Zakaria Hazem Mohamed, Gad Emad Hamdy, Gaballa Nahal Kamel, Sallam Ahmed Nabil, Ayoub Islam Ismail, Eltabbakh Mohamed, Elkholy Shimaa Saad, Abokoura Sameh, Yassein Taha, Hegazy Osama, Abdelmeguid Shoreem Hany, Mohamed Soliman Hossam Eldeen, Aziz Amr Ahmed, Taha Mohammad
-Department of Hepatopancreatobiliary and Liver Transplant Surgery, National Liver Institute, Menoufia University, Menoufia, Egypt.
-Department of Anesthesia and Intensive Care, National Liver Institute, Menoufia University, Menoufia, Egypt.
Ann Med Surg (Lond). 2022 Sep 15;82:104714. doi: 10.1016/j.amsu.2022.104714. eCollection 2022 Oct.
There are still debates regarding using portal vein (PV) from liver with hepatocellular carcinoma (HCC) for vascular reconstruction. This study aimed to assess the feasibility and patency of PV venous graft from an explanted liver with HCC for the reconstruction of the hepatic veins tributaries or PV in living donor liver transplantation (LDLT) and to see if it has any risk on recurrence of HCC.
We conducted a retrospective study on 81 patients with HCC who underwent LDLT from April 2004 to July 2022.
Venous graft from native liver PV was used for vascular reconstruction in 31 patients as follows; reconstruction of V5 in 7 patients, V8 in 4 patients, V6 in 3 patients, combined V5 and V8 in 4 patients, V6 with V5/V8 in 5 patients, and as Y shape venous graft for 2 PV reconstruction in 8 patients. The implantation of the new conduit PV graft after reconstruction of the anterior sector tributaries was direct to the IVC in 8 patients, and to the common orifice of the left and middle hepatic veins in 12 patients. The 1 month, 3 months, and 1-year overall patency of the venous graft was 93.5%, 90.3%, and 84%, respectively. Nine patients had recurrent HCC. In multivariate analysis, the independent risk factors for HCC recurrence were AFP >400 ng/mL (HR = 1.47, 95% CI: 1.69-2.31, P = 0.01), moderate/poor differentiated tumor (HR = 3.06, 95% CI: 2.58-6.29, P = 0.02), and microvascular invasion (HR = 2.51, 95% CI: 1.05-1.93, P = 0.01). Using a PV venous graft had no risk factor for HCC recurrence (P = 0.9).
The use of PV venous graft of native liver with HCC for venous reconstruction is a feasible and valuable option in LDLT with good patency rates and no risk of HCC recurrence.
关于在肝细胞癌(HCC)患者的肝脏中获取门静脉(PV)用于血管重建仍存在争议。本研究旨在评估在活体肝移植(LDLT)中,使用来自患有HCC的离体肝脏的PV静脉移植物重建肝静脉分支或PV的可行性和通畅率,并观察其是否存在HCC复发风险。
我们对2004年4月至2022年7月期间接受LDLT的81例HCC患者进行了回顾性研究。
31例患者使用来自自体肝脏PV的静脉移植物进行血管重建,具体如下:7例患者重建V5,4例患者重建V8,3例患者重建V6,4例患者联合重建V5和V8,5例患者重建V6与V5/V8,8例患者将其作为Y形静脉移植物用于2次PV重建。在前段分支重建后,新的导管PV移植物植入,8例患者直接植入下腔静脉,12例患者植入左、中肝静脉的共同开口处。静脉移植物1个月、3个月和1年的总体通畅率分别为93.5%、90.3%和84%。9例患者出现HCC复发。多因素分析显示,HCC复发的独立危险因素为甲胎蛋白>400 ng/mL(HR = 1.47,95%CI:1.69 - 2.31,P = 0.01)、肿瘤中/低分化(HR = 3.06,95%CI:2.58 - 6.29,P = 0.02)和微血管侵犯(HR = 2.51,95%CI:1.05 - 1.93,P = 0.01)。使用PV静脉移植物并非HCC复发的危险因素(P = 0.9)。
在LDLT中,使用患有HCC的自体肝脏PV静脉移植物进行静脉重建是一种可行且有价值的选择,通畅率良好且无HCC复发风险。