Abstract
Laparoscopically harvested left liver (LL) grafts have drawbacks with respect to the size and shape of graft hepatic vein orifices. We present two cases of pediatric living donor liver transplantation (LDLT) using laparoscopically harvested LL grafts and describe refined surgical techniques for graft hepatic vein venoplasty. The first case was a boy aged 4 years and 5 months, with hepatoblastoma. The donor was his 35-year-old mother, and LL graft weighed 315 g. Two separate openings of the graft at the left hepatic vein (LHV) and middle hepatic vein (MHV) were unified through septotomy and septoplasty, and cryopreserved vein homograft patch was attached. Standard procedures of LDLT were performed. This patient recovered uneventfully and has been doing well for 4 years without tumor recurrence. The second case was a 6-year-old girl with ornithine transcarbamylase deficiency. The donor was her 35-year-old mother, and the LL graft weighed 310 g. Two separate openings of graft MHV, with segment III and segment II veins, were unified through septoplasty, and vein patch was attached. Standard procedures of LDLT were performed. This patient has been doing well for 4 years. In conclusion, separate graft hepatic vein openings are a drawback of laparoscopically harvested LL grafts, which thus require unification venoplasty of customized design individually tailored for LL graft and pediatric recipient.
Living donor hepatectomy performed using total laparoscopy has definite merit for the cosmetic aspect of the donor’s abdominal wound [1-6]. However, there are drawbacks of the liver grafts, in which the graft hepatic vein stump is very short because it is transected by an endoscopic vascular stapler, and the stapled stump of the graft side should be excised. Therefore, such condition often makes the graft hepatic vein orifice unsuitable for direct anastomosis.
A left liver (LL) graft used for living donor liver transplantation (LDLT) has two outflow veins, the left hepatic vein (LHV) and middle hepatic vein (MHV). In the LL grafts harvested through open surgery, the shapes of the graft outflow vein orifices appear to be a single orifice or similar to a figure of 8; thus, they require only a simple venoplasty. In contrast, in the LL grafts harvested through laparoscopic surgery, the stumps of the LHV and MHV are usually completely separate [5]; therefore, complex unification venoplasty is recommended and necessary to achieve best results. The surgical technique of unification venoplasty for laparoscopically harvested LL grafts is different from that for laparoscopically harvested left lateral section grafts. We herein present two cases of pediatric LDLT using a laparoscopically harvested LL graft and describe the refined surgical techniques for unification of LHV and MHV orifices.
This study, a retrospective review, was approved by the Institutional Review Board of Asan Medical Center (IRB No. 2020-0836). Owing to the retrospective design, the requirement for informed consent was waived.
The patient was a boy aged 4 years and 5 months with previously diagnosed hepatoblastoma. The tumor was shown to be a hepatoblastoma of the epithelial type as seen on a percutaneous liver biopsy (Fig. 1A) and classified as a pretreatment extent of disease (PRETEXT) stage IV tumor. After five cycles of systemic chemotherapy, the hepatic tumor was markedly reduced in size and number (Fig. 1B), and there was no evidence of distant metastasis on fluorodeoxyglucose-positron emission tomography (Fig. 1C). Thus, LDLT was planned to treat the residual tumors. At LDLT operation, the patient’s height was 105 cm and weight was 17 kg.
The donor in this case was the patient’s 35-year-old mother. Computed tomography (CT) volumetry showed that the estimated volume of the left hemiliver was 340 mL (Fig. 2). The LL graft was harvested using a totally laparoscopic approach and delivered through a suprapubic incision. The detailed procedures of the totally laparoscopic LL graft harvest have been presented in a previous report [5]. The LL graft weighed 315 g, with a graft-recipient weight ratio (GRWR) of 2.6%. There were two separate openings (LHV and MHV) in the graft (Fig. 3A and B). The intervening hepatic parenchyma between these openings was excised through a septotomy (Fig. 3C and D), and then a unification septoplasty was performed (Fig. 3E). Next, a small superficial branch of the LHV was opened, and unification suture was performed to widen the orifice further. Then, an incision was made at the medial wall of the MHV trunk, and a patch of cryopreserved external iliac vein homograft was attached (Fig. 3F and G), which made the graft outflow vein orifice 4 cm in transverse diameter (Fig. 3H).
Recipient hepatectomy was performed according to standard procedures. After total clamping of the inferior vena cava (IVC), the hepatic parenchyma was incised using a surgical knife, leaving the bulk of the hepatic parenchyma around the hepatic vein trunks. After the native liver was taken out, the attached hepatic parenchyma was forcefully pulled out to detach it from the hepatic vein stumps, which made the hepatic vein stump walls long and thick. The IVC wall septa between the right hepatic vein and MHV and the MHV and LHV were consecutively transected to form a single large hepatic vein orifice. The transverse diameter of this unified hepatic vein orifice was approximately 4 cm. At the initiation of the graft implantation, we tagged the right and left corners of the graft and the recipient’s hepatic vein orifices with 5–0 polydioxanone (PDS) to match their sizes. Then, we performed continuous sutures of the posterior wall continued first from the left corner in the 6 o’clock direction, and then the suturing continued toward the right corner after meticulous size matching. Continuous running suturing continued to the anastomosis of the anterior wall. After injecting heparinized saline into the IVC lumen, we completed the graft hepatic vein reconstruction. Thereafter, the branch patch of the recipient’s portal vein was stretched toward the graft portal vein, and continuous suturing with a 6–0 PDS was performed for portal vein reconstruction. The graft left hepatic artery was anastomosed with the recipient’s left hepatic artery branch under surgical microscopy. Hepaticojejunostomy using a Roux-en-Y jejunal limb was performed for biliary reconstruction.
The pathology report revealed that the multiple residual hepatoblastomas were epithelial type with fetal subtypes with sizes up to 4.5 cm. Tumor necrosis of 70% without microvascular invasion and lymph node metastasis was detected (Fig. 1D). This patient recovered uneventfully without any surgical complication (Fig. 4A-C). He has been doing well for 4 years to date without any sign of tumor recurrence (Fig. 4D).
The patient was a 6-year-old girl who suffered from ornithine transcarbamylase (OTC) deficiency (Fig. 5A). This disorder was diagnosed using OTC gene sequencing, in which the nucleotide mutation included c.–441A>G and c.–359G>A. The patient was frequently in a lethargic state and vomiting, with a noted elevation in blood ammonia levels. She also had been diagnosed with Duchenne muscular dystrophy. Thus, we planned to perform LDLT. At the LDLT operation, the patient’s height and weight were 109 cm and 17 kg, respectively. One day before the LDLT operation, continuous renal replacement therapy was initiated to control the symptoms of OTC deficiency.
The donor was the patient’s 35-year-old mother. CT volumetry showed that the estimated volume of the left hemiliver was 330 mL (Fig. 6). The LL graft was harvested by a total laparoscopic approach and delivered through the suprapubic incision. The LL graft weighed 310 g, with a GRWR of 1.8%. There were two separate openings of the MHV, with segment III and segment II veins at the graft (Fig. 7A and B). A unification septoplasty was performed (Fig. 7C). For this procedure, an incision was made at the medial wall of the MHV trunk and a cryopreserved vein patch homograft was attached (Fig. 7D), which made the graft outflow vein orifice 4 cm in transverse diameter.
The recipient hepatectomy was performed according to standard procedure. The procedures for graft implantation were the same in the abovementioned case, except for biliary reconstruction through duct-to-duct anastomosis. The pathology report presented that there was diffuse glycogenesis with moderate fatty change and perivenular fibrosis, which was consistent with OTC deficiency (Fig. 5B). Notably, after LDLT, it was shown that right pleural effusion developed; thus, a percutaneous drainage was performed. This patient experienced acute cellular rejection (rejection activity index, 3) at 2 weeks after transplantation and recovered with augmentation of immunosuppression. On the early posttransplant CT image, the site of graft hepatic vein reconstruction appeared to be compressed (Fig. 8A and B), but such a configuration was normalized after resolution of acute cellular rejection and loss of pleural effusion (Fig. 8C and D). At 4 months after transplantation, biliary stricture developed at the anastomosis site, which was successfully treated with an endoscopic retrograde biliary drainage tube and using a retrievable metallic wall stent. The patient has been doing well for 4 years to date.
Pediatric LDLT is vulnerable to vascular complications primarily because the graft and recipient vessels are smaller than in adult LDLT; thus, surgical techniques ensuring secure vascular reconstruction should be used in these cases. Regarding graft hepatic vein reconstruction, making the graft hepatic vein suitable for anastomosis on the back table is the most effective method to prevent hepatic vein outflow obstruction. We have developed various surgical techniques of hepatic vein venoplasty for various types of partial liver grafts [7-10].
Compared with the usual LL grafts harvested through an open surgery, those harvested through a laparoscopic approach have a definite drawback in the graft hepatic vein. It is noted that a laparoscopically harvested LL graft usually has separate openings for the LHV and MHV trunks, as shown in our two cases. The common LHV-MHV trunk of the donor is stapled at the donor and graft sides using an endoscopic vascular stapler, and the stapled stump at the graft should be excised to drain the graft hepatic vein orifice [5]. This process results in an additional removal of the graft hepatic vein stump, compared with open surgery. Since such a hepatic vein orifice of a LL graft is not suitable for direct anastomosis, a customized hepatic vein that is individually designed for the graft and recipient is necessary to perform secure outflow vein reconstruction.
For designing hepatic vein venoplasty for a LL graft, several graft and recipient factors should be taken into account. First, the size of the recipient hepatic vein orifice at the IVC should be assessed before any design could be made in the case. It is not possible to measure the size before removal of the recipient’s native liver, but there are ways to empirically estimate the size of the recipient hepatic vein orifice. For pediatric patients weighing around 20 kg, similar to our cases, the stretched transverse diameter of a recipient hepatic vein orifice is usually 4 cm. In contrast, it is often increased to 5 cm in adolescent and adult recipients. The second factor for consideration is the GRWR. If the GRWR exceeds 2% in pediatric patients older than 3 years of age, we intentionally remove the intervening liver parenchyma between the LHV and MHV to form a common channel at the graft hepatic vein orifice, which is beneficial to tolerate the extrinsic graft compression by accommodation of a large-sized graft. The third factor is the shape and size of the separate graft hepatic vein openings. Various techniques are used for unification of these hepatic vein orifices, including the procedures of simple unification, unification after septotomy, and unification after septotomy and parenchymal excision. The fourth factor is availability of the vein homograft. The medial wall of the MHV trunk at a laparoscopically harvested LL graft is usually short and weak, a condition not suitable for direct anastomosis. Likewise, attachment of a vein patch makes the medial wall of the MHV trunk suitable for suturing. The size of a vein patch is dependent on the required target diameter of the graft hepatic vein orifice, which is a requirement for one-to-one matching with the recipient hepatic vein orifice. These four components were integrated in the design of the graft hepatic vein venoplasty in our cases.
A superficial branch of the LHV is identified in a considerable proportion of LL or left lateral section grafts [11,12]. Although this vein is small, it can be used for venoplasty, by which the actual cross-sectional area of the LHV anastomosis can be slightly increased, as shown in our case No. 1. Based on our experience, any superficial branch of the LHV regardless of size can be effectively used for unification venoplasty.
Any vein patch can be used for a patch venoplasty of the graft hepatic vein orifice. If necessary, the living donor’s gonadal or ovarian vein can be harvested because the pediatric recipient’s veins are too small to use for venoplasty. If a vein homograft is available, it is the best material for making a sizable vein patch. Currently, cryopreserved femoral vein and artery homografts are available through the Korea Public Tissue Bank. The cryopreserved external iliac vein homografts used in our cases were obtained from the institutional tissue bank of our institution. All human tissues stored at the tissue bank were donated after informed consent was provided by the donor’s family members. All procedures for vascular tissue procurement and processing were performed in compliance with Korean legislation and, therefore, conformed to the ethical and safety concerns for therapeutic use [13].
In conclusion, the laparoscopically harvested LL grafts has a drawback of widely separate graft hepatic vein openings; thus, a unification venoplasty of customized design individually tailored for the LL graft and pediatric recipient is required to ensure a secure graft hepatic vein reconstruction.
Notes
Conflict of Interest
Shin Hwang is an editorial board member of the journal but did not involve in the peer reviewer selection, evaluation, or decision process of this article. No other potential conflicts of interest relevant to this article were reported.
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