- Case Report
- Open Access
Acute median arcuate ligament syndrome after pancreaticoduodenectomy
Surgical Case Reportsvolume 2, Article number: 113 (2016)
Median arcuate ligament syndrome (MALS) has been reported in 2–7.6 % of patients undergoing pancreaticoduodenectomy (PD). Most of the reported cases of MALS have been diagnosed perioperatively and treated radiologically or surgically before or during PD. MALS can have an acute postoperative onset after PD even if all preoperative and intraoperative evaluations are normal particularly in young patients.
In this report, we present a second case of severe hepatic cytolysis secondary to MALS that developed acutely and the first patient who required acute division of the median arcuate ligament after PD.
The incidence of celiac axis stenosis (CAS) caused mainly by median arcuate ligament syndrome (MALS) is reported around 7.3 % in asymptomatic individuals . MALS has been reported in 2–7.6 % of patients undergoing pancreaticoduodenectomy (PD) [2–5].
The mechanism of MALS has been well demonstrated. The median arcuate ligament is a tendinous band spanning the right and left diaphragmatic crura, anterior to the aorta. In MALS, the celiac artery (CA) is compressed by this fibrous band, causing extrinsic compression anteriorly and leading to partial or complete CA occlusion [2, 6].
It is crucial to diagnose MALS in the preoperative period when planning PD. The pancreaticoduodenal arcades represent the largest collateral circle to allow retrograde flow through the gastroduodenal artery (GDA) when CAS occurs; this retrograde flow allows for blood to supply the liver, stomach, spleen, and pancreas . Breakdown of this collateral systems during PD in a patient with MALS will cause ischemia of the liver and anastomotic failure [8, 9].
Most of the reported cases of MALS have been diagnosed perioperatively, either by radiologic findings or by intraoperative digital palpation or Doppler sonography [2, 8–10]. When MALS is diagnosed preoperatively, it can be treated by interventional radiology or intraoperatively by median arcuate ligament division or by pass grafting [8, 9, 11–16]. Even when diagnosed perioperatively, MALS can cause severe complications and even mortality after division of the median arcuate ligament or reconstruction of the CA [3, 11, 12, 17–20].
Acute onset MALS during or after PD is very rare. Unfortunately, acute MALS can develop after PD in patient without any radiologic signs of MALS. Sanchez et al.  reported the first patient diagnosed with MALS 1 day after PD in 2013. Although they were able to treat their patient conservatively, there is no standardized approach to this situation.
In this report, we present a patient with MALS that developed acutely after PD, caused severe hepatic cytolysis, and required acute division of the median arcuate ligament.
A 40-year-old male presented to our hospital with a 2-month history of back pain. Physical examination showed no abnormalities, and laboratory examination was normal other than an elevated amylase level. Abdominal contrast-enhanced computed tomography (CT) revealed a low-density mass with a diameter of 20 mm at the pancreatic head, with segmental portal vein (PV) attachment. Endoscopic ultrasonography was performed, and a fine-needle biopsy sample showed adenocarcinoma of the pancreas. Diagnostic laparoscopy ruled out latent peritoneal or liver metastasis. The patient received neoadjuvant chemoradiotherapy (NACRT) using oral fluoropyrimidine (S-1) for 28 days. Post-NACRT CT showed no change in tumor size or in PV attachment.
The patient then underwent PD; intraoperative exploration showed normal anatomy of the celiac trunk, mesenteric vessels, and related branches. Clamp testing of the GDA showed normal hepatic artery pulsation. We performed PD with PV resection and reconstruction and extended lymphadenectomy, including lymph-node dissection around the celiac trunk. Before closing the abdomen, we noted that pulsation of the common hepatic artery became weak, but blood regurgitation was of adequate strength after reopening the cut stump of the right gastric artery. The duration of surgery was 486 min, and the blood loss was 747 mL; blood transfusion was not required. On postoperative day 1, the patient was in stable condition but his liver function tests were abnormal. The preoperative liver enzymes, international normalized ratio (INR), complete blood-cell count (CBC), and tumor markers had all been normal. However, within 12 h of PD, the liver enzymes, INR, white blood cell (WBC) count, platelet (PLT) count, and C-reactive protein (CRP) were abnormal and rapidly worsened over the next 12 h (Table 1).
Although the preoperative CT with routine arterial reconstruction had shown normal CA anatomy and no evidence of MALS, a postoperative scan 1 day after the PD that included a lateral projection of the CA showed an acute extrinsic stenosis caused by newly developed compression caused by the median arcuate ligament. Widespread liver ischemia was also apparent (Figs. 1, 2, and 3).
The patient underwent urgent reoperation for acute onset MALS causing severe hepatic cytolysis. There was no palpable blood flow at the celiac trunk, and flow at the hepatic artery was markedly decreased. Bile leakage from the suture points of the hepaticojejunostomy was detected; this seemed to be caused by decreased blood flow in the common hepatic artery. The median arcuate ligament was released, with subsequent dramatic resumption of celiac trunk and common hepatic artery hepatic artery pulsation.
After division of the median arcuate ligament, the patient’s liver enzymes, INR, and WBC gradually normalized. Eleven days after reoperation, CT showed regular flow into the celiac trunk, the proper hepatic artery, and the PV; the area of liver ischemia was reduced (Figs. 4 and 5). The patient did not experience any regurgitant cholangitis and liver abscess. Prompt MALS release was succesful in order to prevent any major complications. The patient required a longer than usual postoperative stay in order to recover from bile leakage. He was eventually discharged 43 days after the original PD, in good condition.
The pancreaticoduodenal arcades make up the major collateral circle that allows retrograde flow through the GDA in case of CAS. They allow for blood to reach the hepatic, gastric, splenic, and pancreatic arteries when the celiac trunk is compromised .
The preoperative diagnosis of MALS is essential so that this arcade may be preserved [8, 9]. It is not always possible to diagnose MALS before proceeding with pancreatic resection during PD. Failure to demonsrate MALS before or during PD could potentially cause major morbidity, leading to ischemic and fatal complications [11, 17–19].
Three-dimensional CT angiography shows a characteristic hook pattern on the anterior proximal celiac axis when it is compressed by the median arcuate ligament [13, 14]. Gaujoux et al.  reported that multidetector CT, including lateral views, can detect significant arterial stenosis with 96 % sensitivity and determine the etiology of CA stenosis with 92 % accuracy.
If MALS is diagnosed before PD, various methods are available for revascularization before or during the procedure: these include open or laparoscopic median arcuate ligament division, a vascular bypass procedure, or endovascular stenting [16–18, 21–25].
Intraoperative trial clamping of the GDA should be performed before breakdown of the collateral circulation during PD, even if preoperative CT does not demonstrate MALS . If MALS is present, this clamping will markedly decrease the hepatic artery pulsation as evaluated by digital palpation or intraoperative Doppler ultrasonography . If MALS is diagnosed during PD, the median arcuate ligament must be divided at the beginning of the procedure, before GDA ligation or pancreatic division [15, 20]. This safe and fast procedure permits trunk decompression and resolution of ischemic disorders in up to 89 % of patients .
MALS can develop acutely after PD in patients with normal hepatic artery flow during GDA clamping. Sanchez et al.  reported the first patient with acute onset MALS after PD who did not demonstrate hepatic artery flow impairment during GDA clamping. They were able to treat their patient conservatively. We report herein a second such patient who had no evidence of hepatic artery flow impairment during GDA clamping and pancreatic transection.
Since the appearance of MALS after PD is very rare, the appropriate treatment has to be determined according to the patient’s general status. We decided on exploratory laparotomy since our patient had abundant hepatic cytolysis. Also influencing our decision, his liver enzymes, INR, and CRP worsened abruptly within 12 h of the original surgery and rapidly increased by 24 h after PD. Repeat CT also showed widespread liver ischemia. At re-exploration, we noted bile leakage from the suture points of the hepaticojejunostomy, probably due to the decreased blood flow from the common hepatic artery. Eventually, our patient developed a biliary fistula that required extended hospitalization.
There is no known explanation for this acute onset of MALS after PD in a patient with normal celiac anatomy. Sanchez et al.  tried to explain this phenomenon as occurring in patients with pre-existing nonsignificant CAS that is exacerbated by either extended lymphadenectomy of the celiac region or by the prolonged bent back position of the patient during surgery. However, our patient’s celiac lymphadenectomy and duration of the surgery were not different from our other patients who have not developed MALS. Although our patient underwent NACRT followed by PD, the field of radiation did not include the region of the celiac trunk. We hypothesize that a very tight median arcuate ligament presented in this young patient in addition to lymph-node clearance around the celiac trunk might induce the stenosis.
MALS is most often diagnosed preoperatively, and a small portion of patients are diagnosed intraoperatively. Unfortunately as in our patient, MALS can have an acute postoperative onset even if all preoperative and intraoperative evaluations are normal. Hepatic cytolysis after PD with extended lymphadenectomy should alert clinicians to the possibility of MALS, even in patients with normal radiological vascular anatomy. Patients who acutely deteriorate despite medical treatment should undergo surgical exploration to rule out other conditions and division of the median arcuate ligament in order to prevent any major complications if MALS is indeed present.
Celiac axis stenosis
Complete blood-cell count
International normalized ratio
Median arcuate ligament syndrome
White blood cell
Park CM, Chung JW, Kim HB, Shin SJ, Park JH. Celiac axis stenosis: incidence and etiologies in asymptomatic individuals. Korean J Radiol. 2001;2:8–13.
Farma JM, Hoffman JP. Nonneoplastic celiac axis occlusion in patients undergoing pancreaticoduodenectomy. Am J Surg. 2007;193:341–4.
Berney T, Pretre R, Chassot G, Morel P. The role of revascularisation in celiac occlusion and pancreatoduodenectomy. Am J Surg. 1998;176:352–6.
Pfeiffenberger J, Adam U, Drognitz O, Kröger JC, Makowiec F, Schareck W, et al. Celiac axis stenosis in pancreatic head resection for chronic pancreatitis. Langenbecks Arch Surg. 2002;387:210–5.
Trede M. The surgical treatment of pancreatic carcinoma. Surgery. 1985;97:28–35.
Kim SJ, Park YJ, Yang SS, Kim YW. Open surgical decompression of celiac axis compression by division of the median arcuate ligament. J Korean Surg Soc. 2013;85:93–5.
Sanchez AM, Alfieri S, Caprino P, Tortorelli AP, Doglietto GB. Temporary medium arcuate ligament syndrome after pancreatoduodenectomy. Am Surg. 2013;79:E58–60.
Kurosaki I, Hatakeyama K, Nihei KE, Oyamatsu M. Celiac axis stenosis in pancreaticoduodenectomy. J Hepatobiliary Pancreat Surg. 2004;11:119–24.
Nakano H, Yamamura T, Yamaguchi S, Otsubo T. Celiac axisocclusion of a patient undergoing pancreaticoduodenectomy after distal gastrectomy. Hepatogastroenterology. 2007;54:595–8.
Halazun KJ, Kotru A, Menon KV, Patel J, Prasad KR. Stenting of coeliac axis stenosis facilitates pancreatectomy. Eur J Surg Oncol. 2006;32:811–2.
Celik S, Ringe KI, Boru CE, Constantinica V, Bektas H: A case of pancreatic cancer with concomitant median arcuate ligament syndrome treated successfully using an allograft arterial transposition. J Surg Case Rep. 2015;2015(12):1–4.
Whistance RN, Shah V, Grist ER, Shearman CP, Pearce NW, Odurny A, et al. Management of median arcuate ligament syndrome in patients who require pancreaticoduodenectomy. Ann R Coll Surg Engl. 2011;93:e11–4.
Horton KM, Talamini MA, Fishman EK. Median arcuate ligament syndrome: evaluation with CT angiography. Radiographics. 2005;25:1177–82.
Foertsch T, Koch A, Singer H, Lang W. Celiac trunk compression syndrome requiring surgery in 3 adolescent patients. J Pediatr Surg. 2007;42:709–13.
Gaujoux S, Sauvanet A, Vullierme M-P, Cortes A, Dokmak S, Sibert A, et al. Ischemic complications after pancreaticoduodenectomy: incidence, prevention, and management. Ann Surg. 2009;249:111–7.
Fortner JG, Watson RC. Median arcuate ligament obstruction of celiac axis and pancreatic cancer. Ann Surg. 1981;194:698–700.
Bull DA, Hunter GC, Crabtree TG, Bernhard VM, Putnam CW. Hepatic ischemia, caused by celiac axis compression, complicating pancreaticoduodenectomy. Ann Surg. 1993;217:244–7.
Thompson NW, Eckhauser FE, Talpos G, Cho KJ. Pancreaticoduodenectomy and celiac occlusive disease. Ann Surg. 1981;193:399–406.
Biehl TR, Traverso LW, Hauptmann E, Ryan Jr JA. Preoperative visceral angiography alters intraoperative strategy during the Whipple procedure. Am J Surg. 1993;165:607–12.
Winter JM, Cameron JL, Yeo CJ, Alao B, Lillemoe KD, Campbell KA, et al. Biochemical markers predict morbidity and mortality after pancreaticoduodenectomy. J Am Coll Surg. 2007;204:1029–36.
Dordoni L, Tshomba Y, Giacomelli M, Jannello AM, Chiesa R. Celiac artery compression syndrome: successful laparoscopic treatment—a case report. Vasc Endovascular Surg. 2002;36:317–21.
Roayaie S, Jossart G, Gitlitz D, Lamparello P, Hollier L, Gagner M. Laparoscopic release of celiac artery compression syndrome facilitated by laparoscopic ultrasound scanning to confirm restoration of flow. J Vasc Surg. 2000;32:814–7.
Jarry J, Berard X, Ducasse E, Biscay D, Pailler A, Sassoust G, et al. [Laparoscopic management of median arcuate ligament syndrome] (article in French). J Mal Vasc. 2008;33:30–4.
Weber JM, Boules M, Fong K, Abraham B, Bena J, El-Hayek K, et al. Median arcuate ligament syndrome is not a vascular disease. Ann Vasc Surg. 2016;30:22–7.
Jimenez JC, Harlander-Locke M, Dutson EP. Open and laparoscopic treatment of median arcuate ligament syndrome. J Vasc Surg. 2012;56:869–73.
All authors conceived of the study and participated in its design and coordination and helped to draft the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Written informed consent was obtained from the patient for the publication of this case report and accompanying images. A copy of the written consent is available for review by the editor-in-chief of the journal.