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      Le syndrome de Mirizzi: une cause rare de l’obstruction des voies biliaires: à propos d’un cas et revue de littérature Translated title: Mirizzi’s syndrome: a rare cause of biliary tract obstruction: about a case and review of the literature

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          Abstract

          Le syndrome de Mirizzi est une complication rare de la lithiase vésiculaire chronique, avec une incidence de 0,7% à 1,4% chez les malades cholécystéctomisés. Il est caractérisé par un ictère cholestatique en rapport avec une compression de la voie biliaire principale par un calcul enclavé dans le collet vésiculaire ou le canal cystique. La maladie peut évoluer vers l’érosion de la paroi du canal hépatique commun et par conséquent, provoquer la formation d’une fistule cholécysto-bilaire. Nous présentons ici un syndrome de Mirizzi type I en soulignant l’importance du diagnostic préopératoire, celui-ci étant rendu plus aisé par la cholangiographie rétrograde endoscopique ou par la cholangio-IRM, qui permet d’éviter des lésions iatrogènes de la voie biliaire principale. Le présent article passe en revue la littérature disponible sur les divers aspects de ce syndrome, y compris sa pathogenèse, son diagnostic et sa prise en charge.

          Translated abstract

          Mirizzi’s syndrome is a rare complication of chronic vesicular lithiasis with prevalence ranging from 0.7% to 1.4% among patients who have undergone cholecystectomy. It is characterized by cholestatic icterus associated with compression of the common bile duct due to lodged calculus in the vesicular neck or in the cystic duct. The disease can evolve toward the erosion through the common hepatic duct wall and, therefore, it can cause the formation of a gallbladder-biliary fistula. We here report a case of Mirizzi’s syndrome type I in order to highlight the role of preoperative diagnosis which is made easier by endoscopic retrograde cholangiography or by cholangio-MRI, allowing to avoid iatrogenic bile duct injuries. We conducted a review of the available literature on various aspects of this syndrome, including its pathogenesis, diagnosis and management.

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          Mirizzi syndrome and cholecystobiliary fistula: a unifying classification.

          A new classification of patients with Mirizzi syndrome and cholecystobiliary fistula is presented. Type I lesions are those with external compression of the common bile duct. In type II lesions a cholecystobiliary fistula is present with erosion of less than one-third of the circumference of the bile duct. In type III lesions the fistula involves up to two-thirds of the duct circumference and in type IV lesions there is complete destruction of the bile duct. A total of 219 patients were identified with these lesions from 17,395 patients with benign biliary tract diseases undergoing surgery. The incidence of type I lesions was 11 per cent, type II 41 per cent, type III 44 per cent and type IV 4 per cent. The majority had obstructive jaundice. In type I lesions, cholecystectomy plus choledochostomy is effective. In type II lesions, suture of the fistula with absorbable material or choledochoplasty with the remnant of gallbladder can be performed. In type III lesions suture is not indicated and choledochoplasty is recommended. In type IV lesions, bilioenteric anastomosis is preferred. Operative mortality rate increases according to the severity of the lesion, as does postoperative morbidity. During cholecystectomy, partial resection is recommended in order to extract the stones, visualize the common bile duct and define the type and location of the fistula. T tubes should be placed distal to the fistula.
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            Mirizzi's syndrome--results from a large western experience.

            This paper reports a series of patients with Mirizzi's syndrome (MS) who were managed at our institution over an 11-year (1994-2005) period.
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              Benign obstruction of the common hepatic duct (Mirizzi syndrome): diagnosis and operative management.

              Mirizzi syndrome is a rare complication of prolonged cholelithiasis, characterized by narrowing of the common hepatic duct due to mechanical compression and/or inflammation due to biliary calculus impacted in the infundibula of the gallbladder or in the cystic duct. To describe a series of eight consecutive patients with Mirizzi syndrome, at a single institution, submitted to surgical treatment and to comment on their aspects with emphasis on the diagnosis and treatment. Four women and four men, with a mean age of 61.6 years (42 to 82 years), presenting Mirizzi syndrome were operated between 1997 and 2003. The following items were evaluated: clinical presentation, laboratory results, preoperative evaluation, operative findings, presence of choledocholithiasis, type of Mirizzi syndrome according to the classification by Csendes, choice of operative procedures, and complications. The most frequent symptoms were abdominal pain (87.5%) and jaundice (87.5%). All the patients presented altered hepatic function tests. The diagnosis of Mirizzi syndrome was intra-operative in seven (87.5%) patients, and preoperative in one (12.5%). Cholecystocholedochal fistula associated with choledocholithiasis was observed in three (37.5%) cases. Mirizzi syndrome was classified as Csendes type I in five (62.5%) patients, type II in one (12.5%), type III in one (12,5%) and type IV in another (12.5%). Cholecystectomy, as an isolated surgical procedure, was performed in four (50.0%) patients. One (12.5%) patient was submitted to partial cholecystectomy and closure of the fistulous orifice with the central part of the infundibula. Two (25.0%) patients were submitted to cholecystectomy and side-to-side choledochoduodenostomy and another (12.5%) to side-to-side choledochoduodenostomy remaining the gallbladder in situ. Seven (87.5%) patients had an uneventful recovery and were discharged in good conditions. One (12.5%) patient presented a postoperative sepsis due to a sub-hepatic abscess, and was reoperated. There was no operative mortality. The preoperative diagnosis of Mirizzi syndrome is difficult and an awarded suspicion is necessary to avoid lesions of the biliary tree. The problem may only become evident during the operation due to firm adherences around Calot's triangle. The success of the treatment is related to a precocious recognition of the condition, even at the time of surgery, and adapting the management considering to the individual characteristics of each case.
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                Author and article information

                Journal
                Pan Afr Med J
                Pan Afr Med J
                PAMJ
                The Pan African Medical Journal
                The African Field Epidemiology Network
                1937-8688
                18 May 2017
                2017
                : 27
                : 45
                Affiliations
                [0001]¹Service d’imagerie médicale, Hôpital Militaire Mohamed V, Faculté de médecine et de pharmacie, Rabat, Maroc
                [0002]²Service des urgences médico-chirurgicales, Hôpital Militaire Mohamed V, Faculté de médecine et de pharmacie, Rabat, Maroc
                Author notes
                [& ]Corresponding author: Naoufal Chouaib, Service des Urgences Médico-chirurgicales, Hôpital Militaire Mohamed V, Faculté de Médecine et de Pharmacie, Rabat, Maroc
                Article
                PAMJ-27-45
                10.11604/pamj.2017.27.45.12469
                5554672
                f1c9d7c2-04b3-4a60-895d-8018def413bd
                © Habib Bellamlih et al.

                The Pan African Medical Journal - ISSN 1937-8688. This is an Open Access article distributed under the terms of the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 09 April 2017
                : 28 April 2017
                Categories
                Case Report

                Medicine
                syndrome de mirizzi,ictère,cholangiographie rétrograde endoscopique,fistule,cholécysto-biliaire,mirizzi’s syndrome,jaundice,endoscopic retrograde cholangiography,gallbladder,biliary fistula

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