Liver, Gallbladder, and Pancreas Diseases

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Comprehensive vocabulary flashcards reviewing the anatomical, physiological, pathological, and diagnostic concepts of liver, biliary tree, and pancreatic diseases.

Last updated 2:52 PM on 10/15/26
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31 Terms

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Dual Blood Supply of the Liver

The vascular inflow system supplying the liver (which weighs 1.4–1.6 kg1.4\text{--}1.6\,\text{kg}), consisting of both the hepatic artery and portal vein.

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Steatosis

The abnormal accumulation of toxic fatty products within hepatocytes as a cellular response to liver injury.

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Cholestasis

The systemic or hepatic accumulation of bilirubin and other bile solutes resulting from impaired bile secretion or obstruction of bile flow.

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Serum Aminotransferases (AST and ALT)

Cytosolic hepatocellular enzymes whose serum elevation indicates acute hepatocyte damage resulting from ischemia, toxic exposure, or viral hepatitis.

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AST:ALT Ratio in Cirrhosis

A laboratory ratio that may become >1>1 because cytosolic ALT leaks easily upon early damage, whereas mitochondrial AST is released as hepatocytes undergo complete cellular destruction and are replaced by fibrous scar tissue.

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Alkaline Phosphatase (ALP) and GGT

Plasma membrane enzymes located in the bile canaliculus whose elevation in the blood specifically signifies biliary canalicular damage and obstruction of bile flow.

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Direct Bilirubin Elevation

A high concentration of water-soluble conjugated bilirubin in the serum, which indicates that the liver is functionally conjugating bilirubin but an obstruction to bile excretion is present.

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<p>Jaundice (Icterus)</p>

Jaundice (Icterus)

Yellow discoloration of tissue caused by excess serum bilirubin levels exceeding >2.0 mg/dL>2.0\,\text{mg/dL}; hemolytic anemias represent the number one cause worldwide.

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<p>Cirrhosis</p>

Cirrhosis

A severe end-stage liver condition characterized morphologically by diffuse, nodular regeneration bounded by bridging fibrous septa; it ranks among the top 10 causes of adult death in the US.

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<p>Ascites</p>

Ascites

The accumulation of serous fluid within the peritoneal cavity caused by portal hypertension, decreased albumin synthesis, and altered vascular pressures in cirrhosis.

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<p>Esophageal Varices</p>

Esophageal Varices

Dilated collateral veins forming in the submucosa of the esophagus due to portal hypertension that bypass the scarred liver to reach the caval system, presenting a severe risk of fatal rupture.

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<p>Spider Angiomas</p>

Spider Angiomas

Vascular skin lesions characterized by central arterioles with radiating capillaries that develop in patients with chronic liver failure and cirrhosis.

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Hepatitis A Virus (HAV)

A benign, self-limited RNA virus transmitted via the fecal-oral route through contaminated food and water, having an incubation period of 2–6 weeks2\text{--}6\,\text{weeks} and no chronic disease or carrier state.

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Hepatitis B Virus (HBV)

A parenteral and sexually transmitted DNA virus with an incubation period of 4–26 weeks4\text{--}26\,\text{weeks}; roughly 90%90\% of cases resolve spontaneously while 5%–10%5\%\text{--}10\% progress to chronic hepatitis.

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Hepatitis C Virus (HCV)

An RNA virus spread by parenteral or sexual contact that progresses to chronic hepatitis in 85%85\% of cases due to genomic instability, which also precludes vaccine development.

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Fulminant Hepatitis

A severe form of acute hepatitis defined by massive hepatocyte necrosis leading rapidly to acute liver failure, often requiring liver transplantation to avoid death.

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Chronic Hepatitis

Hepatic inflammation associated with abnormal liver function persisting for >6 months>6\,\text{months}, histologically characterized by portal tract inflammation and progressive fibrosis.

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Alcoholic Liver Disease

A spectrum of alcohol-induced hepatic disorders accounting for 60%60\% of chronic liver disease, manifesting in three main features: hepatic steatosis, alcoholic hepatitis, and cirrhosis.

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Mallory Bodies

Eosinophilic cytoplasmic inclusions within degenerating hepatocytes seen characteristically in the setting of alcoholic hepatitis.

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Hemochromatosis

An autosomal recessive genetic disorder linked to the HFE gene on chromosome 6 that disrupts hepcidin regulation, leading to excessive iron absorption and toxic deposition of hemosiderin in the liver, pancreas, and heart.

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Wilson's Disease

An autosomal recessive disorder characterized by the toxic accumulation of copper within the liver, brain, and eyes.

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Hepatocellular Adenoma

A benign liver tumor composed of bland hepatocytes lacking bile ducts, associated with oral contraceptive use, which can present as an acute abdomen secondary to intra-abdominal hemorrhage.

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Hepatocellular Carcinoma (HCC)

The most common primary malignant tumor of hepatocytes, displaying a 3:13:1 male predominance, strong correlation with cirrhosis (90%90\%), HBV, HCV, and aflatoxin, and a high propensity for vascular invasion.

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Cholangiocarcinoma

An aggressive adenocarcinoma arising from bile duct epithelium inside or outside the liver, commonly remaining asymptomatic until late stages.

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<p>Cholesterol Gallstones</p>

Cholesterol Gallstones

The most common form of cholelithiasis in Western populations (80%80\%), primarily radiolucent, and associated with Caucasian ethnicity, advanced age, female sex, and elevated estrogen levels.

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<p>Pigment Gallstones</p>

Pigment Gallstones

Gallstones composed primarily of bilirubin salts (20%20\% in the West) that are mostly radiopaque and linked to chronic hemolysis, gastrointestinal disorders, and biliary infections.

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Acute Cholecystitis

Acute inflammation of the gallbladder presenting with severe right upper quadrant (RUQ) abdominal pain, often triggered by cystic duct obstruction, ischemia, or chemical irritation.

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Gallbladder Carcinoma

An adenocarcinoma representing the 5th most common gastrointestinal malignancy, with a peak in the 7th decade, a higher prevalence in females, a 95%95\% association with gallstones, and a 5-year survival rate of only 5%5\%.

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Acute Pancreatitis

Reversible acute inflammatory injury of the pancreas driven by autodigestion via activated lipases and proteases, vascular destruction with hemorrhage, and localized fat necrosis, with 80%80\% of cases caused by gallstones or alcohol abuse.

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Chronic Pancreatitis

Progressive, irreversible destruction of the exocrine pancreatic parenchyma followed by loss of endocrine islets and extensive fibrosis, commonly caused by long-term alcoholism.

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Pancreatic Ductal Carcinoma

A malignant exocrine neoplasm (mostly adenocarcinoma) ranking as the 4th leading cause of US cancer deaths; it exhibits silent growth and poor prognosis, with smoking doubling disease risk.