Podcast
Questions and Answers
What is the primary histological feature that defines chronic viral hepatitis?
What is the primary histological feature that defines chronic viral hepatitis?
- Spotty necrosis in hepatocytes
- Hepatocyte apoptosis
- Fibrous septa in portal tracts
- Mononuclear portal infiltration (correct)
What histological pattern is associated with interface hepatitis in chronic liver conditions?
What histological pattern is associated with interface hepatitis in chronic liver conditions?
- Infiltration at the portal tract stroma (correct)
- Inflammation within portal tracts
- Necrosis of hepatocytes
- Destruction of hepatocyte parenchyma
Which cell type is identified by swollen endoplasmic reticulum due to HBsAg in chronic hepatitis B?
Which cell type is identified by swollen endoplasmic reticulum due to HBsAg in chronic hepatitis B?
- Lymphocytes
- Ground-glass hepatocytes (correct)
- Kupffer cells
- Fibroblasts
In advanced cases of chronic liver damage, what key feature develops alongside increasing scarring?
In advanced cases of chronic liver damage, what key feature develops alongside increasing scarring?
What characterizes autoimmune hepatitis in relation to its demographic prevalence?
What characterizes autoimmune hepatitis in relation to its demographic prevalence?
Which test is considered the most sensitive and accurate for diagnosing Wilson disease?
Which test is considered the most sensitive and accurate for diagnosing Wilson disease?
What is a characteristic ocular finding in patients with neurologic involvement of Wilson disease?
What is a characteristic ocular finding in patients with neurologic involvement of Wilson disease?
In Wilson disease, what region of the brain is primarily affected by toxic injury?
In Wilson disease, what region of the brain is primarily affected by toxic injury?
What describes the inheritance pattern of α1-Antitrypsin deficiency?
What describes the inheritance pattern of α1-Antitrypsin deficiency?
What is the primary cause of ascites in 85% of cases?
What is the primary cause of ascites in 85% of cases?
What is a key biochemical marker indicating α1-Antitrypsin deficiency?
What is a key biochemical marker indicating α1-Antitrypsin deficiency?
Which clinical sign is characteristic of hepatic encephalopathy?
Which clinical sign is characteristic of hepatic encephalopathy?
What is the major role of the hepatitis D virus (HDV)?
What is the major role of the hepatitis D virus (HDV)?
What characterizes the fluid accumulation in ascites?
What characterizes the fluid accumulation in ascites?
Which of the following is NOT a major clinical consequence of portal hypertension?
Which of the following is NOT a major clinical consequence of portal hypertension?
What is the main neurological disturbance associated with hepatic encephalopathy?
What is the main neurological disturbance associated with hepatic encephalopathy?
In acute viral hepatitis, the portal inflammation is typically characterized as:
In acute viral hepatitis, the portal inflammation is typically characterized as:
What is a common clinical presentation in hepatic encephalopathy?
What is a common clinical presentation in hepatic encephalopathy?
What is marked by plasma cell predominance in the mononuclear inflammatory infiltrates?
What is marked by plasma cell predominance in the mononuclear inflammatory infiltrates?
What initiates all changes in alcoholic liver disease?
What initiates all changes in alcoholic liver disease?
Which of the following statements regarding hepatocellular steatosis is true?
Which of the following statements regarding hepatocellular steatosis is true?
What typically signifies the presence of alcoholic hepatitis?
What typically signifies the presence of alcoholic hepatitis?
Which is a major consequence of alcoholic (steato-) hepatitis?
Which is a major consequence of alcoholic (steato-) hepatitis?
Which structures are typically associated with alcoholic liver disease?
Which structures are typically associated with alcoholic liver disease?
What condition is primarily caused by excessive ethanol consumption?
What condition is primarily caused by excessive ethanol consumption?
What happens to lipid droplets in hepatocytes over time with chronic alcohol intake?
What happens to lipid droplets in hepatocytes over time with chronic alcohol intake?
What is a characteristic feature of macrovesicular steatosis?
What is a characteristic feature of macrovesicular steatosis?
Which of the following is NOT a common cause of cirrhosis?
Which of the following is NOT a common cause of cirrhosis?
What complication is primarily associated with portal hypertension?
What complication is primarily associated with portal hypertension?
Which symptom is specifically related to impaired liver function?
Which symptom is specifically related to impaired liver function?
What is a potential outcome of fully established cirrhosis?
What is a potential outcome of fully established cirrhosis?
Which of the following laboratory findings is typically associated with liver failure?
Which of the following laboratory findings is typically associated with liver failure?
Which of the following conditions is a major cause of post-hepatic portal hypertension?
Which of the following conditions is a major cause of post-hepatic portal hypertension?
Which symptom is indicative of impaired estrogen metabolism in liver disease?
Which symptom is indicative of impaired estrogen metabolism in liver disease?
What characterizes the pattern of perisinusoidal scarring in fibrosis?
What characterizes the pattern of perisinusoidal scarring in fibrosis?
What is a classic morphological hallmark of hemochromatosis?
What is a classic morphological hallmark of hemochromatosis?
What primarily causes Wilson disease?
What primarily causes Wilson disease?
Which condition is characterized by the presence of micronodular cirrhosis?
Which condition is characterized by the presence of micronodular cirrhosis?
Which of the following statements regarding Wilson disease is true?
Which of the following statements regarding Wilson disease is true?
What is a notable feature of alcoholic cirrhosis?
What is a notable feature of alcoholic cirrhosis?
What is the primary disorder in hemochromatosis?
What is the primary disorder in hemochromatosis?
Which of these organs is NOT commonly affected by copper accumulation in Wilson disease?
Which of these organs is NOT commonly affected by copper accumulation in Wilson disease?
Flashcards
Microvesicular steatosis
Microvesicular steatosis
Accumulation of multiple small fat droplets within liver cells, not displacing the nucleus.
Macrovesicular steatosis
Macrovesicular steatosis
Accumulation of a single large fat droplet within liver cells, displacing the nucleus.
Cirrhosis
Cirrhosis
Advanced scarring of the liver, characterized by fibrous bands subdividing it into regenerative nodules.
Liver failure
Liver failure
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Portal hypertension
Portal hypertension
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Ascites
Ascites
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Splenomegaly
Splenomegaly
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Esophageal varices
Esophageal varices
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Hepatocyte injury
Hepatocyte injury
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Mononuclear portal infiltration
Mononuclear portal infiltration
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Interface hepatitis
Interface hepatitis
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Liver scarring
Liver scarring
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Ground-glass hepatocytes
Ground-glass hepatocytes
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What is portal hypertension?
What is portal hypertension?
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What is ascites?
What is ascites?
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What is hepatic encephalopathy?
What is hepatic encephalopathy?
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What are esophageal varices?
What are esophageal varices?
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What is splenomegaly?
What is splenomegaly?
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What is Hepatitis D Virus?
What is Hepatitis D Virus?
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What is Hepatitis E Virus?
What is Hepatitis E Virus?
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What is Hepatitis C Virus?
What is Hepatitis C Virus?
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Alpha-1-Antitrypsin Deficiency
Alpha-1-Antitrypsin Deficiency
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Wilson Disease
Wilson Disease
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Kayser-Fleischer Rings
Kayser-Fleischer Rings
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Hepatic Copper Content
Hepatic Copper Content
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Urinary Copper Excretion
Urinary Copper Excretion
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Hepatic Steatosis (Fatty Liver)
Hepatic Steatosis (Fatty Liver)
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Alcoholic (Steato-) Hepatitis
Alcoholic (Steato-) Hepatitis
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Mallory-Denk Bodies
Mallory-Denk Bodies
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Alcoholic Steatofibrosis
Alcoholic Steatofibrosis
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Alcoholic Liver Disease
Alcoholic Liver Disease
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Activation of Stellate Cells and Portal Fibroblasts
Activation of Stellate Cells and Portal Fibroblasts
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Hepatocyte Swelling and Necrosis
Hepatocyte Swelling and Necrosis
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Neutrophilic Reaction
Neutrophilic Reaction
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Hemochromatosis: What is it?
Hemochromatosis: What is it?
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Micronodular Cirrhosis: What is it?
Micronodular Cirrhosis: What is it?
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Chicken Wire Fence Pattern: What is it?
Chicken Wire Fence Pattern: What is it?
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Perisinusoidal Scarring: What is it?
Perisinusoidal Scarring: What is it?
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Wilson Disease: What is it?
Wilson Disease: What is it?
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Copper Accumulation in Wilson Disease: What is it?
Copper Accumulation in Wilson Disease: What is it?
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Hemosiderin Granules: What are they?
Hemosiderin Granules: What are they?
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Fibrosis in the Liver: How does it occur?
Fibrosis in the Liver: How does it occur?
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Study Notes
Liver Anatomy
- The liver is 1400-1600 gm in adults.
- It has a dual blood supply: portal vein (60-70%) and hepatic artery (30-40%).
- Portal tracts contain portal veins, hepatic arteries, and bile ducts.
- The liver is divided into lobules (1-2 mm).
- Lobules are oriented around the terminal hepatic veins.
- Portal tracts are at the periphery of lobules.
- Hepatocytes are organized into sheets or plates.
- Vascular sinusoids are between the plates.
- Space of Disse is beneath endothelial cells.
- Kupffer cells are in the space of Disse.
- Myofibroblastic hepatic stellate cells also reside in the space of Disse.
Liver Histology
- Liver lobules are 1-2 mm in diameter.
- Hepatic architectural structures are based on a lobular model.
- The portal vein branches, hepatic arteries and bile ducts travel in parallel.
- Hepatocytes near the terminal hepatic vein are centrilobular, and those near the portal tract are periportal.
- Hepatocytes are organized into anastomosing sheets or plates, extending from portal tracts to terminal hepatic veins.
- Vascular sinusoids separate the plates.
- The space of Disse contains stellate cells (mononuclear phagocyte system) and is beneath endothelial cells.
Liver Acinus
- A functional unit of the liver from a metabolic perspective.
- Centered on the line connecting two portal triads.
- Extends outward to the two adjacent central veins.
Liver Cords and Sinusoids
- Hepatocytes are organized into cords that are separated by sinusoids.
- Blood-filled sinusoids contain blood, Kupffer cells, and the space of Disse.
- Hepatocytes line the sinusoids.
- Stellate cells reside in the space of Disse.
- Endothelial cells line the sinusoid lumen.
Normal Liver Structure
- Histologically divided into lobules.
- Functionally divided into 3 zones, based on oxygen supply.
- Zone 1 encircles portal triads - oxygenated blood from hepatic arteries enters.
- Zone 3 surrounds the central vein - poor oxygenation.
- Zone 2 is between Zone 1 and Zone 3.
Portal Triad
- Interlobular connective tissue. Branch of the portal vein, hepatic artery, and bile duct.
Liver H&E Staining
- Basic histological staining procedure for visualization of specific features.
Liver Histology Micrographs
- Microscopic images of stained liver tissue.
- Portal vein, hepatic artery, and bile duct identification.
- Connective tissue interface.
Gross Images
- Visual representations of liver with cirrhosis, showing nodules of fat.
Microscopic Description
- Diffuse disruption in the liver architecture.
- Bridging fibrous septa.
- Roundish parenchymal nodules of regenerating hepatocytes.
Interface Hepatitis
- Inflammation between inflamed portal tracts and periportal parenchyma.
- Inflammatory cells.
- Portal tracts and periportal parenchyma.
Giant Cell Transformation
- Hepatocytes with 6 or more nuclei.
Mallory Hyaline
- Irregular, rope-like inclusions of cytokeratin.
- Often seen in ballooning cells (alcoholism).
Microvesicular Steatosis
- Multiple tiny intracytoplasmic fat droplets that do not displace the nucleus.
Macrovesicular Steatosis
- Single large intracytoplasmic fat droplet which displaces the nucleus.
Cirrhosis
- Diffuse nodulation of liver due to fibrous bands.
- Fibrous bands divide liver into regenerative nodules.
- Common causes include chronic viral hepatitis, fatty liver disease, autoimmune hepatitis, primary biliary cholangitis, and drug-induced liver injury.
- Chronic cirrhosis can regress.
Child-Pugh Classification
- Scoring system for assessing severity of cirrhosis.
- Factors such as bilirubin, albumin, prothrombin time, and encephalopathy are measured and scored to determine a class, from A (less severe) to C (more severe).
- Used to determine the appropriate treatment, such as transplantation.
Hepatocyte and Parenchymal Responses
- Necrosis of hepatocytes, due to cluster of macrophages—indicating tissue damage.
- Acidophil bodies are seen after cell death; they represent debris from hepatocytes.
- Councilman bodies (acidophilic bodies) represent single cell death.
Ballooning (Feathery) Degeneration
- Hepatocyte swelling with increased pale cytoplasm.
Bridging Necrosis
- Necrotic cells span adjacent lobules.
Centrilobular Necrosis
- Necrotic hepatocytes around central vein.
- Usually result from ischemia, drugs, or toxins.
Portal Hypertension
- Increased resistance to portal blood flow.
- Prehepatic, intrahepatic, or post-hepatic conditions are obstructive thrombosis, severe right-sided heart failure, constrictive pericarditis, or hepatic vein outflow obstruction.
- Four consequences include ascites, portosystemic venous shunts, congestive splenomegaly, and hepatic encephalopathy.
Ascites
- Accumulation of excess fluid in the peritoneal cavity.
Hepatic Encephalopathy
- Spectrum of disturbances in consciousness.
- Fluctuations in neurological signs (rigidity and hyperreflexia).
- Asterixis (nonrhythmic, rapid extension-flexion movements).
- Disorder of neurotransmission in the central nervous system.
- Elevated ammonia correlates with impaired neuronal function.
Hepatitis A, B, C, D, E Viruses
- Different viruses that cause liver inflammation (hepatitis).
- Routes of transmission, symptoms, prevention, and typical outcomes (acute or chronic).
a₁-Antitrypsin Deficiency
- Autosomal recessive disorder of protein folding.
- Low levels of circulating a₁-antitrypsin.
- Inhibition of proteases (neutrophil elastase, cathepsin G, and proteinase 3).
- Pulmonary emphysema and liver disease.
- Cytoplasmic, globular inclusions in hepatocytes.
Wilson's Disease
- Autosomal recessive disorder of copper metabolism.
- Defective ATP7B gene leads to impaired copper excretion.
- Copper accumulates in the liver, brain, and eyes.
- Kayser-Fleischer rings are a hallmark diagnostic finding from copper accumulation in the eyes.
Alcoholic Liver Disease
- Excessive alcohol consumption is the leading cause.
- Three distinctive forms of alcoholic liver injury:
- Hepatocellular steatosis.
- Alcoholic hepatitis.
- Steatofibrosis.
- These forms are overlapping, and can transition into each other as the disorder progresses.
Alcoholic Steatofibrosis
- Chronic alcoholic hepatitis is accompanied by prominent activation of sinusoidal stellate cells and portal fibroblasts resulting in fibrosis.
Interface Hepatitis ("Piecemeal Necrosis")
- Inflammation at the interface between the connective tissue and liver parenchyma.
- Severity classified according to how widely the inflammation spreads or the proportion of involved portal tracts (focal or diffuse).
Hemochromatosis
- Excessive iron absorption causing iron deposition in parenchymal organs.
- Golden-yellow hemosiderin granules in the hepatocytes.
- Micronodular cirrhosis.
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Description
Test your knowledge on the histological features and patterns associated with chronic viral hepatitis and autoimmune hepatitis. This quiz covers critical aspects such as interface hepatitis, cellular changes, and demographic prevalence. Perfect for students and professionals in the field of hepatology.