Liver Pathology Flashcards

1
Q

How heavy is the liver?

A

1.5 kg

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2
Q

What is the blood supply to the liver?

A

Dual: hepatic artery (20%) and portal vein (80%)

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3
Q

What are the cells of the liver?

A
Hepatocytes
Bile ducts
Blood vessels
Endothelial cells
Kupffer cells
Stellate cells
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4
Q

What is the key parts of the definition of cirrhosis?

A

Whole liver involved
Fibrosis
Nodules of regenerating hepatocytes
Distortion of liver vasculature- intra and extra hepatic shunting of blood

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5
Q

Why are intrahepatic shunts bad?

A

There is unfiltered toxic blood

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6
Q

How do you classify cirrhosis?

A

Nodule size: micronodular vs macronodular

Aetiology: alcoholic/ insulin resistance (more likely to be micronodular)/ viral hepatitis (more likely to be macronodular)

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7
Q

What are the complications of cirrhosis?

A

Portal hypertension (may present with palpable spleen)

Hepatic encephalopathy

Liver cell cancer

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8
Q

What causes acute hepatitis?

A

Viruses

Drugs

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9
Q

What causes chronic hepatitis?

A

Viruses
Drugs
Autoimmune

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10
Q

How do you evaluate chronic hepatitis histology?

A

Severity of inflammation = grade

Severity of fibrosis = stage

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11
Q

What are the stages of ALD?

A

Fatty liver
Alcoholic hepatitis
Cirrhosis

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12
Q

What are the features of alcoholic hepatitis?

A

Ballooning ( +/- Mallory Denk Bodies)
Apoptosis
Pericellular fibrosis
Mainly seen in Zone 3

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13
Q

What is NAFLD?

A

Histologically looks like alcoholic liver disease

Due to insulin resistance associated with raised BMI and diabetes

Becoming recognised as one of the commonest causes of liver disease, world-wide

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14
Q

What is PBC?

A

Previously primary biliary cirrhosis.

F> M

Bile duct loss associated with chronic inflammation (with granulomas)

Diagnostic test is detection of anti-mitochondrial antibodies

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15
Q

What is PSC?

A
M > F
Periductal bile duct fibrosis leading to loss
Associated with ulcerative colitis
Increased risk of cholangiocarcinoma
Diagnostic test is bile duct imaging
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16
Q

What is haemochromatosis?

A

Genetically determined increased gut iron absorption
Gene on chromosome 6 (HFe)
Parenchymal damage to organs secondary to iron deposition (bronzed diabetes)
Prussian blue stain is used to pick out iron

17
Q

What is haemosiderosis?

A

Accumulation of iron in macrophages NOT hepatocytes

No inflammation

Blood transfusion for treatment

18
Q

What is Wilsons disease?

A

Recessive disease (Chromosome 13, heteroallelic): Accumulation of copper due to failure of excretion by hepatocytes into the bile

Assessed by biopsy (Rhodanine stain for copper) or biochemistry

Accumulates in the liver and CNS (hepato-lenticular degeneration) including Kayser-Fleishcer rings

Causes cell damage

19
Q

What is AIH?

A

F>M

Active chronic hepatitis with plasma cells

Anti-smooth muscle actin antibodies in the serum

Responds to steroids

20
Q

What is Alpha 1 Antitrypsin deficiency?

A

Failure to secrete alpha-one antitrypsin

Intra-cytoplasmic inclusions due to misfolded protein

Hepatitis and cirrhosis

Presents in neonatal period with giant cell hepatitis

21
Q

What is DILI?

A

“any kind of liver disease can be caused by a drug” ie. hepatocellular and / or cholestatic

10% of drug reactions involve the liver

Liver is the site for xenometabolism

May be dose-related or idiosyncratic

22
Q

What are hepatic granulomas caused by?

A

Specific causes:
PBC
drugs

General causes:
TB
Sarcoid
Other infective aetiologies etc.

23
Q

What are the benign liver tumours?

A

1) liver cell adenoma
2) bile duct adenoma
3) haemangioma

24
Q

What are the malignant liver tumour classed as?

A
  1. secondary tumours (more common)

2. primary tumours

25
Q

What is the anatomy of the portal venous system?

A

The superior mesenteric vein drains from the gut into the portal vein

The inferior mesenteric vein joins the splenic vein into the portal vein

The short gastric veins, left gastric vein, and umbilical vein drain into the portal vein

The portal veins splits off into the right and left branches then into segmental veins and venules

26
Q

What are the primary liver tumours?

A
  1. hepatocellular carcinoma
  2. hepatoblastoma (primitive hepatocytes-children)
  3. cholangiocarcinoma
  4. haemangiosarcoma (blood vessels)
27
Q

What is liver cell cancer (HCC) associated with?

A

Usually associated with cirrhosis especially in the West.

28
Q

What are the associations of cholangiocarcinomas?

A

Associated with:
PSC
Worm infections
Cirrhosis

Can arise from:
intrahepatic ducts
extrahepatic ducts (including gall bladder)
29
Q

Why are extrahepatic shunts bad?

A

Blood cannot get through liver- porto-systemic anastomoses have increased pressure

30
Q

What is acute hepatitis classes as?

A

<6 months

Chronic > 6 months

31
Q

Are Hepatitis B and C acute or chronic?

A

Both

32
Q

Is alcoholic related fatty change reversible?

A

Yes

33
Q

Where is fibrosis in viral and alcoholic hepatitis?

A
Viral = zone 1
Alcoholic = zone 3
34
Q

How does paracetamol toxicity cause damage?

A

Paracetamol converted to toxic metabolite in the liver and can cause damage

Zone 3 damage (most drug metabolism here)

35
Q

What is a granuloma?

A

Organised collection of activated macrophages