[Monolobar Caroli's disease. Apropos of 12 cases]

Détails

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Etat: Public
Version: Final published version
Licence: Non spécifiée
ID Serval
serval:BIB_58538248A00A
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
[Monolobar Caroli's disease. Apropos of 12 cases]
Périodique
Chirurgie
Auteur⸱e⸱s
Gillet M., Favre S., Fontolliet C., Halkic N., Mantion G., Heyd B.
ISSN
0003-3944
Statut éditorial
Publié
Date de publication
1999
Peer-reviewed
Oui
Volume
124
Numéro
1
Pages
13-18
Langue
français
Notes
DA - 19990427 LA - fre PT - Comparative Study PT - English Abstract PT - Journal Article Titre original : Maladie de Caroli monolobaire. A propos de 12 cas SB - IM
Résumé
BACKGROUND: Caroli's disease is the dilatation of the segmental intrahepatic bile ducts. It usually affects the entire liver but can occasionally involve only one lobe, commonly the left. This study included 12 cases of unilobular disease, nine localised in the left lobe and three in the right lobe, which were all treated by liver resection. PATIENTS AND METHODS: These 12 patients underwent surgery between 1974 and 1997. There were six men and six women (mean age: 51 years). The initial presentation and diagnosis were reported. The mean interval between the first symptoms and diagnosis was 12.5 years. Eight of the 12 patients had undergone 22 surgical or endoscopic procedures prior to liver resection. In the present series a preoperative ultrasonogram or CT scan established the diagnosis in all cases. Six patients did not have stones in the gallbladder. RESULTS: Surgical treatment consisted in seven left lobectomies, two left hepatectomies and three right hepatectomies (Couinaud's classification). A intrahilar cholangiojejunostomy was performed in five cases. Pathological examination showed cystic dilatation of the intrahepatic segmental and subsegmental bile ducts, measuring from a few millimetres to 4 cm, which contained calculi. Two cases were associated with congenital hepatic fibrosis. An intrahepatic focus of ectopic pancreatic tissue was seen in one case. There were no cases with cholangiocarcinoma. One patient developed a biliary fistula which required reoperation. All patients had an uneventful long term postoperative course except for one patient who died of colon carcinoma 3 years postoperatively. CONCLUSION: When associated with other malformations, most notably congenital hepatic fibrosis, this commonly diffuse disease is called Caroli's syndrome. The unilobar form, most usually involving the left lobe of the liver, is called Caroli's disease. Both monolobar and diffuse types are often characterised by recurrent bouts of cholangitis and, in over half of the cases, by common bile duct stones without gallbladder stones
Mots-clé
Adult/Aged/Bile Ducts,Intrahepatic/pathology/Caroli Disease/diagnosis/surgery/Cholangiography/Cholecystectomy/Choledochostomy/Cholelithiasis/Common Bile Duct/Female/Hepatectomy/Humans/Male/Middle Aged/Tomography,X-Ray Computed
Pubmed
Open Access
Oui
Création de la notice
18/02/2008 14:30
Dernière modification de la notice
04/04/2023 7:10
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