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ISSN 1001-5256 (Print)
ISSN 2097-3497 (Online)
CN 22-1108/R
Issue 12
Dec.  2017
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Caroli's syndrome with autosomal dominant polycystic kidney disease:a case report

DOI: 10.3969/j.issn.1001-5256.2017.12.032
  • Published Date: 2017-12-20
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  • [1]CAROLI J, SOUPAULT R, KOSSAKOWSKI J, et al.La dilatation polykystique congenital des voies biliaires intrahepatiques:essai declassification[J].Sem Hop Paris, 1958, 34 (2) :2128-2135.
    [2]DESMET VJ.Congenital diseases of intrahepatic bile ducts:variations on the theme“ductal plate malformation”[J].Hepatology, 1992, 16 (4) :1069-1083.
    [3]SHEN XP, SHEN BX, ZHAO QZ, et al.Diagnosis of Caroli disease by CT and MRI[J].J Chin Physician, 2005, 8 (7) :1045-1047. (in Chinese) 沈新平, 沈比先, 赵清洲, 等.Caroli病的CT和MRI诊断[J].中国医师杂志, 2005, 8 (7) :1045-1047.
    [4]LU N, GUO WL, CHEN LY, et al.CT and MRI diagnosis of Caroli disease (analysis of 8 cases) [J].J Chin Clin Med Imaging, 2006, 11 (17) :656-658. (in Chinese) 陆娜, 郭文力, 陈丽英, 等.Caroli病的影像诊断 (附8例分析) [J].中国临床医学影像杂志, 2006, 11 (17) :656-658.
    [5]PERRICONE G, VANZULLI A.Education and imaging.Hepatology:"central dot sign"of Caroli syndrome[J].J Gastroenterol Hepatol, 2015, 30 (2) :234.
    [6]HUANG ZQ, LIU YX, ZHOU NX.Problems in the surgical treatment of Caroli’s disease[J].Chin J Surg, 1995, 11 (33) :666-668. (in Chinese) 黄志强, 刘永雄, 周宁新.Caroli病外科治疗中的问题[J].中华外科杂志, 1995, 11 (33) :666-668.
    [7]HABIB S, SHAKIL O, COUTO OF, et al.Caroli’s disease and orthotopic liver transplantation[J].Liver Transpl, 2006, 12 (3) :416-421.
    [8]SENYUZ OF, YESILDAG E, KURUOGLU S, et al.Caroli’s disease in children:Is it commonly misdiagnosed?[J].Acta Pediatrica, 2005, 94 (1) :117-120.
    [9]MASYUK AI, MASYUK TV, SPLINTER PL, et al.Cholangiocyte cilia detect changes in luminal fluid flow and transmit them into intracellular Ca2+and c AMP signaling[J].Gastroenterology, 2006, 131 (3) :911-920.
    [10]JORDON D, HARPAZ N, THUNG S.Caroli’s disease and adult polycystic kidney disease:a rarely recognized association[J].Liver, 1989, 9 (1) :30-35.
    [11]DRANSSART M, COGNET F, MOUSSON C, et al.MR cholangiography in the evaluation of hepatic and biliary abnormalities in autosomal dominant polycystic kidney disease:study of 93 patients[J].J Comput Assist Tomogr, 2002, 26 (2) :237-242.
    [12]ISHIKAWA I, CHIKAMOTO E, NAKAMURA M, et al.High incidence of common bile duct dilatation in autosomal dominant polycystic kidney disease patients[J].Am J Kidney Dis, 1996, 27 (3) :321-326.
    [13]TERADA T, NAKAMURA Y.Congenital biliary dilatation in autosomal dominant adult polycystic disease of the liver and kidneys[J].Arch Pathol Lab Med, 1988, 112 (11) :1113-1116.
    [14]WEN J.Congenital hepatic fibrosis in autosomal recessive polycystic kidney disease[J].Clin Transl Sci, 2011, 4 (6) :460-465.
    [15]LIANG JJ, KAMATH PS.Caroli syndrome[J].Mayo Clin Proc, 2013, 88 (6) :e59.
    [16]PARKE, LEE JM, AHN YH, et al.Hepatorenal fibrocystic diseases in children[J].Pediatr Nephrol, 2016, 31 (1) :113-119.
    [17]OBUSEZ EC, UDAYASANKAR U.Autosomal recessive polycystic kidney disease with Caroli syndrome[J].J Urol, 2015, 193 (2) :679-680.
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