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  2. Primary sclerosing cholangitis - Wikipedia

    en.wikipedia.org/wiki/Primary_sclerosing_cholangitis

    Primary sclerosing cholangitis and primary biliary cholangitis are distinct entities and exhibit important differences, including the site of tissue damage within the liver, associations with IBD, which includes ulcerative colitis and Crohn's disease, response to treatment, and risks of disease progression. [25]

  3. Cholangiocarcinoma - Wikipedia

    en.wikipedia.org/wiki/Cholangiocarcinoma

    The incidence of cholangiocarcinoma increases with age, and the disease is slightly more common in men than in women (possibly due to the higher rate of primary sclerosing cholangitis, a major risk factor, in men). [47] The prevalence of cholangiocarcinoma in people with primary sclerosing cholangitis may be as high as 30%, based on autopsy ...

  4. Cholestasis - Wikipedia

    en.wikipedia.org/wiki/Cholestasis

    Primary sclerosing cholangitis (PSC) is one of the most common cholestatic liver diseases, yet treatment options remain limited. Treatment for primary biliary cholangitis (PBC) is often done with ursodeoxycholic acid (UDCA) and with no other suitable alternative, it poses a problem for those that are not responsive to (UDCA). However, with ...

  5. Autoimmune pancreatitis - Wikipedia

    en.wikipedia.org/wiki/Autoimmune_pancreatitis

    Changes in the extrapancreatic bile duct similar to those of primary sclerosing cholangitis (PSC) have been reported. [citation needed] The role of endoscopic ultrasound (EUS) and EUS-guided fine-needle aspiration (EUS-FNA) in the diagnosis of AIP is not well described, and EUS findings have been described in only a small number of patients. In ...

  6. Cholangiocyte - Wikipedia

    en.wikipedia.org/wiki/Cholangiocyte

    These diseases include primary biliary cirrhosis, primary sclerosing cholangitis, AIDS cholangiopathy, disappearing bile duct syndromes, Alagille's syndrome, cystic fibrosis, and biliary atresia. Often either the best or the only curative treatment option for cholangiopathies is liver transplantation , and as a group, cholangiopathies account ...

  7. Ursodeoxycholic acid - Wikipedia

    en.wikipedia.org/wiki/Ursodeoxycholic_acid

    WHO Drug Information advises against its use in primary sclerosing cholangitis in unapproved doses beyond 13–15 mg/kg/day. [20] UDCA in a dose of 28–30 mg/kg/day increases risk of death and need for liver transplant by 2.3-fold among those with primary sclerosing cholangitis, despite decrease in liver enzymes. [21]

  8. File:Primary sclerosing cholangitis.webm - Wikipedia

    en.wikipedia.org/wiki/File:Primary_sclerosing...

    What links here; Upload file; Special pages; Printable version; Page information

  9. Secondary sclerosing cholangitis - Wikipedia

    en.wikipedia.org/wiki/Secondary_sclerosing...

    Secondary sclerosing cholangitis (SSC) is a chronic cholestatic liver disease. SSC is a sclerosing cholangitis with a known cause. Alternatively, if no cause can be identified, then primary sclerosing cholangitis is diagnosed. SSC is an aggressive and rare disease with complex and multiple causes.