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  2. Zieve's syndrome - Wikipedia

    en.wikipedia.org/wiki/Zieve's_syndrome

    Zieve's syndrome is an acute metabolic condition that can occur during withdrawal from prolonged heavy alcohol use. It is defined by hemolytic anemia (with spur cells and acanthocytes), hyperlipoproteinemia (excessive blood lipoprotein), jaundice (elevation of unconjugated bilirubin), and abdominal pain. [1]

  3. Hepatorenal syndrome - Wikipedia

    en.wikipedia.org/wiki/Hepatorenal_syndrome

    The development of ascites (as shown on this abdominal ultrasound) in cirrhotics that is refractory to the use of diuretic medications is associated with type 2 HRS. Hepatorenal syndrome is a particular and common type of kidney failure that affects individuals with liver cirrhosis or, less commonly, with fulminant liver failure. [1]

  4. Cirrhosis - Wikipedia

    en.wikipedia.org/wiki/Cirrhosis

    Cirrhosis, also known as liver cirrhosis or hepatic cirrhosis, chronic liver failure or chronic hepatic failure and end-stage liver disease, is a condition of the liver in which the normal functioning tissue, or parenchyma, is replaced with scar tissue and regenerative nodules as a result of chronic liver disease.

  5. Budd–Chiari syndrome - Wikipedia

    en.wikipedia.org/wiki/Budd–Chiari_syndrome

    It is generally reserved for patients with fulminant liver failure, failure of shunts, or progression of cirrhosis that reduces the life expectancy to one year. [23] Survival rates in Budd–Chiari syndrome after liver transplantation are 76%, 71% and 68% after 1, 5 and 10 years respectively. [2]

  6. Autoimmune hepatitis - Wikipedia

    en.wikipedia.org/wiki/Autoimmune_hepatitis

    Liver cirrhosis can develop in about 7% to 40% of treated patients. People with the highest risk for progression to cirrhosis are those with incomplete response to treatment, treatment failure, and multiple relapses. Once cirrhosis develops, management of liver cirrhosis in autoimmune hepatitis is standard regardless of etiology.

  7. Hepatolithiasis - Wikipedia

    en.wikipedia.org/wiki/Hepatolithiasis

    Accurately identifying stones, biliary strictures, and affected liver segments is crucial for the diagnosis of hepatolithiasis, as is ruling out concurrent cholangiocarcinoma. [2] Hepatolithiasis is primarily diagnosed by abdominal ultrasonography (USG) and computed tomography (CT) scans. [3]

  8. Portal vein thrombosis - Wikipedia

    en.wikipedia.org/wiki/Portal_vein_thrombosis

    Cirrhosis alters bleeding pathways thus patients are simultaneously at risk of uncontrolled bleeding and forming clots. [3] A long-standing hindrance in flow as in chronic PVT, also known as portal cavernoma, can cause an increase in the hepatic venous pressure gradient ( portal hypertension ) and increased blood flow through subsidiary veins ...

  9. Portal hypertensive gastropathy - Wikipedia

    en.wikipedia.org/wiki/Portal_hypertensive_gastro...

    Portal hypertensive gastropathy refers to changes in the mucosa of the stomach in patients with portal hypertension; by far the most common cause of this is cirrhosis of the liver. These changes in the mucosa include friability of the mucosa and the presence of ectatic blood vessels at the surface.