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3,128 Possible Causes for Cirrhosis,, biliary

  • Primary Biliary Cirrhosis

    In many cases, patients die of liver cirrhosis as liver transplant was not done on time.[] Treatment Doctors treat primary biliary cholangitis with medicines.[] Primary biliary cirrhosis is a chronic inflammatory disease of the intrahepatic bile ducts that eventually leads to liver cirrhosis and organ failure, in which several observations[]

  • Cholelithiasis

    Patients with underlying cirrhosis may have coagulopathy, hepatic encephalopathy, ascites and other comorbidities associated with cirrhosis that can make endoscopic therapy[] KEYWORDS: Biliary colic; Cholelithiasis; Gallbladder dyskinesia; Gallstones; Sphincter of Oddi dysfunction[] ,Datong 037003,China; Clinical Significance of Determined Serum Ferritin,Alkaline Phosphatase and Gamma glutamyl transpeptidce in patients with Liver Cirrhosis [J];Anthology[]

  • Biliary Cirrhosis

    Cirrhosis, Biliary/diagnosis Liver Cirrhosis, Biliary/genetics* Liver Cirrhosis, Biliary/immunology* Liver Cirrhosis, Biliary/metabolism Middle Aged Multigene Family Phylogeny[] Primary biliary cirrhosis (PBC) Primary biliary cirrhosis is an autoimmune disease.[] biliary cirrhosis.[]

  • Secondary Biliary Cirrhosis

    Abstract Liver cirrhosis is a diffuse chronic liver disease affecting the entire liver.[] Later she developed secondary biliary cirrhosis with cholangitis due to long stricture of the common bile duct and common hepatic duct requiring biliary stenting.[] HHT has been shown to be associated with intrahepatic biliary stones and might have a causal role.[]

  • Primary Sclerosing Cholangitis

    METHODS: Here we report two cases showing the clinical manifestations of both primary biliary cirrhosis and primary sclerosing cholangitis.[] Primary biliary cirrhosis (PBC) and primary sclerosing cholangitis (PSC)..[] In this report, we attempt to explain the technical details of percutaneous transhepatic cholangiography, percutaneous biliary drainage and percutaneous biliary balloon dilatation[]

  • Progressive Familial Intrahepatic Cholestasis

    The diagnosis of decompensated liver cirrhosis caused by PFIC-3 was finally confirmed by plasma gene detecting.[] CONCLUSION: Regardless of the technique, internal biliary diversion methods are beneficial for the relief of pruritus in PFIC patients.[] CONCLUSIONS: Total biliary diversion can be a useful surgical treatment option for patients with low-GGT PFIC and possibly also Alagille syndrome, when partial biliary diversion[]

  • Ursodiol

    This study aimed to assess the incidence of cirrhosis in UDCA-treated patients with PBC and to determine the predictive factors of cirrhosis development under this treatment[] There is limited information available about the long-term outcome of these patients with primary biliary cirrhosis on UDCA treatment.[] BACKGROUND: Ursodiol (ursodeoxycholic acid) therapy leads to major improvements in patients with primary biliary cirrhosis.[]

  • Secondary Sclerosing Cholangitis

    Liver cirrhosis developed within 12 months. One patient underwent orthotopic liver transplantation. Two patients (50%) died.[] Comprehensive and complete, Blumgart’s Surgery of the Liver, Pancreas and Biliary Tract – edited by Dr. William R.[] Sclerosing cholangitis in critically ill patients is a largely unrecognized new form of SSC, and is associated with rapid progression to liver cirrhosis.[]

  • Cholangitis

    "cirrhosis," which is often inaccurate histologically, as well as having led to stigmatization of some of these patients.[] […] pressure in initiating the process of biliary regurgitation of bacteria, an investigation was made in[] Eight patients, five treated surgically and three who underwent endoscopic biliary drainage, had strictures of the biliary tract.[]

  • Hepatic Sarcoidosis

    During an examination for liver dysfunction, cirrhosis with cholestatic dysfunction and splenomegaly were found.[] […] guidance for all those treating patients with hepato-biliary disease.[] […] cases of sarcoidosis with predominantly hepatic involvement are reported, both with the gradual development of progressive jaundice and other clinical features of primary biliary[]

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