Bourabaa Soukayna, Laalou Talha, Mansouri Abderrahman, Hamid Mohamed, Settaf Abdellatif
General Surgery Department, Ibn Sina University Hospital, Rabat, Morocco.
Mohammed V University, Rabat, Morocco.
BMC Surg. 2025 May 15;25(1):214. doi: 10.1186/s12893-025-02948-z.
Caroli disease is an uncommon congenital condition characterized by non-obstructive intrahepatic bile duct dilation. When coupled with liver fibrosis or cirrhosis, it is termed Caroli syndrome. This disorder can lead to the development of gallstones, inflammation of the bile ducts, and an elevated susceptibility to cholangiocarcinoma. Typically, Caroli disease presents with involvement in less than 20% of the liver, predominantly affecting a single lobe (either left or right). Monolobar disease can often be effectively addressed through liver resection, while bilobar disease may necessitate the consideration of liver transplantation.
A retrospective study was undertaken involving patients diagnosed with Caroli disease who underwent liver resection. The research included cases from Surgery B Department at Ibn Sina University Hospital in Rabat, covering the period from January 2010 to January 2023.
Nine patients who underwent liver resection for Caroli disease were identified, with an average age of 54 years (range: 17-76), and 44.4% (n = 4) being females. The study comprised 6 cases with disease limited to the left lobe and 3 to the right. The average time interval between initial symptoms and the definitive diagnosis was 4 years (range: 0-24 years). Surgical procedures included left lobectomy in 4 cases, left hepatectomy in 3 cases, right hepatectomy in 1 case, and sub-segmentectomy in 2 cases. Biliodigestive anastomosis was performed in 4 cases. Complications occurred in 2 patients (22.2%), and synchronous cholangiocarcinoma was observed in a single case (11.1%).
Consideration of Caroli disease as part of the differential diagnosis is crucial in cases of recurrent cholangitis. Liver resection stands out as the treatment of choice for patients with localized Caroli disease. The critical importance of early intervention is highlighted by the potentially fatal consequences of delayed diagnosis or treatment.
卡罗里病是一种罕见的先天性疾病,其特征为非梗阻性肝内胆管扩张。当合并肝纤维化或肝硬化时,则称为卡罗里综合征。这种疾病可导致胆结石形成、胆管炎症,并增加患胆管癌的易感性。通常情况下,卡罗里病累及肝脏的比例不到20%,主要影响单个肝叶(左叶或右叶)。单叶病变通常可通过肝切除术有效治疗,而双叶病变可能需要考虑肝移植。
对诊断为卡罗里病并接受肝切除术的患者进行了一项回顾性研究。该研究纳入了拉巴特伊本·西那大学医院外科B科2010年1月至2023年1月期间的病例。
确定了9例因卡罗里病接受肝切除术的患者,平均年龄54岁(范围:17 - 76岁),女性占44.4%(n = 4)。该研究包括6例病变局限于左叶的病例和3例局限于右叶的病例。初始症状与明确诊断之间的平均时间间隔为4年(范围:0 - 24年)。手术方式包括4例左叶切除术、3例左半肝切除术、l例右半肝切除术和2例亚段切除术。4例患者进行了胆肠吻合术。2例患者(22.2%)出现并发症,1例患者(11.1%)观察到同步性胆管癌。
在复发性胆管炎病例中,将卡罗里病纳入鉴别诊断至关重要。肝切除术是局限性卡罗里病患者的首选治疗方法。延迟诊断或治疗可能导致致命后果,这凸显了早期干预的至关重要性。