Hepatitis Flashcards

1
Q

what can viral hepatitis be caused by?

A

acute liver injury or chronic liver injury

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2
Q

what are the common and rare causes of viral hepatitis

A
common:
hepA
HepB
HepC
hepE
rare:
delta agent
ebstein-barr virus
yellow fever virus
herpes simplex virus
cytomegalovirus
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3
Q

how is hepA spread and what is its effect on the human

A
faecal-oral spread
short incubation period
sporadic or endemic
directly cytopathic
no carrier state
mild illness, usually full recovery
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4
Q

how is HepB spread

A

spread by blood, blood products, sexually, vertically (in utero)
long incubation period
liver damage is by antiviral immune response
carriers exist
outcome variable

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5
Q

how is hepC spread

A
spread by blood, blood products, possibly sexually
short incubation period
often asymptomatic
disease waxes and wanes
tends to become chronic
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6
Q

how does hepatitis progressively become malignant

A

hepatitis -> inflammation and scarring -> cirrhosis -> hepatocellular carcinoma or liver

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7
Q

what are the outcomes for hepB

A
fulminant acute infection (Death)
chronic hepatitis
cirrhosis
hepatocellular carcinoma
assymptomatic (Carrier)
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8
Q

what are the hepC outcomes

A

chronic hepatitis
cirrhosis
treated and cured

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9
Q

what is the aetiology of chronic hepatitis

A
autoimmune diseases
hepB
hepC
primary biliary cirrhosis
autoimmune hepatitis
drug induced hepatitis
primary sclerosing cholangitis
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10
Q

describe primary biliary cirrhosis

A

rare autoimmune disease, unknown aetiology
associated with autoantibodies to mitochondria
females 90%
indication for biopsy: stage the disease
may see granulomas and bile duct loss
outcome is unpredictable

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11
Q

what does untreated bile duct loss lead to?

A

cholestasis liver injury, inflammation, fibrosis and cirrhosis

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12
Q

describe autoimmune hepatitis

A
commoner in females
associated with other AL disease
chronic hepatitis pattern
numerous plasma cells
autoantibodies to smooth muscle, nuclear or LKM, raised IgG
may have triggers, including some drugs
plasma cells predominate
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13
Q

describe chronic drug-induced hepatitis

A

similar features to the other types of chronic hepatitis
may trigger an autoimmune hepatitis
chronic active process
causes are too many to list

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14
Q

what can drugs do to the liver

A

innumerable drugs can damage the liver
may be dose related or idiosyncratic
can cause hepatitis, granulomas, fibrosis, necrosis, failure, cholestasis or cirrhosis
can mimic any liver disease

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15
Q

what is primary sclerosing cholangitis

A

chronic inflammatory process affecting intra- and extra-hepatic bile ducts

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16
Q

what does primary sclerosing cholangitis lead to

A

leads to periductal fibrosis, duct destruction, jaundice and fibrosis

17
Q

what is primary sclerosing cholangitis associated to

A

ulcerative colitis

18
Q

who does PSC affect and what does it increase the risk of malignancy in?

A

males

bile ducts and colon

19
Q

how does PSC look on histology

A

periductal onion-skinning fibrosis

20
Q

what are the 3 storage diseases

A

haemochromatosis
wilsons disease
alpha-1-antitrypsin deficiency

21
Q

what is haemochromatosis

A

excess iron in liver

22
Q

what is primary haemochromatosis

A
a iron handling/storage disorder
inherited autosomal recessive condition
gene defect v.complex
excess absorbtion of iron from intestine, abnormal iron metabolism
worse in homozygotes, men 
increased absorption of iron
23
Q

what is secondary haemochromatosis

A

iron overload from diet, transfusions, iron therapy

24
Q

what are the outcomes of primary haemochromatosis

A

iron deposited in liver
eventually deposited in portal connective tissue and stimulates fibrosis

cirrhosis if not treated
predisposes to carcinoma
also causes diabetes, cardiac failure and impotence

25
Q

what stain confirms presence of iron in hepatocytes

A

Perls stain

prussian blue

26
Q

what is the outcome for haemochromatosis

A

outcome depends on genetics, therapy (venesection) and cofactors such as alcohol

cirrhosis
hepatocellular carcinoma

27
Q

what is Wilson’s disease

A

inherited autosomal recessive disorder of copper metabolism

28
Q

how does wilsons disease occur

A

copper accumulates in liver and brain (basal ganglia)

29
Q

what are the signs of wilsons disease

A

kayser-fleischer rings at corneal limbus

low serum caeruloplasmin

30
Q

what des wilsons disease cause

A

causes chronic hepatitis and neurological deterioration

31
Q

what is alpha-1-antitrypsin deficiency and what does it cause

A

inherited autosomal recessive disorder of production of an enzyme inhibitor
causes emphysema and cirrhosis

cytoplasmic globules of unsecreted globules of protein in liver cells

32
Q

what are the primary tumours of the liver

A

rare
hepatocellular adenoma
hepatocellular carcinoma (hepatoma)

33
Q

what are the secondary tumours of the liver

A

common multiple

metastases from colon, pancreas, stomach, breast, lung others

34
Q

describe the aetiology of hepatocellular adenoma

A

benign
females
may become large (can rupture or bleed)
most remain assymptomatic

35
Q

describe the aetiology of hepatocellular carcinoma

A

rare in europe
associated with HBV, HCV and cirrhosis due to any cause
fatty liver disease associated with obesity is now one of the commonest
usually presents as a mass, pain, obstruction
usually advanced unless discovered incidentally
poor prognosis

36
Q

what is a malignant primary liver tumour from biliary epithelium called

A

cholangiocarcinoma