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  2. Postcholecystectomy syndrome - Wikipedia

    en.wikipedia.org/wiki/Postcholecystectomy_syndrome

    From the gallbladder, bile enters the intestine in individual portions. In the absence of a gallbladder, bile enters the intestine constantly, but in small quantities. Thus, it may be insufficient for the digestion of fatty foods. Postcholecystectomy syndrome treatment depends on the identified violations that led to it.

  3. Cholestasis - Wikipedia

    en.wikipedia.org/wiki/Cholestasis

    Cholestasis arising from TPN has a diverse range of causes, including toxicity to TPN components, underlying disorders, or a lack of enteral nutrition. [47] Without enteral food consumption, gallbladder function is greatly inhibited, leading to gallstone formation, subsequent blockage, and eventually cholestasis. [47]

  4. Cholestatic pruritus - Wikipedia

    en.wikipedia.org/wiki/Cholestatic_pruritus

    Cholestatic pruritus is the sensation of itch due to nearly any liver disease, but the most commonly associated entities are primary biliary cholangitis, primary sclerosing cholangitis, obstructive choledocholithiasis, carcinoma of the bile duct, cholestasis (also see drug-induced pruritus), and chronic hepatitis C viral infection and other forms of viral hepatitis.

  5. Primary biliary cholangitis - Wikipedia

    en.wikipedia.org/wiki/Primary_biliary_cholangitis

    Primary biliary cholangitis (PBC), previously known as primary biliary cirrhosis, is an autoimmune disease of the liver. [1] [2] [3] It results from a slow, progressive destruction of the small bile ducts of the liver, causing bile and other toxins to build up in the liver, a condition called cholestasis.

  6. Progressive familial intrahepatic cholestasis - Wikipedia

    en.wikipedia.org/wiki/Progressive_familial...

    It was previously identified as clinical entities known as Byler's disease and Greenland-Eskimo familial cholestasis. Patients with PFIC-1 may also have watery diarrhea, in addition to the clinical features below, due to FIC-1's expression in the intestine. How ATP8B1 mutation leads to cholestasis is not yet well understood. [citation needed]

  7. The One Thing You Should Never, Ever Do if You Want To Keep ...

    www.aol.com/one-thing-never-ever-want-232500259.html

    Woman with gallbladder pain. Experiencing a gallbladder attack can be summed up in one word: painful. Gallbladder attacks are caused by gallstones (a buildup of bile). The attacks can cause sudden ...

  8. Biliary colic - Wikipedia

    en.wikipedia.org/wiki/Biliary_colic

    [27] Removal of the gallbladder with surgery, known as a cholecystectomy, is the definitive surgical treatment for biliary colic. [28] A 2013 Cochrane review found tentative evidence to suggest that early gallbladder removal may be better than delayed removal. [29] Early laparoscopic cholecystectomy happens within 72 hours of diagnosis. [13]

  9. Neonatal cholestasis - Wikipedia

    en.wikipedia.org/wiki/Neonatal_cholestasis

    Most children will also require a liver transplant in the future because they will progress to having cirrhosis, hepatocellular carcinoma, and/or chronic liver disease. [13] Generally, treatment of neonatal cholestasis involves treating the underlying disease. Prognosis of neonatal cholestasis also varies based on the underlying pathologic process.