisciplinary approach for this complex condition with potential complications.
    METHODS: A 69-year-old woman presented with pruritus, jaundice, and a history of hepatic colics. Laboratory results showed no signs of inflammation but indicated cholestasis. Imaging suggested Mirizzi syndrome type 1, confirmed by MRI. The patient underwent surgery, revealing Mirizzi syndrome type II with the presence of a cholecystocholedochal fistula involving less than one-third of the circumference of the main bile duct. Subtotal cholecystectomy and suturing of the main bile duct onto a T-tube were performed, resulting in a favorable recovery and normalization of blood tests after 10 days.
    UNASSIGNED: Mirizzi syndrome, named after surgeon Pablo Luis Mirizzi, was first detailed in 1948. Clinical symptoms include jaundice, colic pain, and complications such as cholecystocholedochal fistula and gallstone ileus. Blood tests and imaging aid diagnosis. Surgical management targets obstruction relief and defect repair. Dissecting Calot\'s triangle carries risks. In complex cases, cholecysto-choledocus-duodenostomy may be considered.
    CONCLUSIONS: Mirizzi syndrome, a rare but significant condition, demands careful clinical attention to prevent underdiagnosis. Timely and appropriate management, utilizing imaging tests alongside ERCP, is essential for optimal outcomes and complication prevention.
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  • 文章类型: Case Reports
    Mirizzi syndrome is a rare chronic cholecystitis complication. However, the current consensus on managing this condition remains controversial, especially through laparoscopic surgery. This report describes the feasibility of treating type I Mirizzi syndrome with laparoscopic subtotal cholecystectomy and electrohydraulic lithotripsic gallstone removal. A 53-year-old woman presented with dark urine and right upper quadrant pain for 1 month. On examination, she was jaundiced. Blood tests showed highly elevated liver and biliary enzyme levels. Abdominal ultrasound showed a slightly dilated common bile duct with suspicion of choledocholithiasis. However, endoscopic retrograde cholangiopancreatography showed a narrowed common bile duct extrinsically compressed by a gallstone in the cystic duct, establishing a Mirizzi syndrome diagnosis. Elective laparoscopic cholecystectomy was planned. At operation, the trans-infundibulum approach was used since dissection around the cystic duct was difficult due to severe local inflammation of Calot\'s triangle. The gallbladder\'s neck was opened, and the stone was removed by lithotripsy via a flexible choledochoscope. Common bile duct exploration through the cystic duct was normal. The fundus and body of the gallbladder were resected, followed by T-tube drainage and suturing of the gallbladder\'s neck. The patient\'s postoperative clinical course was uneventful. Treating Mirizzi syndrome remains a major challenge for hepatobiliary specialists even with open surgery due to high complication rates, including bile duct injuries. Treatment is primarily to clear out the responsible stone and necrotic tissue. Due to advances in endoscopic surgery and equipment, subtotal cholecystectomy with laparoscopic gallstone extraction provides a safe and effective option for patients with Mirizzi syndrome. Laparoscopic subtotal cholecystectomy with electrohydraulic lithotripsy is a feasible and useful approach for treating Mirizzi syndrome that avoids iatrogenic bile duct injury.
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  • 文章类型: Case Reports
    医源性胆管损伤仍然是胃肠道手术中的一个重大问题,特别是如果在术后后期发现。在这里,我们报告了一例腹腔镜胆囊切除术后的异常胆漏,其中包括第5段的孤立的右段肝管损伤以及连接胆囊窝和胆总管的小导管的额外胆漏。我们称这种情况为不完全孤立的右段肝管损伤。患者在腹腔镜胆囊切除术后2周出现感染的胆汁瘤。在胆汁瘤的经皮引流和抗生素治疗后,首先通过与胆总管的小连接的线圈栓塞来封闭复杂的胆瘘,然后通过顺行和逆行的组织动脉栓塞来封闭,从而在一个疗程中造成完全孤立的右段肝管损伤。患者当天出院,恢复无并发症或复发。
    Iatrogenic bile duct injuries remain a substantial problem in gastrointestinal surgery, especially if discovered later in the postoperative period. Herein, we report a case of an unusual bile leak following laparoscopic cholecystectomy consisting of an isolated right segmental hepatic duct injury of segment 5 together with an additional bile leak of a small duct connecting the gallbladder fossa with the common bile duct. We call this situation an incomplete isolated right segmental hepatic duct injury. Patient presented with infected biloma 2 weeks after laparoscopic cholecystectomy. After percutaneous drainage of the biloma and antibiotic therapy the complex biliary fistula was closed first with coil embolization of the small connection to the common bile duct and then with both antegrade and retrograde histoacryl embolization of the hereby created complete isolated right segmental hepatic duct injury in a single session. Patient was discharged the same day and recovered without complication or recurrence.
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  • 文章类型: Case Reports
    背景:关于肝切除术后胆管损伤(PHBDI)的文献有限,缺乏大样本的回顾性研究和高质量的经验总结。因此,我们报道了一例特殊的医源性胆管损伤的病例,该病例是在右肝切除术中,由血管内胃肠道吻合术(endo-GIA)引起的,分析了这种伤害的原因,并总结了这位患者的经验。
    方法:我们介绍了一例66岁女性,因肝内胆管扩张(Caroli病)而复发性腹痛和胆管炎。术前评估显示病变和扩张的胆管局限于右肝,右肝萎缩,左肝肥大,和肺门易位。这个问题可以通过执行标准的右肝切除术来解决。虽然手术进展顺利,手术后不久出现黄疸。医源性胆管损伤被认为是磁共振胰胆管造影后,第二次手术在10d后进行。在第二次手术中,发现endo-GIA损坏了肝管的侧壁,并且在胆管壁中保留了多个钛钉。这导致管壁严重狭窄,无法修复。因此,受伤的胆管被横断,在左肝管的健康部位进行肝-空肠-外侧Roux-Y吻合术。手术后,病人术后恢复顺利,总胆红素逐渐降至正常。术后41d患者出院。随访6个月未发现吻合口狭窄。
    结论:并非所有病例都适用于Glissonean椎弓根的GIA内切断术,尤其是在肝内胆管病变的病例中。由于广泛的缺血,由endo-GIA引起的PHBDI很难修复,这需要特别注意。
    BACKGROUND: The literature on post-hepatectomy bile duct injury (PHBDI) is limited, lacking large sample retrospective studies and high-quality experience summaries. Therefore, we reported a special case of iatrogenic bile duct injury caused by Glissonean pedicle transection with endovascular gastrointestinal anastomosis (endo-GIA) during a right hepatectomy, analyzed the causes of this injury, and summarized the experience with this patient.
    METHODS: We present the case of a 66-year-old woman with recurrent abdominal pain and cholangitis due to intrahepatic cholangiectasis (Caroli\'s disease). Preoperative evaluation revealed that the lesion and dilated bile ducts were confined to the right liver, with right hepatic atrophy, left hepatic hypertrophy, and hilar translocation. This problem can be resolved by performing a standard right hepatectomy. Although the operation went well, jaundice occurred soon after the operation. Iatrogenic bile duct injury was considered after magnetic resonance cholangiopancreatography review, and the second operation were performed 10 d later. During the second operation, it was found that the endo-GIA had damaged the lateral wall of the hepatic duct and multiple titanium nails remained in the bile duct wall. This led to severe stenosis of the duct wall, and could not be repaired. Therefore, the injured bile duct was transected, and a hepatic-jejunal-lateral Roux-Y anastomosis was performed at the healthy part of the left hepatic duct. After this surgery, the patient had a smooth postoperative recovery, and the total bilirubin gradually decreased to normal. The patient was discharged 41 d after operation. No anastomotic stenosis was found at the 6 mo of follow-up.
    CONCLUSIONS: Not all cases are suitable for endo-GIA transection of Glissonean pedicle, especially in cases of intrahepatic bile duct lesions. PHBDI caused by endo-GIA is very difficult to repair due to extensive ischemia, which requires special attention.
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  • 文章类型: Case Reports
    Biliary anomalies are a high risk for biliary injury during surgery, and although a biliary anomaly is occasionally encountered, variations in cystic ducts are rare. A preoperative diagnosis is highly valuable in facilitating surgical procedures and avoiding surgical complications. Herein, the case of a 67-year-old female patient with acute cholecystitis, in which preoperative fluoroscopic cholangiography clearly demonstrated a single gallbladder with double cystic ducts, is presented. The accessory duct was found to be dominant, draining into the otherwise normal right intrahepatic bile duct, and laparoscopic cholecystectomy was performed smoothly and successfully. Fluoroscopic cholangiography is a powerful tool that may clearly depict the anomaly of a single gallbladder with double cystic ducts. Through appropriate preoperative knowledge and demonstration of this biliary anomaly in the present case, laparoscopic cholecystectomy was safely performed, and the patient was symptom-free at the 3-year follow-up assessment.
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  • 文章类型: Journal Article
    UNASSIGNED: Gallstone disease is common in India, and since primary management involves surgery, it is one of the most commonly performed surgeries by a general surgeon either laparoscopically or open. There are various factors which are responsible for intra- and post-operative complications. These factors result in significant injuries which cause serious post-operative complications. Amongst them, benign biliary stricture is one such significant complication which is primarily managed by open surgery, but since advent of laparoscopy, there has been an increased interest in doing this repair laparoscopically.
    UNASSIGNED: This is a retrospective study of 16 patients having obstructive jaundice due to benign biliary stricture on magnetic resonance cholangiopancreatography who were operated consecutively over the past 10 years laparoscopically and underwent laparoscopic Roux-en-Y hepaticojejunostomy.
    UNASSIGNED: All patients underwent laparoscopic hepaticojejunostomy. The mean surgical time was 280 min, and the mean blood loss was 176 ml. In the post-operative period, most of the patients were started orally after 48 h; four had atelectasis, eight had surgical site infection, none had seroma and two had bile leak. All post-operative complications responded to conservative management.
    UNASSIGNED: The study demonstrates that laparoscopic surgery for benign biliary strictures is safe and feasible with acceptable results.
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