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Perihilar cholangiocarcinoma (pCCA) is the most common subtype of extrahepatic bile duct cancer, accounting for approximately 50%-60% of all cholangiocarcinomas. It primarily arises at the confluence of the common hepatic duct and the left and right hepatic ducts1. Due to its unique anatomical location adjacent to the proper hepatic artery, portal vein, and bilateral hepatic ducts, the tumor frequently invades vascular and biliary structures, resulting in significant surgical challenges2 .
Currently, curative resection remains the only treatment modality associated with long-term survival for pCCA. Specifically, left hemihepatectomy combined with caudate lobectomy and regional lymphadenectomy is considered the standard surgical approach for Bismuth-Corlette type IIIb pCCA patients3,4. The necessity of caudate lobectomy based on anatomical resection principles has been confirmed by multiple studies, demonstrating its role in significantly increasing R0 resection rates and reducing local recurrence5. However, dense adhesion or encasement of the tumor around the right hepatic artery and the proper hepatic artery markedly increase intraoperative risk. The limited operating space under laparoscopy further challenges meticulous dissection and vascular preservation, demanding high technical expertise from the surgeon6,7.
With the advancement of laparoscopic techniques, minimally invasive radical resection for hilar cholangiocarcinoma has gradually been performed by experienced surgeons. Nevertheless, due to high surgical risks and a steep learning curve, such procedures are mainly confined to specialized high-volume centers8. Previous literature has primarily focused on right hemihepatectomy, with relatively few reports on laparoscopic left hemihepatectomy combined with caudate lobectomy, especially in cases complicated by close adherence or adhesion to the proper and right hepatic arteries9.
This study presents a case of laparoscopic left hemihepatectomy combined with caudate lobectomy and regional lymphadenectomy for type IIIb hilar cholangiocarcinoma. The major intraoperative challenges included safe and effective separation of the hepatic arteries adherent to the tumor, biliary resection, and hilar dissection. The procedure aimed to achieve oncological radicality while minimizing intraoperative bleeding and complications. This case serves as a valuable technical reference for the laparoscopic management of complex hilar cholangiocarcinoma.
CASE PRESENTATION:
The patient was a 53-year-old male laborer who had been living in a rural area with moderate access to healthcare. He presented to the hospital on May 14, 2024, with a 14-day history of progressive jaundice involving the skin and sclera. The patient reported persistent upper abdominal discomfort and fatigue, accompanied by significant yellow discoloration of the skin and sclera. He also noted an unintentional weight loss of approximately 5 kg over the past 3 months. There were no symptoms of fever, chills, or melena.
The patient had no prior history of liver disease, viral hepatitis (HBV or HCV), cirrhosis, or fatty liver disease. There was no known family history of liver or other cancers. He denied a history of smoking, alcohol consumption, or any other chronic underlying diseases such as diabetes or hypertension. There was no prior surgical history.
An abdominal CT scan performed at an outside facility prior to admission revealed a mass-like lesion in the left hepatic lobe near the hepatic hilum. Cholangiocarcinoma was suspected based on imaging and clinical presentation. The initial diagnosis was perihilar cholangiocarcinoma.
On physical examination, the patient appeared moderately nourished, with marked jaundice of the skin and sclera. There was no lower extremity edema. The abdomen was soft with mild tenderness in the upper abdomen, without palpable masses. The liver and spleen were not enlarged, and there were no signs of ascites. The patient had not received any treatment prior to admission, and this was his first visit to our hospital.
Diagnosis, Assessment, and Plan: The patient was admitted due to progressive skin and scleral jaundice. On admission, physical examination revealed marked jaundice. Laboratory investigations showed elevated cholestatic liver enzymes and tumor markers: CA19-9 was 116 U/mL, gamma-glutamyl transferase (GGT) 183.00 U/L, alkaline phosphatase (ALP) 391.00 U/L, total bilirubin (TBIL) 296.50 µmol/L, and direct bilirubin (DBIL) 183.12 µmol/L. Other tumor markers, coagulation profile, renal function, and transaminase levels were within normal limits. Following admission, enhanced liver MRI with hepatocyte-specific contrast (EOB-MRI) and magnetic resonance cholangiopancreatography (MRCP) were performed, which revealed significant stenosis of the hilar bile duct, consistent with perihilar cholangiocarcinoma (also known as Klatskin tumor).
Preliminary diagnosis: Perihilar cholangiocarcinoma (Klatskin tumor)
Tumor staging: According to the 8th edition of the American Joint Committee on Cancer (AJCC) staging system10, the tumor was staged as cT2NxM0, Bismuth-Corlette Classification11 Type IIIb (involving the left hepatic duct, with no right hepatic duct involvement)
Initial management: Upon admission, the patient received intravenous cefoperazone to prevent infection, hepatoprotective agents, and supportive care, including fluid and electrolyte management. To alleviate biliary obstruction, the patient underwent percutaneous transhepatic cholangial drainage (PTCD).
Reassessment after PTCD: Post-drainage laboratory evaluation showed ALT 43.50 U/L, TBIL 151.76 µmol/L, and DBIL 102.17 µmol/L, indicating sufficient hepatic function for surgical intervention.
Planned surgical procedure: After comprehensive evaluation of the patient's general condition and imaging findings, the following laparoscopic surgical procedure was scheduled: Laparoscopic left hemihepatectomy, Caudate lobe resection, Hilar lymphadenectomy, Cholecystectomy, Hepaticojejunostomy.