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Background: While robotic liver surgery has been widely established, major liver resection with biliary reconstruction remains challenging.
Methods: A 54-year-old female presenting with painless jaundice was diagnosed with a perihilar cholangiocarcinoma Bismuth IIIb. The indication for resection was confirmed by the multidisciplinary tumor board. We performed a left hepatectomy (H1234-B) with en-bloc resection of the extrahepatic bile duct using the Intuitive Surgical DaVinci Xi system. A tip-up fenestrated grasper, a fenestrated bipolar forceps, and a synchro-seal were used for resection. A 12 mm and a 5 mm laparoscopic trocar were placed for assistance. Hilar lymphadenectomy was performed for the stations 12a, 8a, 9, 7, 12b, and 12p. The clamp-crush-technique was applied for parenchymal dissection and the right hilar plate was dissected with robotic scissors. The caudate lobe was detached from the retrohepatic vena cava and short veins were clipped. The posterolateral and anteromedial bile ducts were reconstructed with two jejunostomies using PDS 5-0 running sutures. Biliary stents (9 French) were placed in each anastomosis. Retrieval of the specimen and a Roux-en-Y- jejunojejunostomy were performed via an umbilical mini-laparotomy.
Results: The operation time was 498 min, the cumulative Pringle time during parenchymal transection was 43min. R0 resection was achieved and 26 lymph nodes were retrieved. The postoperative course was uneventful and the patient was discharged on postoperative day 10.
Discussion: This video supports previous reports demonstrating that the DaVinci Xi surgical system can safely perform even highly complex liver resections with biliary reconstruction. While techniques and strategies in laparoscopic liver surgery have become increasingly harmonized in recent years, there are still major inter-center differences in robotic liver surgery. The video demonstrates in detail each relevant step of a robotic left hepatectomy with biliary reconstruction and highlights our center-specific strategies, techniques, and approaches.
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http://dx.doi.org/10.1245/s10434-025-17018-0 | DOI Listing |
Ann Surg Oncol
September 2025
Department of Hepatobiliary-Pancreatic Surgery, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Background: Right-sided hepatectomy (RH) is the standard surgical approach for perihilar cholangiocarcinoma (PHC) due to anatomical considerations but is associated with a high risk of post-hepatectomy liver failure (PHLF). Left-sided hepatectomy (LH) and central hepatectomy (CH) have been proposed as alternative strategies to preserve liver function, but the feasibility and outcomes of CH have not been sufficiently investigated. CH allows for greater preservation of liver parenchyma, potentially reducing the risk of PHLF.
View Article and Find Full Text PDFWorld J Hepatol
August 2025
Department of General Surgery, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen 518107, Guangdong Province, China.
Background: Adrenal ectopia is a rare condition in which adrenal tissue is found in an abnormal location, often posing diagnostic challenges. Although generally considered benign, it can present as hepatic or other organ lesions, mimicking malignant tumors. In the liver, ectopic adrenal tissue can closely resemble hepatocellular carcinoma or metastatic disease, potentially leading to unnecessary aggressive treatments such as surgery or chemotherapy.
View Article and Find Full Text PDFInt J Surg Case Rep
August 2025
Department of General Surgery of the Faculty of Medicine, Damascus University, Damascus, Syrian Arab Republic. Electronic address:
Background: Todani Type IVa choledochal cysts are rare congenital malformations involving both intrahepatic and extrahepatic bile ducts. Adult-onset, asymptomatic, and localized presentations are exceptionally uncommon and pose a surgical challenge, particularly when considering the extent of resection and reconstruction required.
Case Presentation: We report the case of a 24-year-old asymptomatic female who was incidentally diagnosed with a localized Todani Type IVa cyst involving the left hepatic lobe and the common bile duct.
J Gastrointest Cancer
August 2025
The Third Bethune Hospital of Jilin University, Changchun, Jilin, China.
Introduction: Intrahepatic biliary neuroendocrine neoplasms (NENs) are rare neoplasms originating from neuroendocrine cells in the intrahepatic bile ducts. Patients often present without hormone-related symptoms but are admitted due to jaundice or abdominal pain.
Presentation Of Case: This case report describes a 57-year-old female patient who experienced intermittent upper abdominal pain for one month prior to admission.
J Surg Case Rep
August 2025
Department of Surgery (A), Heinrich-Heine-University, Medical Faculty and University Hospital Duesseldorf, Moorenstr. 5, 40225 Duesseldorf, North Rhine-Westphalia, Germany.
Caroli's disease is a rare congenital disorder characterized by cystic dilatations of the intrahepatic bile ducts, often leading to recurrent bacterial cholangitis, biliary lithiasis, and cirrhosis. In 7%-16% of cases, it progresses to intrahepatic cholangiocarcinoma, emphasizing the need for early diagnosis and intervention. This report presents a 56-year-old patient with recurrent upper abdominal pain, chronic fatigue, and night sweats.
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