Ligament D Arantius

World J Gastroenterol. 2017 Nov 7; 23(41): 7433–7439.

The right enables the surgeon to identify the Arantius ligament that is continuous with the lesser omentum. We recently did not transect the lesser omentum because the ventral aspect of the Arantius ligament could be identified easily. Inferior traction was applied to the caudal end of the Arantius ligament, and the liver parenchyma was dissected.

Published online 2017 Nov 7. doi: 10.3748/wjg.v23.i41.7433
PMID: 29151697
This article has been cited by other articles in PMC.

Abstract

AIM

To establish the surgical flow for anatomic isolated caudate lobe resection.

METHODS

The study was approved by the ethics committee of the Second Affiliated Hospital Zhejiang University School of Medicine (SAHZU). From April 2004 to July 2014, 20 patients were enrolled who underwent anatomic isolated caudate lobectomy at SAHZU. Clinical and postoperative pathological data were analyzed.

RESULTS

Of the total 20 cases, 4 received isolated complete caudate lobectomy (20%) and 16 received isolated partial caudate lobectomy (80%). There were 4 cases with the left approach (4/20, 20%), 6 cases with the right approach (6/20, 30%), 7 cases with the bilateral combined approach (7/20, 35%), 3 cases with the anterior approach (3/20, 15%), and the hanging maneuver was also combined in 2 cases. The median tumor size was 5.5 cm (2-12 cm). The median intra-operative blood loss was 600 mL (200-5700 mL). The median intra-operative blood transfusion volume was 250 mL (0-2400 mL). The median operation time was 255 min (110-510 min). The median post-operative hospital stay was 14 d (7-30 d). The 1- and 3-year survival rates for malignant tumor were 88.9% and 49.4%, respectively.

CONCLUSION

Caudate lobectomy was a challenging procedure. It was demonstrated that anatomic isolated caudate lobectomy can be done safely and effectively.

Keywords: Caudate lobectomy, Surgical flow, Anatomic liver resection

Core tip: Caudate lobe resection is still a challenging procedure for the vast majority of surgeons because of the difficult anatomical location and intraoperative bleeding. According to prior experience, six steps were established and validated on the patient. Anatomic isolated caudate lobectomy can be done safely and effectively following the surgical flow.

INTRODUCTION

The caudate lobe (CL), situated in a tricky location, lies deep in the liver and is adjacent to major blood vessels. CL consists of a Spiegel lobe on the left, a caudate process on the right, and a paracaval portion between them[1]. Surgical resection is the most suitable strategy to eradicate hepatic malignant lesions in this area. In recent years, the number of caudate lobectomies has increased with the improvement of imaging[-5]. However, CL resection remains a challenging procedure for the vast majority of surgeons because of the difficult anatomical location and intraoperative bleeding.

Overall survival (OS) can be achieved by anatomic liver resection for hepatocellular carcinoma (HCC) patients[,]. However, reports of anatomic resection usually refer to segment II to segment VIII, excepting CL. The implement of more CL resection is limited due to a lack of standard flow. Therefore, the aim of this study was to establish the surgical flow for anatomic isolated CL resection.

MATERIALS AND METHODS

Patients

The study was approved by the ethics committee of the Second Affiliated Hospital Zhejiang University School of Medicine. Twenty patients who underwent anatomic isolated caudate lobectomy between April 2004 to July 2014, performed by our group, were enrolled in this study, including 13 males (13/20, 65%) and 7 females (7/20, 35%). The median age of patients was 55.5 years, ranging from 24-72 years. Postoperative pathological examinations included 14 cases of HCC (14/20, 70%), 2 cases of adenocarcinoma (2/20, 10%), 1 case of hepatic hemangioma (1/20, 5%), 1 case of hepatosarcoma (1/20, 5%), 1 case of angioleiomyoma (1/20, 5%), and 1 case of adenoma (1/20, 5%) (Table (Table11).

Table 1

Clinical data for all 20 patients with isolated caudate lobectomy

n = 20Data
Sex
Female7 (35)
Male13 (65)
Age in yr55.5 (24-72)
Pathological examinations
Hepatocellular carcinoma14 (70)
Intrahepatic cholangia carcinoma2 (10)
Hepatic hemangioma1 (5)
Hepatosarcoma1 (5)
Angiomyolipoma1 (5)
Adenoma1 (5)
Tumor size in cm5.5 (2-12)

Surgical approach

The procedures were performed according to the results of computed tomography (CT) or magnetic resonance imaging (MRI) before surgery (Figure (Figure1).1). Based on the location of the tumor, four different flows were planned before surgery (Figure (Figure22).

Magnetic resonance images for caudate lesions. A: T located between PV and IVC; B: Hepatic hemangioma located between RPV and IVC. IVC: Inferior vena cava; PV: Portal vein; RPV: Right portal vein; T: Tumor.

Surgical flow.

Step 1: Mobilization of the liver. For all patients, a reversed L-shaped incision was adopted from xiphoid to the tip of 12th rib. For resection of the caudate process, the right ligamentum teres, falciform ligament, coronary ligament and triangular ligament were divided (Figure (Figure3A).3A). The hepatorenal ligament was dissected and the right adrenal gland was separated from the right liver with a right approach. For resection of the Spiegel lobe, usually, the ligaments of the left liver were dissected, Arantius ligament was divided until the tip of the CL and the Spiegel lobe was exposed completely with a left approach (Figure (Figure4).4). For complete CL resection, usually, both left and right liver were mobilized. For giant CL tumors or the paracaval portion, sometimes, the transection of the liver parenchyma along Cantilie’s line were conducted.

Flow of the caudate lobectomy. A: Liver mobilization; B: Short hepatic veins isolated and divided; C: Three hepatic veins isolated; D: Ischemia landmark of the caudate lobe is shown.

Marking of the left boundary of the caudate lobe. A: Divided Arantius ligament (black arrow); B: Left boundary of caudate lobe (white dotted line).

Step 2: Ligation of short hepatic veins. For a right approach, liver was turned to the left and the inferior vena cava (IVC) was exposed. The inferior right hepatic vein was divided firstly and short hepatic veins were ligated gradually along the IVC (Figure (Figure3B).3B). Vw 2012 tiguan owners manual. The caudate process was exposed and dissociated from the IVC. For a left approach, the liver was turned to the right and short hepatic veins were isolated as well as divided until the Spiegel lobe was separated from the IVC completely.

Step 3: Isolation and taping of three major hepatic veins. The liver was pushed down medially, and the fossa was exposed between the right hepatic vein (RHV) and the middle hepatic vein (MHV) (Figure (Figure3C).3C). A tape was positioned around the common trunk of the MHV and the left hepatic vein (LHV). The hepatocaval ligament (Makuuchi ligament[]) was extra-hepatically dissected from the right side and another tape was positioned around the RHV carefully.

Step 4: Controlling the inflow blood supply. The hepatoduodenal ligament was exposed and a tape was encircled around the hepatic hilum to control hepatic blood inflow if necessary. The occlusion time was usually 5 min, 8 min and 10 min during the first three times and then 10 min with 2 min interruption every time. The branch of portal triads to the CL was divided and ligated. Afterwards, ischemia landmarks could be found easily (Figure (Figure3D3D).

Step 5: Identification of the CL boundary. The left boundary was established as the Arantius ligament, the right boundary was described as Peng’s line from the CL tip to the caudate process[9] (Figure (Figure5).5). The tip of the CL was located between the LHV and the IVC.

Identification of the right boundary of the caudate lobe. Peng’s line was marked as the right boundary, which was from the upper tip to the process (white arc).

Step 6: Liver transection. Hepatic parenchyma was transected with the curettage and aspiration dissection technique using Peng’s multifunction operative dissector[,].

The anatomic isolated caudate lobectomy is presented in the accompanying video (Supplement 1).

Statistical analysis

Clinical variables were described as median or mean ± SD. Discrete and continuous variables were analyzed by chi-square test and t-test, respectively. Survival time was analyzed by the Kaplan-Meier method. All data were analyzed by SPSS 16.0 software (SPSS Inc, Chicago, IL, United States).

RESULTS

Among all patients, 4 cases received isolated complete caudate lobectomy (4/20, 20%), while 16 cases received isolated partial caudate lobectomy (16/20, 80%). Based on the type of dissection, there were 4 cases with the left approach (4/20, 20%), 6 cases with the right approach (6/20, 30%), 7 cases with the bilateral combined approach (7/20, 35%), 3 cases with the anterior approach (3/20, 15%) (Figure (Figure6),6), and the hanging maneuver was also combined in 2 cases. The median tumor size was 5.5 cm (2-12 cm). The median intra-operative blood loss was 600 mL (200-5700 mL). The median intra-operative blood transfusion volume was 250 mL (0-2400 mL). The median operation time was 255 min (110-510 min), and the median post-operative hospital stay was 14 d (7-30 d).

Splitting the liver by the anterior approach. A: The hemangioma was exposed; B: The hemangioma was removed and the major vessels were identified.

There was 1 case of incision infection (1/20, 5%), 3 cases of ascites (3/20, 15%), and 2 cases of pleural effusion (2/20, 10%) (Table (Table2).2). There was no mortality and the median survival time for malignant tumor was 48 mo, with 1- and 3-year survival rates of 88.9% and 49.4%, respectively.

Table 2

Surgical data for all 20 patients with isolated caudate lobectomy

Surgical featureData
Approach
LSR4 (20)
RSR6 (30)
CSR7 (35)
AR3 (15)
Procedure
ICCL4 (20)
IPCL16 (80)
Blood loss in mL600 (200-5700)
VIBT in mL250 (0-2400)
Operation time in min255 (110-510)
HSPO in d14 (7-30)
Postoperative complication
Incision infection1 (5)
Ascites3 (15)
Pleural effusion2 (10)

Data are presented as n (%) or median (range). AR:Anterior resection; CSR: Combined sides resection; HSPO: Hospital stay post operation ; ICCL: Isolated complete caudate lobectomy; IPCL: Isolated partial caudate lobectomy; LSR: Left side resection; RSR: Right side resection; VIBT: Volume of intraoperative blood transfusion.

DISCUSSION

Due to abundant adjacent blood vessels of the CL, chemoembolization, radiofrequency ablation and other treatments are not appropriate for CL lesions[]. Surgical resection is considered as the preferred method and anatomic resection can improve prognosis[,]. Hasegawa et al[] believed that anatomic resection was one of the independent predictors of improved OS for HCC. However, the majority of anatomic resection refers to the segment II to segment VIII, excepting segment I. Caudate lobectomy was once called a ‘bloody gultch’[]. While the resection of the tumor in the CL is not difficult today, it is still difficult to perform isolated anatomic resection for CL; the vast majority reports are from case reports. In this study, we mainly explored the possibility to establish a standard surgical flow for anatomical isolated caudate lobectomy[5,].

Chaib et al[] classified CL tumors into five types, depending on their locations, and this classification has clinical significance for small size tumors. However, in China, HCC is usually large and concurrent with cirrhosis. And, anatomic resection is necessary for longer survival. Blumgart’s group[] performed 150 cases of caudate resection, which led to a median survival for HCC of 32 mo. In 2013, Philips et al[] reported their experience of caudate resection, having a median OS of 21 mo. Our results showed a median survival time of 48 mo for malignant patients, though this was not a comparison study.

Like other anatomic resections, the identification of the blood supply to one part or the whole CL is a prerequisite. The key steps are preoperative assessment and intra-operative identification of the precise boundary. We called this boundary as two tips, two boundaries and one virtual plane. The confluence of Arantius ligament and IVC was the upper tip, while the converging point of the right lobe and the caudate process was the lower tip. The Arantius ligament is regarded as the left border of CL, while Peng’s line is the right border. The plane of the retro-CL is the surface of the retro-hepatic IVC. In practice, resection of the CL along the Peng’s line shows similar effects as intra-operative dye labeling, which is safe and convenient[5].

The advantages of the different surgical approaches are to perform CL resection easily. Left approach is suitable for the tumor located in the Spiegel lobe. Right approach is for resection of tumor located in the caudate process. For complete CL resection, we usually used the left and right approach. For giant CL tumors or the paracaval portion, the anterior approach should be used. The disadvantage of the anterior approach is that incidence of biliary fistula will be high because of hepatic parenchyma transection. The laparoscopic resection of the CL has been reported sporadically, and we will be working on this in the future.

During the resection, other surgical techniques can be used to reduce bleeding and increase surgical safety. These techniques include the selective control of inflow, the liver hanging maneuver and retrograde resection of the CL[,].

In conclusion, as an individual anatomic segment, caudate lobectomy remains a substantially challenging procedure. Our experience demonstrated that anatomic isolated caudate lobectomy can be done safely and effectively by establishing a surgical flow.

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COMMENTS

Background

Caudate lobe (CL) is an important part of the liver and adjacent to the major blood vessels. Surgical resection is the preferred treatment for patients with malignant lesions in this area. However, CL resection remains a challenging procedure.

Research frontiers

The implementation of more CL resections is limited due to a lack of standard flow. The hotspot of this study is the establishment a standard surgical flow for anatomic isolated caudate lobectomy.

Innovations and breakthroughs

In recent years, the number of caudate lobectomies has increased. However, anatomic isolated caudate lobectomy is not common because of the difficult anatomical location and intraoperative bleeding. This study presents the recommendation of a surgical flow which facilitates the performance of anatomic isolated caudate lobectomy safely.

Applications

The surgical flow in this study was established according to prior experience and validated on the patient. Anatomic isolated caudate lobectomy can be done safely and effectively based on this flow.

Terminology

Peng’s line is the right boundary of CL, from the CL tip to the right border of the caudate process. Peng’s multifunction operative dissector is an electrosurgical instrument, which was used for transection hepatic parenchyma.

Peer-review

CL isolated resection is a rare and challenging procedure. I think that the strength of the paper is the description of the different techniques, detailed with intraoperative pictures. The authors deserve praise for having done a difficult job - the article has described a series of 20 resections in a decade. It may be expected that the authors will come up with a larger series in future. The description of operative steps is one of the strong points of this article.

Footnotes

Manuscript source: Unsolicited manuscript

Specialty type: Gastroenterology and hepatology

Country of origin: China

Peer-review report classification

Grade A (Excellent): A, A

Grade B (Very good): B

Grade C (Good): 0

Grade D (Fair): 0

Grade E (Poor): 0

Supported by the National Natural Science Foundation of China, No. 81570559 and No. 81272673; 2014 Zhejiang Provincial Program for the Cultivation of High-level Innovative Health Talents.

Institutional review board statement: The study was reviewed and approved by the Second Affiliated Hospital Zhejiang University School of Medicine Institutional Review Board.

Informed consent statement: All study participants, or their legal guardian, provided informed written consent prior to study enrollment.

Conflict-of-interest statement: We declare that we have no conflict of interest related to this work.

Data sharing statement: Technical appendix, statistical code, and dataset available from the Jiang-Tao Li at zrljt@zju.edu.cn.

Peer-review started: July 5, 2017

First decision: July 28, 2017

Article in press: September 13, 2017

P- Reviewer: Bandyopadhyay SK, Garcia-Olmo D, Petrucciani N S- Editor: Qi Y L- Editor: Filipodia E- Editor: Huang Y

Contributor Information

Yun Jin, Department of General Surgery, The Second Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou 310009, Zhejiang Province, China.

Liang Wang, Department of General Surgery, The Second Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou 310009, Zhejiang Province, China.

Yuan-Quan Yu, Department of General Surgery, The Second Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou 310009, Zhejiang Province, China.

Dong-Er Zhou, Department of General Surgery, The Second Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou 310009, Zhejiang Province, China.

Da-Ren Liu, Department of General Surgery, The Second Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou 310009, Zhejiang Province, China.

Jun-Jie Yang, Department of General Surgery, Xinchang People’s Hospital, Shaoxing 312500, Zhejiang Province, China.

Shu-You Peng, Department of General Surgery, The Second Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou 310009, Zhejiang Province, China.

Jiang-Tao Li, Department of General Surgery, The Second Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou 310009, Zhejiang Province, China. nc.ude.ujz@tjlrz.

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