Pancreatic head carcinoma and right hepatic artery: embolization management—A case report
Case Report

Pancreatic head carcinoma and right hepatic artery: embolization management—A case report

Mehdi El amrani1, Emmanuelle Leteurtre2, Géraldine Sergent3, Olivier Ernst3, Vincent Maunoury4, Julien Branche4, François-René Pruvot1, Stéphanie Truant1

1Department of Gastrointestinal Surgery and Transplantation, Lille University and Hospital, France; 2Department of Pathology, 3Department of Radiology, 4Gastroenterology Unit, Hôpital Huriez, Lille University and Hospital, France

Correspondence to: Mehdi El amrani, MD. Department of Gastrointestinal Surgery and Transplantation, Hôpital Claude Huriez, Rue Michel Polonovski, 59037 Lille Cedex, France. Email: Mehdi_elamrani@hotmail.fr or mehdi.elamrani@etu.univ-lille2.fr.

Abstract: A replaced right hepatic artery (RHA) is the most common anatomical variation in pancreatic surgery. The RHA is frequently encountered and can be problematic in pancreatic carcinoma. The preservation of the RHA is necessary to avoid ischemic complications but can impact margins resection in pancreaticoduodenectomy (PD). We report a case of a 53-year-old man with a head pancreatic carcinoma. There was a close contact between the tumor and the RHA arising from superior mesenteric artery (SMA). Preoperative embolization of the RHA was performed prior to PD.

Keywords: Pancraticoduodenectomy (PD); right hepatic artery (RHA); embolization; pancreatic head carcinoma


Submitted May 30, 2014. Accepted for publication Jun 10, 2014.

doi: 10.3978/j.issn.2078-6891.2014.040


Introduction

An aberrant hepatic artery is a common anatomical variant (1). The right hepatic artery (RHA) arising from the superior mesenteric artery (SMA), is frequently encountered and can be problematic in pancreatic ductal adenocarcinoma (PDAC) (2). Pancreaticoduodenectomy (PD) is the intervention of choice in periampullary carcinoma. The preservation of the RHA is necessary to avoid ischemic complications but can impact margins resection. Another option consisting in arterial resection followed by reconstruction is possible but is known to increase complication rates. We reported a case of preoperative embolization of the RHA in a patient with pancreatic head tumor. That embolization allowed the development of collaterals from the left branch of the hepatic artery to the right liver lobe.


Case report

A 53-year-old man, with history of ischemic heart disease, arterial hypertension and alcohol intoxication presented altered general status with weight loss and jaundice since one month. The blood analysis showed cholestasis (total bilirubin =125 mg/L) and cytolysis [aspartate aminotransferase (ASAT) =258 UI/L, alanine aminotransferase (ALAT) =625 UI/L]. The serum carbohydrate antigen level (CA19-9) was slightly increased at 50.9 U/mL while carcinoembryonic antigen (CEA) level was normal at 2.6 µg/L.

The abdominal computed tomography (CT) revealed a 16 mm × 18 mm mass of the pancreas head coming in contact with the underside of the portal vein but with no abutment or invasion of the superior mesenteric vessels. There was a 12 mm retro-portal lymph node, with no distant metastasis. The left branch of the hepatic artery had a regular origin from the middle hepatic artery, whereas there was a RHA arising from the SMA that was exclusive for the right liver lobe (i.e., replaced RHA Michels 3) (3). There was a close contact between the tumor and the RHA (Figure 1). The complementary investigations were also negative. Embolization of this artery was carried out by percutaneous puncture of the right femoral artery. After catheterization of the RHA, we set up a plug of 7 mm of diameter obtaining immediately the complete obstruction of the RHA (Figure 2). A concomitant biliary drainage had been previously performed to reduce jaundice and avoid septic complications.

Figure 1 Preoperative CT scan of patient showed a right hepatic artery (arrow) arising from the superior mesenteric artery (arrowhead) and passing in close contact with the tumor. CT, computed tomography.
Figure 2 (A) Angiography of patient after selective catheterization shows a RHA arising from SMA; (B) obstructed RHA after embolization by plug. RHA, right hepatic artery.

A CT was done on the first postembolization day and after three weeks. The first CT revealed total obstruction of the RHA with subsequent right hepatic ischemia. The second CT demonstrated the disappearance of the right hepatic ischemia and the development of a collateral system arising from the left branch and revascularizing the right liver lobe (Figure 3).

Figure 3 (A) Right hepatic ischemia (asterisk) observed on the CT performed on the first day following embolization; (B-D) a follow-up CT carried out three weeks after embolization demonstrated the development of a collateral system arising from the left branch and revascularizing the right liver lobe (arrow), and postembolization RHA by a plug (headarrow). RHA, right hepatic artery; CT, computed tomography.

The patient was operated 22 days after the embolization. After an abdominal exploration, PD was performed. The liver parenchyma did not show any signs of ischemia. There was a macroscopic invasion of both the portal vein and the RHA requiring a monobloc resection. After segmental resection, the portal vein was reconstructed through an end-to-end anastomosis. The complete retro-portal lamina excision was particularly difficult due to inflammation caused by embolization. The histopathological examination of the specimen revealed a pancreatic duct adenocarcinoma with 3 metastatic lymph nodes out of 15 resected. The RHA was not microscopically invaded but located at 0.5 mm from the tumor edge. All margins, especially the vascular one, were negative.


Discussion

The hepatic arterial vasculature is extremely variable (1). In most cases, the hepatic artery arises from the celiac axis, dividing into two branches destinated to both hepatic lobes (3,4). However, anatomical variants are observed in up to 30% to 46% of patients (1,3). A replaced RHA is one of the most common anatomical variant. It takes origin from the SMA and access to the hepatic pedicle by following the retroportal lamina behind the head of pancreas. Michels reported a classification of anatomic variation of hepatic artery supply in 1966 (3). In 200 specimens, 26% of aberrant RHA were encountered, of which 18% were replaced and 8% were accessory. The exact knowledge of this variant by surgeons is required to prevent a vascular injury during PD. In fact, the vascularization of the common bile duct is provided by both the gastroduodenal artery (GDA) and the right branch of the hepatic artery or the RHA if it’s replaced. In PD, the GDA is ligated and injury or ligation of the RHA can favor ischemic complications and secondary biliary fistula or stenosis (5,6). This arterial interruption can also promote ischemic cholangitis and hepatic abscess in some cases (7). Turrini et al. reported RHA identification by radiologists in preoperative CT in only 30% of patients, while it was detected by surgeons in 50% of cases (4).

Several series have reported the impact of the RHA on PDAC management and outcome. Eshuis et al. described a similar surgical morbidity rate in patients with RHA compared with patients with no arterial variation (8). The presence of RHA in patients with PDAC did not appear to affect resectability in most series (4,9,10). Turrini et al. reported no difference in rates of positive resection margins despite the preservation of a replaced or accessory RHA during PD (4). However, these data were published before standardization of histopathological analysis and could have underestimated the rates of R1 vascular margin (11). When this artery is invaded or in contact with the tumor, its resection is necessary to obtain free resection margins, especially for the vascular margin. This latter is reported as a major predictor of long-term survival following PD for PDAC (11). Some authors reported that RHA ligation with reconstruction is safe and feasible (4,12). The preoperative embolization of RHA is an interesting alternative as it prepares the patient to the intervention by allowing the development of the collaterals from the left branch. In our patient, hepatic ischemia was observed on CT performed 1day after embolization demonstrating the real existence of ischemia and its potential consequences for the patient after PD if the RHA would have been injured or sacrificed without reconstruction. A follow-up CT performed three weeks after embolization demonstrated the development of a collateral system arising from the left branch to the right liver lobe with no residual ischemia. The tumor size remained stable. No adverse effect was reported.

The patient underwent PD three weeks after embolization. The excision of retroportal lamina was especially challenging due to important inflammation caused by the plug in the proximal part of the RHA. We now advise that RHA embolization should be performed at the level of the hepatic pedicle, away of the RHA origin to prevent this inflammation. On the other hand, very distal embolization must be avoided because it may hinder the collaterals development. The histological examination confirmed an R0 resection. To our knowledge, there are only few cases of RHA embolization before PD reported in the literature. Cloyd et al. reported the first description of embolization of RHA in two patients with periampullary tumors (13). Some authors described preoperative embolization of a replaced common hepatic artery arising from the SMA in patients with pancreatic cancer without any serious complications (14,15).

In conclusion, the knowledge of hepatic artery variation is essential in pancreatic surgery. Preoperative embolization of RHA that is exclusive for the vascularization of the right liver lobe can be useful.


Acknowledgements

Disclosure: The authors declare no conflict of interest.


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Cite this article as: El amrani M, Leteurtre E, Sergent G, Ernst O, Maunoury V, Branche J, Pruvot FR, Truant S. Pancreatic head carcinoma and right hepatic artery: embolization management. J Gastrointest Oncol 2014;5(4):E80-E83. doi: 10.3978/j.issn.2078-6891.2014.040

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