Retrospective Study Open Access
Copyright ©The Author(s) 2016. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastrointest Surg. Jun 27, 2016; 8(6): 427-435
Published online Jun 27, 2016. doi: 10.4240/wjgs.v8.i6.427
Impact of previous cyst-enterostomy on patients’ outcome following resection of bile duct cysts
Mehdi Ouaissi, Department of General and Digestive Surgery, La Timone Hospital, 13009 Marseille, France
Reza Kianmanesh, Department of Digestive and Endocrine Surgery, Robert Debré Hospital, 51090 Reims, France
Emilia Ragot, Jacques Belghiti, Department of HPB Surgery, Beaujon Hospital, 92110 Clichy, France
Pietro Majno, Department of Digestive Surgery, Geneva University Hospital, 1205 Geneva, Switzerland
Gennaro Nuzzo, Department of HPB Surgery, Gemelli University Hospital, 00168 Roma, Italy
Remi Dubois, Department of Pediatric Surgery, Mother and Children Hospital, 69677 Bron, France
Yann Revillon, Department of Pediatric Digestive Surgery, Necker Hospital, 75175 Paris, France
Daniel Cherqui, Department of Digestive and HPB Surgery, Paul Brousse Hospital, 94800 Villejuif, France
Daniel Azoulay, Department of Digestive and HPB Surgery, Henri Mondor Hospital, 94000 Creteil, France
Christian Letoublon, Department of Digestive Surgery, Michallon Hospital, 38043 Grenoble, France
François-René Pruvot, Department of Digestive surgery and Transplantation, Claude Huriez Hospital, 59037 Lille, France
François Paye, Department of Digestive Surgery, , 75012 Paris, France
Patrick Rat, Department of Digestive Surgery, Dijon University Hospital, 21000 Dijon, France
Karim Boudjema, Department of HPB Surgery, Pontchaillou Hospital, 35033 Rennes, France
Adeline Roux, Pôle Information Médicale Evaluation Recherche, Unité de Recherche Clinique, 69317 Lyon, France
Jean-Yves Mabrut, Department of Digestive Surgery and Hepatic Transplantation, La Croix-Rousse Hospital, 69317 Lyon, France
Jean-François Gigot, Department of Abdominal Surgery and Transplantation Division of Hepato-Biliary and Pancreatic Surgery Cliniques Universitaires Saint-Luc, 1200 Brussels, Belgium
Author contributions: All the authors contribute to the manuscript.
Institutional review board statement: A multicenter retrospective study was conducted under the auspices of the Association Française de Chirurgie among their members, surgeons coming mainly from European countries. The patients’ medical records were included on a website database (http://www.chirurgie-viscerale.org) using an online computerized standardized questionnaire.
Informed consent statement: A multicenter retrospective study was conducted under the auspices of the Association Française de Chirurgie among their members, surgeons coming mainly from European countries.
Conflict-of-interest statement: All the authors have no conflicts of interest.
Data sharing statement: No data was created, so no data are available.
Open-Access: This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
Correspondence to: Jean-François Gigot, Professor, Department of Abdominal Surgery and Transplantation Division of Hepato-Biliary and Pancreatic Surgery Cliniques Universitaires Saint-Luc, Hippocrate Avenue, 1200 Brussels, Belgium. jean-francois.gigot@uclouvain.be
Telephone: +32-27-641505
Received: December 27, 2015
Peer-review started: January 11, 2016
First decision: February 2, 2016
Revised: March 21, 2016
Accepted: April 7, 2016
Article in press: April 8, 2016
Published online: June 27, 2016

Abstract

AIM: To analyze the impact of previous cyst-enterostomy of patients underwent congenital bile duct cysts (BDC) resection.

METHODS: A multicenter European retrospective study between 1974 and 2011 were conducted by the French Surgical Association. Only Todani subtypes I and IVb were included. Diagnostic imaging studies and operative and pathology reports underwent central revision. Patients with and without a previous history of cyst-enterostomy (CE) were compared.

RESULTS: Among 243 patients with Todani types I and IVb BDC, 16 had undergone previous CE (6.5%). Patients with a prior history of CE experienced a greater incidence of preoperative cholangitis (75% vs 22.9%, P < 0.0001), had more complicated presentations (75% vs 40.5%, P = 0.007), and were more likely to have synchronous biliary cancer (31.3% vs 6.2%, P = 0.004) than patients without a prior CE. Overall morbidity (75% vs 33.5%; P < 0.0008), severe complications (43.8% vs 11.9%; P = 0.0026) and reoperation rates (37.5% vs 8.8%; P = 0.0032) were also significantly greater in patients with previous CE, and their Mayo Risk Score, during a median follow-up of 37.5 mo (range: 4-372 mo) indicated significantly more patients with fair and poor results (46.1% vs 15.6%; P = 0.0136).

CONCLUSION: This is the large series to show that previous CE is associated with poorer short- and long-term results after Todani types I and IVb BDC resection.

Key Words: Bile duct cyst, Congenital, Biliary disease, Cyst-enterostomy, Long-term outcome

Core tip: Previous cyst-enterostomy is associated with more severe clinical presentation, including increased incidence of synchronous cancer, as well as poorer short- and long-term results in patients undergoing operations for Todani types I and IVb bile duct cysts.



INTRODUCTION

In contrast to Asian countries[1], congenital bile duct cysts (BDC) are rare in the United States and in Europe[2] , with an incidence between 1 in 13000 and 1 in 2 million live births[3], respectively. whereas the incidences vary from 1 in 1000 in Japan[4], to 1 in 13500 in United States[5] and 1 in 15000 in Australia[6]. For this reason, there are few published series concerning the Western experience with this disease process[7]. The optimal surgical procedure for the management of BDC is still debated with cyst-enterostomy (CE) having been preferred in the past owing to its technical simplicity[8,9]. However, CE has been reported to be associated with increased morbidity (especially biliary complications) and higher reoperation rates during short- and long-term follow-up in comparison to primary BDC resection[9-11]. Additionally, a few series have emphasized the negative impact of previous CE on results of secondary BDC resection[2]. Lastly, CE has been shown to be associated with an increased risk of cholangiocarcinoma[12,13]. Consequently, primary resection has been considered as the treatment of choice for BDC[9,14,15]. The purpose of the present study was to investigate the role of a previous CE on short and long-term outcomes after secondary cyst resection in a large European multicenter cohort of patients.

MATERIALS AND METHODS
Study population and patients’ data collection

A multicenter retrospective study was conducted under the auspices of the Association Française de Chirurgie. During a 37 years period (between 1974 and 2011), 33 centers (including 24 academic centers) from 6 different European countries have included a total of 505 patients operated from Todani type I, IVb, II, III, IVA BDC.

The patients’ medical records were included on a website database (http://www.chirurgie-viscerale.org) using an online computerized standardized questionnaire. Patients’ demographic data, previous history of surgical and/or endoscopic interventions for hepatobiliary and pancreatic (HBP) disease, clinical symptoms, biochemical and imaging studies, details of surgical procedures, pathological data, duration of follow-up and short- and long-term postoperative outcome were collected.

Additional data were obtained from e-mail exchanges or phone calls with the referral centers. Operative reports, pathology reports and imaging studies were systematically reviewed by the 3 senior authors (Jean-Yves Mabrut, Reza Kianmanesh and Jean François Gigot) in order to establish homogeneous disease classifications. Patients’ operative risk was evaluated by using the American Society of Anesthesiology physical status score (ASA)[16]. A pediatric patient was defined as under 15 years of age.

Complicated clinical presentation was defined by the presence of severe episodes of cholangitis or pancreatitis, portal hypertension, biliary peritonitis or coexistent synchronous carcinoma. Disease involvement of the main biliary confluence (MBC) was also classified according to the classification reported by two of the co-authors[17]. Postoperative morbidity and mortality were defined at 3 mo or during hospital stay. Postoperative morbidity was graded according to Dindo-Clavien’ classification[18]. Long-term outcome was evaluated according to the dedicated evaluation score reported by the Mayo Clinic[2]. Complete cyst excision was defined as without macroscopic dilatation of bile duct after resection.

BDC subtypes were defined based on imaging studies in accordance with the Todani classification[14]. Todani BDC subtypes included type I in 47.3% (n = 239), type II in 3.7 % (n = 19), type III in 2.5% (n = 13), type IVa in 14.4% (n = 73), type IVb in 1.2% (n = 6) and type V in 30.7% (n = 155). Only patient with isolated, extrahepative BDC disease (Type I and IVb) were included (n = 245). Two additional patients that did not undergoing resection were excluded and thus 243 were ultimately analyzed.

A pediatric patient was defined as being aged under 15 years of age. Patients’ operative risk was evaluated by using the ASA[16]. Complicated clinical presentation was defined by the presence of severe episodes of cholangitis or pancreatitis, portal hypertension, biliary peritonitis or coexistent synchronous carcinoma. Disease involvement of the MBC was also classified according to the classification reported by two of the co-authors[17]. Postoperative morbidity and mortality were defined at 3 mo or during hospital stay. Postoperative morbidity was graded according to Dindo-Clavien’ classification[18]. Long-term outcome was evaluated according to the dedicated evaluation score reported by the Mayo Clinic[2].

Statistical analysis

Comparisons between patient with and without CE were performed using the χ2 test (or the Fisher’s exact test when conditions for the χ2 test were not fulfilled) for categorical variables and using the Student t test (or the Mann-Whitney nonparametric rank sum test in case of non-normality) for continuous variables. Predictive factors of poor or fair result during long-term follow-up were analyzed by multivariate statistical analysis. Significant variables at the 0.15 level in univariate analysis were introduced in the multivariate logistic regression model. Kaplan-Meier analysis was used to predict the postoperative survival rate at 1 year and at 3 years. The log-rank test was used to compare subgroups of patients at 1 year and at 3 years. Statistical analysis was performed using SAS® version 9.2 (SAS Institute Inc, Cary, North Carolina, United States).

RESULTS

Patients were stratified based on a history of a previous CE. Demographic data, Todani BDC subtypes, types of imaging studies (Table 1), clinical presentations (Table 2), coexistent HBP diseases (Table 3), types of surgical procedures (Table 4), and short- and long-term postoperative outcomes (Table 5) were then compared between the two cohorts. Finally, predictive variables of poor/fair long-term outcome are reported in Table 6.

Table 1 Patients’ demographic data, todani bile duct cyst subtypes and imaging studies.
Patient with previous CEPatient without previous CETotalP value
Patients16227243-
Median age (yr) at the time of BDC resection47.8 (26-60)29.2 (0-81)30.8 (0-81)0.0074
Sex ratio F/M73.733.80.5359
Adults/children16/0148/79164/790.0041
ASA score1
1 or 215 (93.75%)217 (95.6%)232 (95.0%)0.5350
≥ 31 (6.3%)10 (4.4%)11 (4.5%)
Types of imaging studies
None (incidental detection)1 (6.3%)2 (0.9%)3 (1.2%)0.1855
Percutaneous ultrasound8 (50.0%)188 (82.8%)196 (80.7%)0.0042
Computed tomography7 (43.8%)119 (52.4%)126 (51.9%)0.5022
MR- cholangiography9 (56.3%)138 (60.8%)147 (60.5%)0.7194
ERCP7 (43.8%)40 (17.6%)47 (19.3%)0.0186
Endoscopic ultrasound8 (50.0%)36 (15.9%)44 (18.1%)0.0026
Percutaneous cholangiography017 (7.5%)17 (7.0%)0.6115
Intravenous cholangiography2 (12.5%)13 (5.7%)15 (6.2%)0.2583
Intraoperative cholangiography06 (2.6%)6 (2.5%)1.0000
Todani bile duct cyst types
Type I16221237
Type IVB0661.0000
MBC adequately analyzed12 (75%)196 (86%)208 (85.5%)
Cyst involvement of MBC5/12 (41.6%)47/196 (24.0%)52 (21.4%)0.3173
MBC-133942
MBC-228100.2420
Presence of PBM adequately explored10180190
Presence of anomalous PBM8 (80.0%)141 (78.3%)149 (78.4%)1.0000
Table 2 Patients’ clinical presentation.
Patients with previous CE n = 16Patients without previous CE n = 227Total n = 243P value
Median delay between symptoms and diagnosis (mo) (range)2 (0-486)2 (0-360)2 (0-486)0.8848
Type of symptoms and signs
Asymptomatic2 (12.5%)31 (13.7%)33 (13.6%)1.0000
Isolated pain2 (12.5%)104 (45.8%)106 (43.6%)0.0094
Cholangitis12 (75%)52 (22.9%)64 (26.3%)< 0.0001
Pancreatitis2 (12.5%)49 (21.6%)51 (21.0%)0.5344
Abdominal mass2 (12.5%)22 (9.7%)24 (9.9%)0.6631
Jaundice16 (37.5%)59 (26.0%)65 (27.2%)0.3843
Pruritus1 (6.2%)2 (0.9%)3 (1.2%)0.1855
Weight loss2 (12.5%)6 (2.6%)8 (3.2%)0.0903
Complicated presentation12 (75%)92 (40.5%)104 (42.8%)0.0071
Number of patients with > 2 symptoms9 (56.25%)92 (40.5%)102 (42.0%)0.2942
Table 3 Coexistent hepato-biliary and pancreatic diseases.
Patients with previous CE n = 16Patients without previous CE n = 227Total n = 243P value
Biliary disease9 (56.2%)52 (22.9%)61 (25.1%)0.0059
Common biliary atresia01 (0.4%)1 (0.4%)1.0000
Stones4 (25%)37 (16.3%)41 (16.9%)0.3216
Gallbladder016 (7.0%)16 (6.6%)-
Cyst3 (18.8%)9 (4.0%)12 (4.9%)-
Common bile duct1 (6.3%)22 (9.7%)23 (9.5%)-
Intra hepatic duct04 (1.8%)4 (1.6%)-
Synchronous cancer5 (31.3%)14 (6.2%)19 (7.8%)0.0043
Table 4 Preoperative treatment and types of surgery.
Patients with previous CE n = 16Patients without previous CE n = 227Total n = 243P value
Preoperative biliary drainage2 (12.5%)14 (6.2%)16 (6.6%)0.2842
Types of surgical procedures
Absence of resection1 (6.3%)5 (2.2%)6 (2.5%)0.3384
Elective surgery14 (87.5%)214 (94.3%)228 (93.8%)0.2583
Emergency surgery1 (6.2%)9 (4.0%)10 (4.1%)0.5007
Complete cyst excision13 (81.2%)199 (87.6%)212 (87.2%)0.6631
Incomplete cyst excision2 (12.5%)23 (10.1%)25 (10.3%)
Superior excision1 (6.3%)13 (5.7%)14 (5.8%)
Inferior excision1 (6.3%)9 (4.0%)10 (4.1%)-
Unknown01 (0.4%)1 (0.4%)
Associated procedures
Hepatectomy2 (12.5%)4 (1.8%)6 (2.5%)0.0523
Pancreaticoduodenectomy4 (25.0%)4 (1.8%)8 (3.3%)0.0008
Stone extraction2 (12.5%)10 (4.4%)12 (4.9%)0.2072
Synchronous cancer excision5 (31.3%)13 (5.7%)118 (7.8%)0.0043
Biliary reconstruction
Hepatico-jejunostomy13 (81.2%)208 (91.6%)221 (90.9%)0.1658
Hepatico-duodenostomy2 (12.5%)7 (3.1%)9 (3.7%)0.1116
Choledoco-duodenostomy01 (0.4%)1 (0.4%)1.0000
MBC anastomosis8/14 (57.1%)96/180 (53.3%)104/194 (53.6%)0.7831
Table 5 Early postoperative and long term outcome of patients.
Patients with previous CE n = 16Patients without previous CE n = 227Total n = 243P value
Median postoperative hospital stay (d) (range)16 (9-110)10 (2-150)10 (2-150)0.0014
Mortality rate0 (0.0%)1 (0.4%)1 (0.4%)1.0000
Overall complications12 (75.0%)75 (33%)87 (35.8%)0.0018
Grade I-II5 (31.3%)47 (20.9%)52 (21.4%)0.3454
Grade III-IV7 (43.8%)28 (12.3%)35 (15.4%)0.0031
Surgical complications7 (43.8%)45 (19.8%)52 (21.4%)0.0509
Biliary0 (0.0%)20 (8.8%)20 (8.2%)0.3750
Mixed pancreatic and biliary fistula1 (6.3%)5 (2.2%)6 (2.5%)0.3384
Pancreatic1 (6.3%)17 (7.5%)18 (7.4%)1.0000
Bleeding5 (31.3%)3 (1.3%)8 (3.3%)< 0.0001
Reoperation rate6 (37.5%)20 (8.8%)26 (10.7%)0.0032
Long-term outcome of patients
Patients with previous CE n = 13Patients without previous CE n = 185n = 198
Median follow-up (mo) (range)59 (12-175)36 (4-372 )37.5 (4-372)0.2482
Mayo clinic score
Excellent5 (38.5%)138 (74.6%)143 (72.2%)
Good2 (15.4%)18 (9.7%)20 (10.1%)0.0099
Fair05 (2.7%)5 (2.5%)
Poor6 (46.2%)24 (13.0%)30 (15.1%)
Mayo clinic score
Excellent + good7 (53.8%)156 (84.3%)163 (82.3%)0.0136
Fair + poor6 (46.2%)29 (15.7%)35 (17.7%)
Table 6 Predictive factors of poor and fair long-term outcome according to Mayo clinic score in 198 patients with a follow-up > 3 mo, including patients suffering from synchronous cancer.
CovariateUnivariate
Multivariate
OR95%CIP valueOR95%CIP value
Adult patient vs child3.5871.322-9.7350.0084---
Previous cyst-enterostomy; Yes vs No4.6111.445-14.7120.01363.1650.829-12.0770.0918
Synchronous cancer; Yes vs No18.4624.687-72.71< 0.000116.6123.999-69.0130.0001
Post-operative complications; Yes vs No2.3971.143-5.0280.0186---
Postoperative biliary complications; Yes vs No4.3561.669-11.3670.00384.5971.635-12.9250.0038
Patients’ demographic data, todani BDC subtypes and types of imaging studies

During a 37-year period (1974-2011), 243 patients underwent resections for Todani types I and IVb congenital BDC at 33 centers (including 24 academic centers). The patients’ gender ratio was largely female (193/50, i.e., 3.86%). Median age was 30.8 years old (range: 0.1-81 years) and 79 patients were classified at pediatric. Patients’ characteristics are detailed in Table 1. Sixteen patients had undergone previous CE (16/243, i.e., 6.58%), they were all adults (100% vs 65.2%; P = 0.0041) and significantly older (47.8-year-old vs 29.2-year-old; P = 0.0074) than those without a history of CE. Imaging studies used for the diagnosis of BDC were different between the 2 groups: Patients without previous history of CE were offered more non-invasive studies, whereas those patients with previous CE had been submitted to significantly more endoscopic techniques. There was no difference concerning the BDC sub-types, the MBC involvement and the presence of an anomalous pancreato-biliary malunion (PBM) (Table 1).

Clinical presentation

The median delay between the disease’s first symptoms and the diagnosis of BDC was 2 mo (0-486) and was similar between the 2 groups of patients. Abdominal pain was the most common presenting symptom (43.6%) for the whole population and significantly more frequent in patients without previous CE (12.5% vs 45.8%; P = 0.009). The group of patients with previous CE was observed to have a significantly increased prevalence of cholangitis (75.0% vs 22.9%; P < 0.0001) and complicated presentation (75.0% vs 40.5%; P = 0.007) (Table 2).

Coexistent HBP diseases

Coexistent biliary disease (liver disease, pancreatic disease, and biliary disease) occurred in 25.1% of the present cohort and was significantly more frequent in patients with previous CE (56.2% vs 22.9%; P = 0.006). The occurrence of associated calculus disease (16.9%) was similar between the two groups. Synchronous biliary cancer occurred in 7.8% of the total cohort and was significantly more frequent in patients with previous CE (31.3% vs 6.2%; P = 0.004) (Table 3).

Preoperative treatment and type of surgery

Preoperative biliary drainage was performed in 6.6% of the whole cohort. All patients underwent surgical exploration. However, 5 adult patients without CE did not undergo BDC resection, one for no specified reason, the others respectively for locally advanced gallbladder cancer, peritoneal carcinomatosis, severe inflammation of the hepatic pedicle, performance of simple cholecystectomy. Only one patient with previous CE had severe hepatic pedicle inflammation prohibiting cyst resection. Associated bile duct stone extraction rates were similar between the two subgroups. Complete cyst excision was accomplished in 93.8% of all patients and there was no significant difference between the two groups of patients. Associated hepatectomy was more frequently performed in patients with previous CE but the difference was not significant (12.5% vs 1.8%; P = 0.0523). Associated pancreaticoduodenectomy was significantly more frequent in patients with previous CE (25% vs 1.8%; P = 0.008) (Table 4).

Postoperative mortality, morbidity and early postoperative outcome (within 3 mo)

Postoperative death due to cardiac arrhythmia, occurred in 1 patient (0.4%). Overall morbidity and severe complications rates were 36.2% and 14%, respectively. Patients with previous CE had significantly higher morbidity rates (75.0% vs 33.5%; P < 0.0008), more severe complications (Grade III-IV) (43.8% vs 11.9%; P = 0.003), more hemorrhagic complications (31.3% vs 1.3%; P < 0.0001), a greater reoperation rate (37.5% vs 8.8%; P = 0.003) and a longer median length of stay (16 vs 10 d; P < 0.001) than those without previous CE (Table 5).

Postoperative long-term outcome

A total of 44 patients were lost for follow-up at 3 mo, only 3 of whom belonged to the subgroup of patients with previous CE. The median follow-up in the 198 remaining patients was 37.5 mo (range: 4 to 732 mo) for the whole cohort, without any difference between both subgroups. According to the dedicated Mayo Clinic Risk score evaluating long-term results, there were significantly more patients with fair and poor results in the subgroup of patients with previous CE (P = 0.001). The overall 3-year survival rate was significantly lower in patients with prior CE (82.5% vs 95.9%; P = 0.01) (Figure 1) (Table 5).

Figure 1
Figure 1 Comparison of overall survival between patients operated from bile duct cysts with and without previous history of cyst-enterostomy.
Univariate and multivariate analysis

Predictive variables of poor and fair long-term results (according to the Mayo Clinic clinical score) were evaluated in the 198 patients surviving surgery and with a follow-up over 3 mo. Univariate statistical analysis indicated that predictive variables of poor or fair long-term results were to be an adult patient, with prior CE, postoperative complications, postoperative biliary complications and coexistent synchronous cancer. By multivariate analysis, predictive variables of poor or fair long-term results were previous CE, synchronous cancer and postoperative biliary complications (Table 6).

DISCUSSION

The present retrospective series shows that patients submitted to secondary resection of congenital BDC following a previous cyst-enterostomy suffered more complications before, during and after surgery with poorer results during long-term follow-up. Strengths of the present series include the relatively large cohort of patients issued from a multicentric European series, and the central revision of radiological, operative and pathological data, thereby ensuring a homogeneous classification of patients and their symptoms and signs both prior and after surgery, with the use of a dedicated clinical score for long-term results. Furthermore, the analysis was performed in a homogeneous group of BDC with only extrahepatic biliary involvement, namely patients suffering from Todani types I and IVb BDC. Indeed, patients with Todani type IVA were excluded from the present series so that poor results could not be due to residual non-resected intrahepatic biliary disease.

According to the results of the present study, primary complete excision of BDC, with the construction of a wide bilio-digestive anastomosis to a healthy proximal bile duct should be the “gold standard” surgical management of patients suffering from BDC[2,14,19]. Cyst-enterostomy must definitively be abandoned as a treatment option. Limitations of the study include its retrospective design, its long period (37 years) of patients inclusion and the number of patients without available long-term follow-up. The comparison between patients with previous cyst-enterostomy and the control group should also be considered with caution due to the small number of patients in the CE group.

However, despite cyst-enterostomy being no longer the primary approach for the surgical management of BDC, its prevalence was 17.2% in 186 patients operated on after 1980[2,7,20-22] and previous cyst-enterostomy was still observed in 7.3% of 354 patients operated on after 1990[23-26]. Practically, this means that previous CE still remains a challenge during the management of BDC.

Indeed, the consequences of having undergone a cyst-enterostomy, regardless of the technique used, easily explain the more complicated clinical presentation of previously operated patients encountered in the present series: Possible mechanisms include reflux of digestive juice through the entire biliary tract, activation of pancreatic juice by enterokinases linked to pancreatico-biliary malunion[27] or even anastomotic stricture of the CE on diseased cystic biliary tissue[19,28,29]. Any of these can lead to severe biliary inflammation[15], cholangitis, hepatolithiasis[10,19,30,31] and increase the risk of carcinogenesis[12,13,19,27]. The latter is estimated to be over 50% by Todani et al[27]. Indeed, malignant degeneration of BDC occurs more than 15 years earlier in patients with previous CE than in patients with primary carcinomas, with a median delay of 4 years in a series by Flanigan et al[13] to 10 years (range: 1-53 years of delay) in yet another by Todani et al[27] and, overall, is associated with a very poor prognosis. Finally, the reoperation rate after previous CE is high, ranging from 15.7% to 87.5%[1,9,30,32].

The present series also shows that more complex surgical procedures had to be used for patients with a previous CE, mainly due to an increased need for a pancreaticoduodenectomy. Such an extensive procedure was linked, for half of these patients, with the presence of coexistent carcinoma, thereby, requiring tumor resection with a wide tumor-free margin. The other pancreaticoduodenectomies were mainly performed because of severe inflammation within the hepatic pedicle, probably as a result of repeated episodes of cholangitis. This feature observed during secondary BDC resection in patients with previous CE has not been reported until now.

According to several surgical series which compared primary CE with primary BDC resection with Roux-en-Y hepaticojejunostomy have reported an increased mortality rate (range: 8.3%-10% vs 0%-7%), morbidity rate (range: 17%-93% vs 0%-17%) and reoperation rate (range: 29.7%-87.5% vs 0%) in patients with primary CE[9,10,30]. At the time of writing, there are only 3 studies that compared the morbidity and mortality rates between primary BDC resection and secondary BDC resection with previous CE, and these concerned series with only small numbers of patients[2,15,19]. For patients with previous CE, Chijiiwa et al[19] and Gigot et al[2] observed significantly more early postoperative complications, whilst Kaneko et al[15] reported significantly increased operative blood losses, operative time, early postoperative complications and wound infections. The present series demonstrates similar findings of an increased rate of overall and severe postoperative complications as well as hemorrhagic complications and reoperation rates for patients operated following previous CE.

The key-messages of this first large European multicenter study are that BDC patients who have undergone previous CE have more complications including carcinoma, that long-term results and survival rate are worse and that the reoperation rate is greater. It should be emphasized that these results cannot be attributed to intrahepatic disease alone as only Todani type I and IVb lesions were studied in this analysis. Late complications were also increased in the series reported by Kaneko et al[15], especially regarding late development of hepatolithiasis and pancreatic stones, though this was not reported in the series by Chijiiwa et al[19]. Finally, multivariate statistical analysis confirmed in the present series that previous CE was representing an independent predictive factor of fair or poor prognosis after secondary BDC resection. Weaknesses of the present study include its retrospective nature, the number of patients excluded from long-term follow-up after 3 mo (18.1% of the whole series), the limited median follow-up duration of 37.5 mo and the small numbers of patients with previous CE.

In conclusion, this European retrospective series showed that previous CE was associated with a more complicated presentation, more coexistent HPB diseases including synchronous cancer, more complex surgery and worse early and long-term postoperative outcomes. These features confirmed the abandonment of cyst-enterostomy for the surgical management of congenital bile duct cysts.

ACKNOWLEDGMENTS
The AFC Working Group

Jean De Ville de Goyet1, Catherine Hubert1, Jan Lerut1, Jean-Bernard Otte1, Raymond Reding1, Olivier Farges2, Alain Sauvanet2, Gilles Mentha3, Oulhaci Wassila3, Barbara Wildhaber3, Felice Giulante4, Francesco Ardito4, Maria De rose Agostino4, Thomas Gelas5, Pierre-Yves Mure5, Jacques Baulieux6, Christian Gouillat6, Ducerf Christian6, Sabine Irtan7, Sabine Sarnacki7, Alexis Laurent8, Philippe Compagnon8, Chady Salloum8, Roger Lebeau9, Olivier Risse9, Stéphanie Truant10, Emmanuel Boleslawski10, François Corfiotti10, Alexandre Doussot11, Pablo Ortega-Deballon11, Pierre Balladur12, Mustapha Adham13, Christian Partensky13, Taore Alhassane13, Catelin Tiuca Dane14, Yves-Patrice Le Treut15, Mathieu Rinaudo15, Jean Hardwigsen15, Hélène Martelli16, Frédéric Gauthier16, Sophie Branchereau16, Simon Msika17, Daniel Sommacale18, Jean-Pierre Palot 18, Ahmet Ayav19, Charles-Alexandre Laurain19, Massimo Falconi20, Denis Castaing21, Oriana Ciacio21, René Adam21, Eric Vibert 21, Roberto Troisi22, Aude Vanlander22, Stéphane Geiss23, Gilles De Taffin23, Denis Collet24, Antonio Sa Cunha24, Laurent Duguet25, Bouzid Chafik26, Kamal Bentabak26, Abdelaziz Graba26, Nicolas Meurisse27, Jacques Pirenne27, Lorenzo Capussotti28, Serena Langelle28, Nermin Halkic29, Nicolas Demartines29, Alessandra Cristaudi29, Gaëtan Molle30, Baudouin Mansvelt30, Massimo Saviano31, Gelmini Roberta31, Ousema Baraket32, Samy Bouchoucha32, Bernard Sastre33.

From

1Cliniques Universitaires Saint- Luc, Brussels, Belgium , 2Beaujon Hospital, Clichy, France, 3Geneva University Hospital, Geneva, Switzerland, 4Gemelli University Hospital, Roma, Italy, 5Mother and Children Hospital, Lyon, France, 6La Croix-Rousse Hospital, Lyon, France, 7Necker Hospital, Paris, France, 8Henri Mondor Hospital, Creteil, France, 9Michallon Hospital, Grenoble, France, 10Claude Huriez Hospital, Lille, France, 11Dijon University Hospital, Dijon, France, 12Saint Antoine Hospital, Paris, France, 13Edouard-Herriot Hospital, Lyon, France, 14Rennes University Hospital, Rennes, France, 15Conception Hospital, Marseille, France, 16Bicetre Hospital, Paris, France, 17Louis Mourier Hospital, Colombes, France, 18Robert Debré Hospital, Reims, France, 19Nancy University Hospital, Nancy, France, 20Negrar University Hospital, Verona, Italy, 21Paul-Brousse Hospital, Paris, France, 22Amiens University Hospital, Amiens, France, 22Ghent University Hospital, Ghent, Belgium, 23Le Parc Hospital, Colmar, France, 24Bordeaux University Hospital, Bordeaux, France, 25Sainte Camille Hospital, Bry-sur-Marne, France, 26Pierre et Marie Curie Hospital, Alger, Algeria, 27UZ Leuven University Hospital, Leuven, Belgium, 28Mauriziano University Hospital, Torino, Italy, 29Vaudois University Hospital, Lausanne, Switzerland, 30Jolimont Hospital, La Louvière, Belgium, 31Modena University Hospital, Modena, Italy, 32Habib Boughefta Hospital, Bizertz, Tunisia, 33La Timone Hospital, Marseille, France.

The authors thank the staff and patients of all the participating hospitals for helping with the gathering of all the necessary information for this retrospective study. They are also grateful to Professor Claire Craddock-de Burbure for her meticulous reading of the manuscript.

COMMENTS
Background

Congenital bile duct cysts (BDC) are rare in the United States and in Europe. Cyst-enterostomy has been reported to be associated with increased morbidity (especially biliary complications) and higher reoperation rates during short- and long-term follow-up in comparison to primary BDC resection. Consequently, primary resection has been considered as the treatment of choice for BDC. The purpose of the present study was to investigate the role of a previous cyst-enterostomy (CE) on short and long-term outcomes after secondary cyst resection in a large European multicenter cohort of patients.

Research frontiers

Limitation of the study includes its retrospective design, its long period (37 years), included patients and the number of patients without available long-term follow-up. The comparison between patients with previous cyst-enterosotmy and the comtrol group should also be considered with caution due to the small number of patients in the CE group. However, despite cyst-enterostomy being no longer the primary approach for the surgical management of BDC, its prevalence was 17.2% in 186 patients operated on after 1980 and previous cyst-enterostomy was still observed in 7.3% of 354 patients operated on after 1990. Practically, this means that previous CE still remains a challenge during the management of BDC.

Innovations and breakthroughs

This European retrospective series showed that previous CE was associated with a more complicated presentation, more coexistent HPB diseases including synchronous cancer, more complex surgery and worse early and long-term postoperative outcomes. These features confirmed the abandonment of cyst-enterostomy for the surgical management of congenital bile duct cysts.

Applications

These features confirmed the abandonment of cyst-enterostomy for the surgical management of congenital bile duct cysts.

Peer-review

The results of this European multicenter study are very interesting and the manuscript is well-written.

Footnotes

P- Reviewer: Guan YS, Kleeff J, Klinge U S- Editor: Qiu S L- Editor: A E- Editor: Wu HL

References
1.  Yamaguchi M. Congenital choledochal cyst. Analysis of 1,433 patients in the Japanese literature. Am J Surg. 1980;140:653-657.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 321]  [Cited by in F6Publishing: 261]  [Article Influence: 5.9]  [Reference Citation Analysis (0)]
2.  Gigot JF, Nagorney DM, Farnell MB, Moir C, Ilstrup D. Bile duct cysts: A changing spectrum of presentation. J Hep Bil Pancr Surg. 1996;3:405-411.  [PubMed]  [DOI]  [Cited in This Article: ]
3.  Söreide K, Körner H, Havnen J, Söreide JA. Bile duct cysts in adults. Br J Surg. 2004;91:1538-1548.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 129]  [Cited by in F6Publishing: 113]  [Article Influence: 5.7]  [Reference Citation Analysis (0)]
4.  Kimura K, Tsugawa C, Ogawa K, Matsumoto Y, Yamamoto T, Kubo M, Asada S, Nishiyama S, Ito H. Choledochal cyst. Etiological considerations and surgical management in 22 cases. Arch Surg. 1978;113:159-163.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 30]  [Cited by in F6Publishing: 31]  [Article Influence: 0.7]  [Reference Citation Analysis (0)]
5.  Hays DM, Goodman GN, Snyder WH, Woolley MM. Congenital cystic dilatation of the common bile duct. Arch Surg. 1969;98:457-461.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 35]  [Cited by in F6Publishing: 35]  [Article Influence: 0.6]  [Reference Citation Analysis (0)]
6.  Jones PG, Smith ED, Clarke AM, Kent M. Choledochal cysts: experience with radical excision. J Pediatr Surg. 1971;6:112-120.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 23]  [Cited by in F6Publishing: 24]  [Article Influence: 0.5]  [Reference Citation Analysis (0)]
7.  Lenriot JP, Gigot JF, Ségol P, Fagniez PL, Fingerhut A, Adloff M. Bile duct cysts in adults: a multi-institutional retrospective study. French Associations for Surgical Research. Ann Surg. 1998;228:159-166.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 78]  [Cited by in F6Publishing: 82]  [Article Influence: 3.2]  [Reference Citation Analysis (0)]
8.  Alonso-Lej F, Rever WB, Pessagno DJ. Congenital choledochal cyst, with a report of 2, and an analysis of 94, cases. Int Abstr Surg. 1959;108:1-30.  [PubMed]  [DOI]  [Cited in This Article: ]
9.  Flanigan PD. Biliary cysts. Ann Surg. 1975;182:635-643.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 188]  [Cited by in F6Publishing: 194]  [Article Influence: 4.0]  [Reference Citation Analysis (0)]
10.  Saing H, Tam PK, Lee JM. Surgical management of choledochal cysts: a review of 60 cases. J Pediatr Surg. 1985;20:443-448.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 16]  [Cited by in F6Publishing: 18]  [Article Influence: 0.5]  [Reference Citation Analysis (0)]
11.  Plata-Muñoz JJ, Mercado MA, Chan C, González QH, Orozco H. Complete resection of choledochal cyst with Roux-en-Y derivation vs. cyst-enterostomy as standard treatment of cystic disease of the biliary tract in the adult patient. Hepatogastroenterology. 2005;52:13-16.  [PubMed]  [DOI]  [Cited in This Article: ]
12.  Todani T, Tabuchi K, Watanabe Y, Kobayashi T. Carcinoma arising in the wall of congenital bile duct cysts. Cancer. 1979;44:1134-1141.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in F6Publishing: 2]  [Reference Citation Analysis (0)]
13.  Flanigan DP. Biliary carcinoma associated with biliary cysts. Cancer. 1977;40:880-883.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in F6Publishing: 2]  [Reference Citation Analysis (0)]
14.  Todani T, Watanabe Y, Narusue M, Tabuchi K, Okajima K. Congenital bile duct cysts: Classification, operative procedures, and review of thirty-seven cases including cancer arising from choledochal cyst. Am J Surg. 1977;134:263-269.  [PubMed]  [DOI]  [Cited in This Article: ]
15.  Kaneko K, Ando H, Watanabe Y, Seo T, Harada T, Ito F, Niimi N, Nagaya M, Umeda T, Sugito T. Secondary excision of choledochal cysts after previous cyst-enterostomies. Hepatogastroenterology. 1999;46:2772-2775.  [PubMed]  [DOI]  [Cited in This Article: ]
16.  Owens WD, Felts JA, Spitznagel EL. ASA physical status classifications: a study of consistency of ratings. Anesthesiology. 1978;49:239-243.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 1437]  [Cited by in F6Publishing: 1429]  [Article Influence: 31.1]  [Reference Citation Analysis (0)]
17.  Mabrut JY, Partensky C, Gouillat C, Baulieux J, Ducerf C, Kestens PJ, Boillot O, de la Roche E, Gigot JF. Cystic involvement of the roof of the main biliary convergence in adult patients with congenital bile duct cysts: a difficult surgical challenge. Surgery. 2007;141:187-195.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 8]  [Cited by in F6Publishing: 8]  [Article Influence: 0.4]  [Reference Citation Analysis (0)]
18.  Dindo D, Demartines N, Clavien PA. Classification of surgical complications: a new proposal with evaluation in a cohort of 6336 patients and results of a survey. Ann Surg. 2004;240:205-213.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 18532]  [Cited by in F6Publishing: 21934]  [Article Influence: 1096.7]  [Reference Citation Analysis (0)]
19.  Chijiiwa K. Hazard and outcome of retreated choledochal cyst patients. Int Surg. 1993;78:204-207.  [PubMed]  [DOI]  [Cited in This Article: ]
20.  Cheng SP, Yang TL, Jeng KS, Liu CL, Lee JJ, Liu TP. Choledochal cyst in adults: aetiological considerations to intrahepatic involvement. ANZ J Surg. 2004;74:964-967.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 15]  [Cited by in F6Publishing: 19]  [Article Influence: 1.0]  [Reference Citation Analysis (0)]
21.  Durgun AV, Gorgun E, Kapan M, Ozcelik MF, Eryilmaz R. Choledochal cysts in adults and the importance of differential diagnosis. J Hepatobiliary Pancreat Surg. 2002;9:738-741.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 6]  [Cited by in F6Publishing: 6]  [Article Influence: 0.3]  [Reference Citation Analysis (0)]
22.  Lal R, Agarwal S, Shivhare R, Kumar A, Sikora SS, Saxena R, Kapoor VK. Type IV-A choledochal cysts: a challenge. J Hepatobiliary Pancreat Surg. 2005;12:129-134.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 28]  [Cited by in F6Publishing: 28]  [Article Influence: 1.5]  [Reference Citation Analysis (0)]
23.  Cho MJ, Hwang S, Lee YJ, Kim KH, Ahn CS, Moon DB, Lee SK, Kim MH, Lee SS, Park DH. Surgical experience of 204 cases of adult choledochal cyst disease over 14 years. World J Surg. 2011;35:1094-1102.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 60]  [Cited by in F6Publishing: 58]  [Article Influence: 4.5]  [Reference Citation Analysis (0)]
24.  Shah OJ, Shera AH, Zargar SA, Shah P, Robbani I, Dhar S, Khan AB. Choledochal cysts in children and adults with contrasting profiles: 11-year experience at a tertiary care center in Kashmir. World J Surg. 2009;33:2403-2411.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 50]  [Cited by in F6Publishing: 53]  [Article Influence: 3.8]  [Reference Citation Analysis (0)]
25.  Visser BC, Suh I, Way LW, Kang SM. Congenital choledochal cysts in adults. Arch Surg. 2004;139:855-860; discussion 860-862.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 106]  [Cited by in F6Publishing: 119]  [Article Influence: 6.0]  [Reference Citation Analysis (0)]
26.  Woon CY, Tan YM, Oei CL, Chung AY, Chow PK, Ooi LL. Adult choledochal cysts: an audit of surgical management. ANZ J Surg. 2006;76:981-986.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 20]  [Cited by in F6Publishing: 20]  [Article Influence: 1.2]  [Reference Citation Analysis (0)]
27.  Todani T, Watanabe Y, Toki A, Urushihara N. Carcinoma related to choledochal cysts with internal drainage operations. Surg Gynecol Obstet. 1987;164:61-64.  [PubMed]  [DOI]  [Cited in This Article: ]
28.  Todani T, Watanabe Y, Toki A, Urushihara N, Sato Y. Reoperation for congenital choledochal cyst. Ann Surg. 1988;207:142-147.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 93]  [Cited by in F6Publishing: 97]  [Article Influence: 2.7]  [Reference Citation Analysis (0)]
29.  Joseph VT. Surgical techniques and long-term results in the treatment of choledochal cyst. J Pediatr Surg. 1990;25:782-787.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 69]  [Cited by in F6Publishing: 71]  [Article Influence: 2.1]  [Reference Citation Analysis (0)]
30.  Deziel DJ, Rossi RL, Munson JL, Braasch JW, Silverman ML. Management of bile duct cysts in adults. Arch Surg. 1986;121:410-415.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 56]  [Cited by in F6Publishing: 59]  [Article Influence: 1.6]  [Reference Citation Analysis (0)]
31.  Takiff H, Stone M, Fonkalsrud EW. Choledochal cysts: results of primary surgery and need for reoperation in young patients. Am J Surg. 1985;150:141-146.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 17]  [Cited by in F6Publishing: 20]  [Article Influence: 0.5]  [Reference Citation Analysis (0)]
32.  Powell CS, Sawyers JL, Reynolds VH. Management of adult choledochal cysts. Ann Surg. 1981;193:666-676.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 55]  [Cited by in F6Publishing: 61]  [Article Influence: 1.4]  [Reference Citation Analysis (0)]