Literature DB >> 33881897

Diffuse Versus Localized Caroli Disease: A Comparative MRCP Study.

Maïté Lewin1,2, Christophe Desterke2,3, Catherine Guettier2,4, Pierre-Jean Valette5, Hélène Agostini6, Stéphanie Franchi-Abella2,7, Lionel Arrivé8,9, Anita Paisant10, Philippe Petit11, Olivier Soubrane12,13, Didier Samuel2,14, René Adam2,14, Valérie Vilgrain13,15, Benoît Gallix16, Marie-Pierre Vullierme13,15.   

Abstract

OBJECTIVE. The purpose of this multicenter retrospective study was to assess the MRCP features of Caroli disease (CD). MATERIALS AND METHODS. Sixty-six patients were identified from 2000 to 2019. The inclusion criteria were diagnosis of diffuse or localized CD mentioned in an imaging report, presence of intrahepatic bile duct (IHBD) dilatation, and having undergone an MRCP examination. The exclusion criteria included presence of obstructive proximal biliary stricture and having undergone hepatobiliary surgery other than cholecystectomy. Histopathology records were available for 53 of the 66 (80%) patients. Diffuse and localized diseases were compared by chi-square and t tests and Kaplan-Meier model. RESULTS. Forty-five patients had diffuse bilobar CD ((five pediatric patients [three girls and two boys] with a mean [± SD] age of 8 ± 5 years [range, 1-15 years] and 40 adult patients [26 men and 14 women] with a mean age of 35 ± 11 years [range, 20-62 years]) and 21 patients had localized disease (12 men and 9 women; mean age, 54 ± 14 years). Congenital hepatic fibrosis was found only in patients with diffuse CD (35/45 [78%]), as was a "central dot" sign (15/35 [43%]). IHBD dilatation with both saccular and fusiform features was found in 43 (96%) and the peripheral "funnel-shaped" sign in 41 (91%) of the 45 patients with diffuse CD but in none of the patients with localized disease (p < .001). Intrahepatic biliary calculi were found in all patients with localized disease but in only 16 of the 45 (36%) patients with diffuse CD (p < .001). Left liver atrophy was found in 18 of the 21 (86%) patients with localized disease and in none of the patients with diffuse CD (p < .001). The overall survival rate among patients with diffuse CD was significantly lower than that among patients with localized disease (p = .03). CONCLUSION. Diffuse IHBD dilatation with both saccular and fusiform features associated with the peripheral funnel-shaped sign can be used for the diagnosis of CD on MRCP. Localized IHBD dilatation seems to be mainly related to primary intrahepatic lithiasis.

Entities:  

Keywords:  Caroli disease; MRI; bile ducts; congenital lithiasis

Year:  2021        PMID: 33881897     DOI: 10.2214/AJR.20.23522

Source DB:  PubMed          Journal:  AJR Am J Roentgenol        ISSN: 0361-803X            Impact factor:   3.959


  2 in total

Review 1.  Imaging of fibropolycystic liver disease.

Authors:  Kedar Sharbidre; Mohd Zahid; Sudhakar Kundapur Venkatesh; Chandra Bhati; Neeraj Lalwani
Journal:  Abdom Radiol (NY)       Date:  2022-06-07

2.  Childhood-onset Caroli's disease as a cause of recurrent fever: A case report.

Authors:  Jing Sun; Sheng Wang; Biquan Chen
Journal:  Front Pediatr       Date:  2022-08-04       Impact factor: 3.569

  2 in total

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