Pathology of liver Flashcards

(56 cards)

1
Q

True or False.
The liver is very resistant to injury?
Explain

A

= true

Because it has a large functional reserve

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2
Q

What are 3 possible consequences from liver injury?

A

1) severe parenchymal necrosis but heal entirely by restitution
2) Whereas some types of injury leave permanent damage
3) some types of injury produce predictable pathological patterns

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3
Q

describe the pathogenesis of liver disease?

A

1) insult to hepatocytes via viral, drugs, toxins or antibody
2) grading = degrees of inflammation
3) staging = degree of fibrosis
4) cirrhosis

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4
Q

what happens when there is acute liver failure?

A

= acute onset of jaundice

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5
Q

what are 4 causes of acute liver failure?

A
  • viruses
  • alcohol
  • drugs
  • bile duct obstruction
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6
Q

what is a leading cause of acute liver failure and what does this cause?

A

acetaminophen toxicity

  • confluent necrosis producing massive acute necrosis and liver failure
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7
Q

what are 3 possible outcomes of acute liver failure?

A
  • complete recovery
  • chronic liver disease
  • death from liver disease
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8
Q

how do you classify jaundice?

A
  • pre-hepatic
  • hepatic
  • post-hepatic
  • conjugated
  • un-conjugated
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9
Q

what is the cause of pre-hepatic jaundice?

A

= too much haem to break down

  • haemolysis of all causes
  • haemolytic anaemias
  • un-conjugated bilirubin
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10
Q

what is the cause of hepatic jaundice?

A

= liver cells are injured or dead

  • acute liver failure
  • alcoholic hepatitis
  • cirrhosis (decompensated)
  • bile duct loss (atresia, PBC, PSC)
  • pregnancy
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11
Q

what is the cause of post-hepatic jaundice?

A

= bile cannot escape into the bowel

  • congenital biliary atresia
  • gallstones block CBDuct
  • strictures of CBDuct
  • tumours (Ca head of pancreas)
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12
Q

what is cirrhosis?

A

= final common end point for liver disease

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13
Q

Is cirrhosis reversible or irreversible?

A

= irreversible

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14
Q

what is cirrhosis defined by?

A

= bands of fibrosis separating regenerative nodules of hepatocytes
- macro nodular or micro-nodular (alcoholic)

= alteration of hepatic micro-vasculature
= loss of hepatic function

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15
Q

what are 3 complications of cirrhosis?

A

1) portal hypertension (porto-caval anastimoses)
- oesophageal varices
- caput medusa
- haemorrhoids

2) ascites
3) liver failure
4) hepatocellular carcinoma
5) malnutrition

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16
Q

what does the pathology of alcoholic liver disease depend on?

A

= extent of alcohol abuse

= depends upon individual factors

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17
Q

describe the duration of drinking and whether alcoholic liver disease is reversible or irreversible.

A

2-3days = fatty liver
= reversible

4-6weeks = hepatitis
= reversible if drinking stops

Months/years = fibrosis
= irreversible

Years = cirrhosis
= irreversible

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18
Q

in alcoholic fatty liver, i.e. after a weekend bindge, what is the histological appearance of cells?

A

= fat vacuoles appear clear in hepatocytes

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19
Q

in alcoholic hepatitis, i.e. heavy drinking for weeks or months, what is the histological appearance?

A

= hepatocyte necrosis
= neutrophills
= mallory bodies
= pericellular fibrosis

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20
Q

in alcoholic fibrosis, i.e. drinking heavy for months or years, what is the histological appearance?

A

= collagen is layer down around cells

= collagen is stained blue

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21
Q

what is the histological appearance in alcoholic cirrhosis?

A
  • micro-nodular cirrhosis with abundant white scarring
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22
Q

describe non-alcoholic steatohepatitis (NASH)?

A

= non-drinkers but pathology is identical to alcoholic liver disease

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23
Q

who most commonly gets NASH?

A
  • diabetics
  • obese patiens
  • hyperlipidaemia
24
Q

what can NASH lead to?

A
  • fibrosis

- cirrhosis

25
what common virus leads to acute or chronic liver injury?
= viral hepatitis
26
describe hepatitis A-E.
Hep A = Epstein Barr virus Hep B = yellow fever virus Hep C = herpes simplex virus Hep e = cytomegalovirus
27
what is seen histologically with chronic viral hepatitis?
= dense portal chronic inflammation = piecemeal necrosis = lobular inflammation - councilman body - small amounts of steatosis present - fibrosis
28
what are 5 outcomes of hep B?
- fulminant acute infection (death) - chronic hepatitis - cirrhosis - hepato-cellular carcinoma - asymptomatic (carrier)
29
what are 2 outcomes of hep C?
- chronic hepatitis | - cirrhosis
30
what is primary biliary cirrhosis?
= rare auto-immune disease,e unknown cause
31
what is primary biliary cirrhosis associated with?
= auto-antibodies to mitochondria
32
who is most likely to get primary biliary cirrhosis?
= females
33
what is histologically seen in primary biliary cirrhosis?
- chronic portal inflammation - bile ducts inflamed - granuloma around duct
34
describe auto-immune hepatitis?
- more common in females - associated with other AI disease - chronic hepatitis pattern - numerous plasma cells - auto-antibodies to smooth muscle, nuclear or LKM, raised IgG - may have triggers, including some drugs
35
describe chronic drug-induce hepatitis?
- similar to all other chronic hepatitis - may trigger an auto-immune hepatitis - chronic active process
36
what is primary sclerosing cholangitis?
= chronic inflammatory process affecting intra and extra hepatic bile ducts
37
what does primary sclerosing cholangitis lead to?
- leads to peri-ductal fibrosis, duct destruction, jaundice and fibrosis
38
what is primary sclerosing cholangitis associated with?
ulcerative collisi and males
39
what does primary sclerosing cholangittis increase the risk of?
= malignancy in bile ducts and colon
40
what are 3 storage diseases
- haemochromatosis - Wilsons disease - alpha 1 antitrypsin deficiency
41
what is haemochormatosis?
= excess iron within the liver | - iron accumulates in hepatocytes
42
describe primary and secondary haemochormatosis?
primary = genetic condition = increased absorption of iron from small intestine, abnormal iron metabolism secondary = iron overload from diet = transfusions = iron therapy
43
describe the genetics behind primary haemochormatosis?
= inherited autosomal recessive condition - genetic defect v. complex = worse in homozygotes, men
44
describe what happens in primary haemochormatosis?
= iron is deposited into the liver, asymptomatic for years = eventually deposited in portal connective tissue, stimulating fibrosis = cirrhosis if not teated = predisposes to carcinoma = also causes diabetes, cardiac failure and impotence
45
how is the presence of iron confirmed in haemochormatosis?
= Perls stain
46
what is the outcome of haemochormatosis?
= depends on genetics, therapy (venesection) and co-factors like alcohol = cirrhosis = hepatocellular carcinoma
47
what is Wilsons disease?
= inherited autosomal recessive disorder of copper metabolism = copper accumulates in liver and brain (basal ganglia) - low serum caeruuloplasmin
48
what rings appear at Corneal limbus as a result of Wilsons disease?
= Kayser-fleischer
49
what does Wilsons disease cause?
= chronic hepatitis | = neurological deterioration
50
what is alpha-1 antitrypsin deficiency?
= inherited autosomal recessive disorder of production of an enzyme inhibitor = cytoplasmic globules of un-secreted globules of protein in liver cells
51
what does alpha-1 antitrypsin deficiency cause?
= emphysema | = cirrhosis
52
what are 2 types of tumour of the liver?
1) primary (rare) - hepato-cellular adenoma hepato-cellular carcinoma (hepatoma) 2) secondary (common) - multiple = metastases from colon, pancreas, stomach, breast, lung and others
53
is hepatocellular adenoma benign or malignant?
= benign - more common in females
54
what can happen in hepatocellular adenoma?
= may become large and rupture and bleed - most remain asymptomatic
55
what is hepato-cellular carcinoma associated with?
= HBV, HCV and cirrhosis
56
what does hepato-ceellular carcinoma usually present with?
= mass = pain = obstruction