Primary biliary cirrhosis (PBC) and primary sclerosing cholangitis (PSC) are the two most common and well-characterized primary cholestatic disorders. In contrast to pathologic processes derived primarily from hepatocellular dysfunction, such as viral hepatitis and autoimmune hepatitis, the primary insult in…
The hepatic veno-occlusive diseases are a heterogeneous group of circulatory disorders characterized by obstruction of hepatic venous outflow at the sinusoidal or postsinusoidal levels. These disorders uniquely manifest portal hypertension before overt hepatic parenchymal disease and dysfunction, in contrast to…
Cirrhosis Etiology Virtually any chronic insult to the liver, if sufficiently severe and long-standing, may result in cirrhosis. In the United States, the most common causes are hepatitis C virus (HCV) infection and alcohol ingestion, whereas in Asia and sub-Saharan…
The hepatic storage disorders are genetic conditions characterized by the accumulation of toxic substances within either hepatocytes or the hepatic extracellular matrix. This deposition causes secondary tissue damage, which may eventually progress to cirrhosis, portal hypertension, and hepatocellular carcinoma (HCC).…
Etiology Hepatic iron overload is a generic term that refers to the nonphysiologic accumulation of iron within the hepatic parenchyma. The most clinically significant cause of hepatic iron overload is hereditary hemochromatosis. Hereditary hemochromatosis is associated with several mutations in…
Etiology Fatty liver is a generic term that refers to the accumulation of lipids within hepatocytes. This chapter focuses on nonalcoholic fatty liver disease (NAFLD), the most common form of fatty liver. Histologically, it resembles alcoholic liver injury but occurs…