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156 C. Lim et al.
Fig. 11.9 Venovenous bypass. a, b Dissection and cannulation of the inferior mesenteric vein. c Percutaneous cannulation of the right femoral vein. d Percutaneous cannulation of the left
axillary vein. e, f Extracorporeal circulation
thermistor probe thermometer into the future liver remnant. Topical cooling of the liver remnant was also applied.
In our patient, an anterior approach technique was performed because of the potential adherence between the posterior mass and the replaced IVC. Then, the right liver was fully mobilized to expose the root of the right hepatic vein, which was ligated and divided. When the liver transection was completed, the liver was flushed with serum albumin (500 mL) via the portal vein. The cannula of portal perfusion and the caval drainage were then removed. The portal vein hole was rinsed with heparin and sutured transversally with interrupted vascular sutures to prevent stenosis. Circulation was then restored as for standard TVE. The portal cannula of the bypass was clamped quickly upon revascularization of the remaining left liver to optimize portal reperfusion. The bypass was stopped and removed when hemodynamic stability was confirmed by the anesthesiologists. Doppler ultra­sonography was used to assess the patency of vessels. The Doppler imaging also helped optimize the position of the remaining liver by preventing any vascular kinking of the hepatic veins or the suprahepatic vena cava. The venovenous bypass lasted 120 min and TVE 55 min. Blood loss was 1000 ml. The patient received two units of packed red blood cells.
11 Resection of Renal Cell Carcinoma Involving the Liver … 157
Fig. 11.10 a Right subcostal incision combined to midline incision. b, c The portal vein was catheterized above the portal triad clamp. d Clamping of the portal triad. e Infrahepatic inferior vena cava clamping (below the prosthetic graft). f Intrapericardial vena cava clamping
Fig. 11.11 The clamp was located below the prosthetic graft
158 C. Lim et al.

Discussion

The main technical aspect which is the in situ hypothermic technique with the use of venovenous bypass of this procedure could be discussed. With the advance in surgical technique, liver resection under hypothermic perfusion remains rare (3% in our experience). It is mainly indicated for tumors invading the cavo-hepatic junc­tion and if complex vascular reconstruction is required for the remnant liver. The majority of patients with “limited vascular invasion or contact” can nowadays be operated on safely with intermittent occlusion of the hepatic pedicle. Another possibility could be to start the hepatic transection under intermittent clamping of the hepatic pedicle and apply short TVE when approaching the vascular contact with the replaced IVC. In this case, isolated occlusion of the replaced IVC should be avoided to limit postoperative IVC thrombosis.
Alternatives Approaches
• The decision to proceed for IVC reconstruction should depend upon preoperative criteria (lower extremity edema, collateral venous pathways on the radiological imaging).
• The IVC reconstruction is not without postoperative risks, including thrombosis and sepsis.
• In case of IVC resection combined with right nephrectomy, left renal vein reconstruction is not mandatory. But in case of IVC resection with left nephrectomy, right renal vein reconstruction is mandatory.

Short-Term Outcome

The postoperative course was uneventful. The patient did not experience postop­erative liver failure or acute kidney injury. The liver tests were normal at discharge. Postoperative MDCT was normal and show patency of the replaced IVC (Fig. 11.12).
In our reported experience, this complex procedure performed for primary and secondary liver tumors achieved a five-year survival rate of 30.4% and a high 90-day mortality of 19.5% [13]. Risk factors for postoperative mortality include Charlson comorbidity index 3 (indicating at least 2 comorbid conditions), maximum tumor diameter 10 cm, and the presence of 50/50 criteria on post­operative day 5 were independent predictors of surgical mortality measured at 90 days.
11 Resection of Renal Cell Carcinoma Involving the Liver … 159
Fig. 11.12 Postoperative computed tomography after right hepatectomy
160 C. Lim et al.

Long-Term Outcome

RCC can metastasize to almost every organ. Metastatic RCC represent 30% of RCC at diagnosis and occur in 15–30% following nephrectomy [25–27]. The most common metastatic sites include lung (50–60%), bone (30–40%), liver (30–40%), and brain (5%). Unusual sites of metastases include thyroid, pancreas, muscle, and skin [28]. To date, the European Association of Urology recommended in their guidelines that surgical resection of metastases from RCC should be considered for most metastatic sites, with the exception of brain and bones. To date, surgical resection remains the only curative treatment of metastases from RCC with a five-year survival rate of 30–45% for patients who underwent surgical resection of metastases whatever the sites [29–32]. Surgery for the metastases from RCC can be proposed if it concerns an isolated metastatic site and if complete resection can be achieved regardless of the length of the disease-free interval (synchronous vs. metachronous) [33]. Of course, a longer disease-free interval foll owing nephrec­tomy has been shown to be a positive prognostic factor [34].
Survival data reported from targeted therapy clinical trials showed a median overall survival between 26.4 and 32 months for patients who received sunitinib or combined sunitinib and everolimus [35, 36].
Liver metastases from RCC, like any other metastatic lesions, can be treated by surgery, systemic chemotherapy, radiotherapy, percutaneous ablation, and transar­terial chemoembolization. Su rgical resection of liver metastases from RCC achieved survival rates of 26–54% at 3 years with a median survival time reaching 48 months. The three-year survival rates for patients treated by chemotherapy and interferon were 15 and 48%, respec tively [28]. Although TACE can result in a favorable local tumor response, survival rates are less favorable than those achieved by surgery with one- and two-year survival rates (from the start of treatment) for patients treated with TACE of 31 and 6%, respectively, with a median survival time of 8.8 months [37].
In our case, the patient recurred in the liver 15 months later following right nephrectomy and IVC thrombectomy for a RCC with tumor thrombus extending into the retrohepatic IVC.
Global Pearls
• The anatomic level of the tumor thrombus within the inferior vena cava according to the classification by Neves and Zincke dictates the surgical strategy.
• Surgery of the IVC requiring infrahepatic and retrohepatic inferior vena cava (below the level of the hepatic veins) control are usually well tol­erated in terms of hemodynamics, especially when the inferior vena cava is completely obstructed by the thrombus. While surgery of the IVC combined with standard total vascular exclusion of the liver can induce hemodynamic consequences with a risk of postoperative liver failure.
11 Resection of Renal Cell Carcinoma Involving the Liver … 161
• Use of venovenous bypass and hypothermic perfusion of the liver can decrease the risk of postoperative liver failure, particularly when a vas­cular reconstruction is needed or standard vascular exclusion of the liver is planned to last >60 min.

References

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31. Kierney PC, van Heerden JA, Segura JW, Weaver AL. Surgeon’s role in the management of solitary renal cell carcinoma metastases occurring subsequent to initial curative nephrectomy: an institutional review. Ann Surg Oncol. 1994;1(4):345–52.
32. Motzer RJ, Bacik J, Schwartz LH, Reuter V, Russo P, Marion S, et al. Prognostic factors for survival in previously treated patients with metastatic renal cell carcinoma. J Clin Oncol. 2004;22(3):454–63.
33. Jakubowski CD, Vertosick EA, Untch BR, et al. Complete metastasectomy for renal cell carcinoma: comparison of five solid organ sites. J Surg Oncol. 2016;114(3):375–9.
34. Hofmann HS, Neef H, Krohe K, Andreev P, Silber RE. Prognostic factors and survival after pulmonary resection of metastatic renal cell carcinoma. Eur Urol. 2005;48(1):77–81; discussion 81–2.
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36. Motzer RJ, Barrios CH, Kim TM, Falcon S, Cosgriff T, Harker WG, et al. Phase II randomized trial comparing sequential first-line everolimus and second-line sunitinib versus first-line sunitinib and second-line everolimus in patients with metastatic renal cell carcinoma. J Clin Oncol. 2014;32(25):2765–72.
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Part II

Gallbladder/Bile Duct

Hilar Cholangiocarcinoma with Portal Vein Involvement

Ryan T. Groeschl and David M. Nagorney

Case Presentation

A 64-year-old man with several years of diarrhea and crampy abdominal pain underwent CT enterography. Assessment of the liver demonstrated severe atrophy of the left lobe, with the absence of a visible left portal vein (Fig. 12.1). He was not jaundiced. Serum bilirubin was normal and CA 19-9 was 76 U/mL. His past medical and surgical history was non-contributory.
A contrast-enhanced MRI with MRCP was obtained to further characterize the liver and bile ducts, particularly at the hepatic hilus. MRI reveal ed a distinct 2.7 cm mass in the left lobe that caused a tight stenosis of the main left hepatic duct without visualization of the left portal vein (Fig. 12.2). There was also irregular contour of the common hepatic duct on MRCP. The clinical diagnosis was type IIIb HC. There was no evidence of distant disease on either CT or MRI. No effort was made to obtain a tissue diagnosis preoperatively.
The complete absence of a visible left portal vein supported the preoperative assumption of malignant obstruction of the left portal vein. The presence of lobar hepatic atrophy and the absence of jaundice and cholangitis obviated the need for any preoperative intervention. An en-bloc left hepatectomy, extrahepatic bile duct resection, regional lymphadenectomy, and Roux-en-Y hepaticojejunostomy were performed. Intraoperatively, the malignant involvement of the left portal vein
12
R.T. Groeschl (&) D.M. Nagorney Department of Surgery, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA e-mail: groeschl.ryan@mayo.edu
D.M. Nagorney e-mail: nagorney.david@mayo.edu
© Springer International Publishing AG 2017 T.M. Pawlik et al. (eds.), Case-Based Lessons in the Management of Complex Hepato-Pancreato-Biliary Surgery, DOI 10.1007/978-3-319-50868-9_12
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