Liver Pathology Flashcards

1
Q

What are the normal functions of the liver?

A

Storage

  • glycogen
  • vitamins
  • iron
  • copper

Synthesis

  • glucose
  • protein
  • lipids & cholesterol
  • bile
  • coagulation factors
  • albumin

Metabolism

  • bilirubin
  • ammonia
  • drugs
  • alcohol
  • carbohydrate/lipids
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2
Q

What is cirrhosis?

A

Irreversible scarring of the liver

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3
Q

What happens to the liver in cirrhosis?

A

Ongoing inflammation
Fibrosis
Hepatocyte necrosis

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4
Q

What is the end result of cirrhosis?

A

Impairment of liver function

Vascular changes - portal hypertension

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5
Q

What can cause cirrhosis?

A

Drugs

  • alcohol
  • iatrogenic

Infection

  • hep b
  • hep c

Deposition

  • fat
  • iron
  • copper

Autoimmune

  • hepatitis
  • primary biliary cirrhosis
  • primary sclerosing cholangitis

Other

  • α1 antitrypsin
  • glycogen storage disease
  • budd-chiari disease
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6
Q

What are 3 main mechanisms alcohol can affect the liver?

A

Fatty change
Alcoholic hepatitis
Cirrhosis

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7
Q

What are the signs of fatty liver?

A

Hepatomegaly

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8
Q

Is fatty liver reversible?

A

Yes

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9
Q

What are the signs of alcoholic hepatitis?

A

Rapid onset jaundice
Tender hepatomegaly
Nausea
Oedema

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10
Q

Is alcoholic hepatitis reversible?

A

Yes initially

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11
Q

Does hepatitis B have a vaccine?

A

Yes

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12
Q

Does hepatitis B have a cure?

A

No

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13
Q

Does hepatitis C have a vaccine?

A

No

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14
Q

Does hepatitis C have a cure?

A

Yes

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15
Q

What is non-alcoholic liver disease?

A

Accumulation of triglycerides in hepatocytes - causes similar pathogensis to ALD

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16
Q

What is hereditary haemochromatosis?

A

Abnormal iron metabolism

17
Q

What is the inheritance pattern of hereditary haemochromatosis?

A

Autosomal recessive

18
Q

What is the effect of hereditary haemochromatosis?

A

Increased absorption of iron
- excess deposition

Elevated serum iron
Abnormal LFTs

19
Q

How is hereditary haemochromatosis managed?

A

Venesection

20
Q

What is Wilson’s disease?

A

Abnormal copper metabolism

21
Q

What is the inheritance pattern of Wilson’s disease?

A

Autosomal recessive

22
Q

What is the effect of Wilson’s disease?

A

Reduced secretion of copper from biliary system

- accumulates in tissues

23
Q

What is a sign of Wilson’s disease?

A

Kayser-Fleischer ring around iris

24
Q

How is Wilson’s disease managed?

A

Chelating agents

Zinc

25
What is primary sclerosing cholangitis?
Fibrosis of intra and extra hepatic bile ducts
26
Who is more commonly affected by primary sclerosing cholangitis?
Men
27
What are the symptoms of primary sclerosing cholangitis?
Asymptomatic Pruritus Cholangitis Jaundice
28
Which antibody is present in primary sclerosing cholangitis?
ANCA
29
What is primary biliary cirrhosis?
Destruction of intrahepatic bile ducts
30
Who is more commonly affected by primary biliary cirrhosis?
Women
31
What are the symptoms of primary biliary cirrhosis?
Asymptomatic Pruritus +/- jaundice
32
What antibody is present in primary biliary cirrhosis?
AMA
33
What is portal hypertension?
Build up of blood in the portal venous system
34
What cause portal hypertension?
Fibrotic liver - No very expandable - compresses veins entering liver - increased hydrostatic pressure in portal system
35
What are the effects of portal hypertension?
Ascites - increased hydrostatic pressure Varices - shunt from portal to systemic system
36
What are the common sites of varices?
Oesophageal Umbilical Anorectal
37
What are umbilical varices also known as?
Caput medusa
38
What is hepatorenal syndrome?
Development of AKI in the presence of cirrhosis
39
How does hepatorenal syndrome occur?
Portal hypertension Arterial vasodilation - splanchnic artery RAAS activated Renal artery vasoconstriction