Congenital cystic diseases of the intra and extrahepatic bile ducts;Lésions kystiques congénitales des voies biliaires intra et extra-hépatiques

Gastroenterologie Clinique et Biologique

Volumn 29, Issue 8-9, 2005, Pages 878-882

  Dhumeaux, Daniel ^a  

^a HENRI MONDOR HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOMAL DOMINANT INHERITANCE; AUTOSOMAL RECESSIVE INHERITANCE; BILE DUCT CYST; BILE DUCT DILATATION; CAROLI DISEASE; CLINICAL FEATURE; COMMON BILE DUCT CYST; CONFERENCE PAPER; DISEASE ASSOCIATION; HISTOPATHOLOGY; HUMAN; KIDNEY MALFORMATION; LIVER CYST; LIVER FIBROSIS; LIVER POLYCYSTIC DISEASE; PORTAL HYPERTENSION; PREVALENCE; RELAPSING POLYCHONDRITIS;

EID: 26244452931     PISSN: 03998320     EISSN: None     Source Type: Journal    
DOI: 10.1016/s0399-8320(05)86364-x     Document Type: Conference Paper

References (30)

1. Desmet VJ. Congenital diseases of intrahepatic bile ducts: variations on the theme "ductal plate malformation". Hepatology 1992;16:1069-83.
2. Desmet VJ. Maladies kystiques du foie: de l'embryologie aux malformations. Gastroenterol Clin Biol 2005;8-9:852-4.
3. Benhamou JP, Menu Y. Non-parasitic cystic diseases of the liver and intrahepatic biliary tree. In: Bircher J, Benhamou JP, McIntyre N, Rizzetto M, Rodés J, eds. Oxford textbook of clinical hepatology. Oxford:Oxord University Press;1999:817-23.
4. th edn. London: Churchill Livingston;2002:107-54
5. th edn. Oxford: Blackwell Scientific Publications 1993:548-61.
6. Summerfield JA, Nagafuchi Y, Sherlock S, Cadafalch J, Scheuer PJ. Hepatobiliary fibropolycystic diseases. A clinical and histological review of 51 patients. J Hepatol 1986;2:141-56.
7. Housset C. Les maladies kystiques du foie. Génétique et biologie cellulaire. Gastroenterol Clin Biol 2005;8-9:855-63.
8. De Koning TJ, Dorland L, van Berge Henegouwen GP. Phosphomannose isomerase deficiency as a cause of congenital hepatic fibrosis and protein-losing enteropathy. J Hepatol 1999;31:557-60.
9. Erlinger S, Sakellaridis DA, Maillard JN, Benhamou JP. Les formes angiocholitiques de la fibrose hépatique congénitale. Presse Med 1969;77:1189-91.
10. Marmorale A, Mainguene C, Gavelli A, Huguet C. Forme angiocholitique pure de la fibrose hépatique congénitale. Gastroenterol Clin Biol 1996;20:211-2.
11. Luciani A, Kobeiter H, Zegai B, Anglade MC, Deux JF, Malhaire C, et al. Maladies fibro-kystiques congénitales du foie: aspects radiologiques. Gastroenterol Clin Biol 2005;8-9:864-8.
12. Lang EK, Macchia RJ, Thomas R, David R, Ruiz-Deya G, Watson RA, et al. Improved detection of renal pathologic features on multiphasic helical CT compared with IVU in patients presenting with microscopic hematuria. Urology 2003;61:528-32.
13. Dupond JL, Miguet JP, Carbillet JP, Saint-Hiller Y, Perol C, Leconte-des-Flory R. Kidney polycystic disease in adult congenital hepatic fibrosis. Ann Intern Med 1978;88:514-5.
14. Chauveau D, Choukroun G, Grünfeld JP. La polykystose hépatorénale autosomique dominante. Med Ther 1995;1:243-51.
15. Caroli J, Corcos V. La dilatation congénitale des voies biliaires intrahépatiques. Rev Med Chir Mal Foie 1964;39:1-70.
16. Boyle MJ, Doyle GD, McNulty JG. Monobar Caroli's disease. Am J Gastroenterol 1989;84:1437-44.
17. Fevery J, Tanghe W, Kerremans R, Desmet V, De Groote J. Congenital dilatation of the intrahepatic bile ducts associated with the development of amyloidosis. Gut 1972;13:604-9.
18. Roudot-Thoraval F, Zafrani ES, Hannoun S, Fagniez PL, Métreau JM, Dhumeaux D. Résection hépatique pour maladie de Caroli limitée au foie gauche. Découverte fortuite d'un cholangiocarcinome. Gastroenterol Clin Biol 1983;7:24-5.
19. Krausé D, Cercueil JP, Dranssart M, Cognet F, Piard F, Hillon P. MRI for evaluating congenital bile duct abnormalities. J Comput Assist Tomogr 2002;26:541-52.
20. Ros E, Navarro S, Bru C, Gilabert R, Bianchi L, Bruguera M. Ursodeoxycholic acid treatment of primary hepatolithiasis in Caroli's syndrome. Lancet 1993;342:404-6.
21. Ramond MJ, Huguet C, Danan G, Rueff B, Benhamou JP. Partial hepatectomy in the treatment of Caroli's disease. Report of a case and review of the literature. Dig Dis Sci 1984;29:367-70.
22. Dagher I, Franco D. Lésions kystiques du foie et des voies biliaires (en dehors du kyste hydatique). Place de la chirurgie. Gastroenterol Clin Biol 2005;8-9:869-71.
23. Everson G, Taylor MRG, Doctor RB. Pokycystic disease of the liver. Hepatology 2004;40:774-82.
24. Wilson PD. Polycystic kidney disease. N Engl J Med 2004;350:151-64.
25. Sherstha R, McKinley C, Russ P, Scherzinger A, Bronner T, Showalter R, et al. Postmenopausal estrogen therapy selectively stimulates hepatic enlargement in women with autosomal dominant polycystic kidney disease. Hepatology 1997;26:1282-6.
26. Swenson K, Seu P, Kinkhabwala M, Maggard M, Martin P, Goss J, et al. Liver transplantation for adult polycystic liver disease. Hepatology 1998;28:412-5.
27. Qian Q, Li A, King BF, Kamath PS, Lager DJ, Huston III J, et al. Clinical profile of autosomal dominant polycystic liver disease. Hepatology 2003;37:164-71.
28. Tahvanainen P, Tahvanainen E, Reijonen H, Halme L, Kääriä inen H, Höckerstedt K. Polycystic liver disease is genetically heterogeneous: clinical and linkage studies in eigth Fnnish families. J Hepatol 2003;38:39-43.
29. Nagorney DM, McIlrath DC, Adson MA. Choledochal cysts in adults: clinical management. Surgery 1984;96:656-63.
30. Voyles CR, Smadja C, Shands WC, Blumgart LH. Carcinoma in choledochal cysts. Age related incidence. Arch Surg 1983;118:986-8.