MRI for evaluating congenital bile duct abnormalities

Journal of Computer Assisted Tomography

Volumn 26, Issue 4, 2002, Pages 541-552

  Krausé, Denis ^a   Cercueil, Jean Pierre ^a   Dranssart, Marie ^a   Cognet, François ^a   Piard, Françoise ^a   Hillon, Patrick ^a  

^a HÔPITAL DU BOCAGE   (France)

Author keywords

Autosomal dominant polycystic kidney disease (ADPKD); Bile duct atresia; Caroli disease; Congenital bile ducts abnormalities; Hepatic cysts; Magnetic resonance cholangiography (MRCP); MRI

Indexed keywords

BODY FLUIDS; DUCTS; FORESTRY; MAGNETIC RESONANCE;

AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE; AUTOSOMAL DOMINANTS; BILE DUCT ATRESIA; BILE DUCTS; CAROLI DISEASE; CONGENITAL BILE DUCT ABNORMALITY; HEPATIC CYST; MAGNETIC RESONANCE CHOLANGIOGRAPHY; POLYCYSTIC KIDNEY DISEASE;

DIAGNOSIS;

ALAGILLE SYNDROME; ARTICLE; BILE DUCT ATRESIA; BILE DUCT MALFORMATION; CAROLI DISEASE; CHOLANGIOGRAPHY; DIAGNOSTIC ACCURACY; DIFFERENTIAL DIAGNOSIS; EMBRYOLOGY; HAMARTOMA; HEPATOBILIARY SYSTEM; HISTOGENESIS; HUMAN; KIDNEY POLYCYSTIC DISEASE; LIVER FIBROSIS; LIVER POLYCYSTIC DISEASE; MEDICAL ASSESSMENT; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; SCLEROSING CHOLANGITIS;

EID: 0036657318     PISSN: 03638715     EISSN: None     Source Type: Journal    
DOI: 10.1097/00004728-200207000-00013     Document Type: Article

References (36)

1. MR cholangiopancreatography: Potential clinical applications
2. Optimal MR cholangiopancreatographic sequence and its clinical application
3. Cholangiography before biliary surgery: Single-shot MR cholangiography versus intravenous cholangiography
4. Pathogenesis of ductal plate abnormalities
5. MR cholangiopancreatography: Using Haste (Half-Fourier Acquisition Single-Shot Turbo Spin-Echo) sequences
6. Breath hold MR cholangiopancreatography using a Haste sequence: Comparison of single-slice and multislice acquisition techniques
7. Evaluation d'une nouvelle séquence de cholangiographie IRM avec acquisition en demi-plan de Fourier
8. Congenital hepatic fibrosis
9. Association of congenital hepatic fibrosis with autosomal dominant polycystic kidney disease
10. Congenital hepatic fibrosis in autosomal dominant polycystic kidney disease
11. Congenital bile duct cysts. Classification, operative procedures, and review of thirtyseven cases including cancer arising from choledochal cyst
12. Imaging of the choledochal cyst
13. Caroli's disease: Evaluation with MR cholangiopancreatography (MRCP)
14. Imaging findings in Caroli's disease
15. MRI findings in Caroli's disease and intrahepatic pigmented calculi
16. Von Meyenburg complexes of the liver: Imaging findings
17. Bile duct hamartomas (Von Meyenburg complexes) value of MR imaging in diagnosis
18. MRI, CT US and ERCP in the evaluation of bile duct hamartomas (Von Meyenburg complexes): A case report
19. Hepatobiliary cysts in patients with autosomal dominant polycystic kidney disease: Prevalence and CT findings
20. Bile duct calculi in patients with primary sclerosing cholangitis
21. MR cholangiography in primary sclerosing cholangitis
22. Sclerosing cholangitis and biliary tract calculi: Primary or secondary?
23. Primary sclerosing cholangitis MR imaging features
24. Extrarenal manifestations in autosomal dominant polycystic kidney diseases
25. Isolated polycystic liver disease as a distinct genetic disease, unlinked to polycystic kidney disease 1 and polycystic kidney disease
26. Peribiliary cysts associated with severe liver disease: Imaging pathologic correlation
27. Pathological obervations of intrahepatic peri-biliary glands in 1000 consecutive auopsy livers: Survey of necro-inflammation and cystic dilatation
28. Multiple cysts in the hepatic hilum and their pathogenesis: A suggestion of periductal gland origin?
29. Cystic dilatations of peribiliary glands in livers with adult disease and livers with solitary nonparasitic cysts
30. High incidence of common bile duct dilatation in autosomal dominant polycystic kidney disease patients
31. Caroli's disease and adult polycystic kidney disease: A rarely recognized association
32. Caroli's disease and autosomal dominant polycystic kidney disease: A rare association?
33. Cytokeratin immunohistochemical examination of liver: Biopsies in infants with Alagille syndrome and biliary atresia
34. Intrahepatic cholestasis by paucity of interlobular bile ducts in infancy
35. Alagille syndrome today
36. Syndrome of Alagille: Radiological findings and sonographics findings, a review of 37 cases