Liver Pathology 2 Flashcards

(59 cards)

1
Q

describe viral hepatitis

A

may cause acute liver injury or chronic liver injury

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2
Q

types of viral hepatitis

A

hep A, B, C, E

delta agent

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3
Q

name of hepatitis A

A

ebstein-barr virus

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4
Q

name of hepatitis B

A

yellow fever virus

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5
Q

name of hepatitis C

A

herpes simplex virus

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6
Q

name of hepatitis E

A

cytomegalovirus

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7
Q

how is hepatitis A spread

A

faecal-oral

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8
Q

describe hepatitis A

A

short incubation period
sporadic or endemic
directly cytopathic
no carrier illness

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9
Q

what is meant by cytopathic

A

refers to structural changes in host cells that are caused by viral invasion
the infecting virus causes lysis of the host cell or when the cell dies without lysis due to an inability to reproduce

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10
Q

recovery from hepatitis A

A

mild illness

usually full recovery

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11
Q

how is hepatitis B spread

A

blood
blood products
sexually
vertically (in utero)

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12
Q

describe hepatitis B

A

long incubation period
liver damage via antiviral immune response
carriers exist

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13
Q

recovery from hepatitis B

A

variable

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14
Q

how is hepatitis c spread

A

blood
blood products
possibly sexually

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15
Q

describe hepatitis C

A

short incubation period
disease waxes and wanes
tends to be chronic

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16
Q

symptoms of hepatitis C

A

often asymptomatic

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17
Q

microscopy of chronic viral hepatitis

A
dense portal chronic inflammation 
interface hepatitis (piecemeal necrosis)
lobular inflammation - councilman body and steatosis 
fibrosis 
cirrhosis
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18
Q

describe interface hepatitis

A

necrosis of the limiting plates, by inflammatory cells

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19
Q

outcomes of hepatitis B

A
fulminant acute infection - death
chronic hepatitis 
cirrhosis 
hepatocellular carcinoma 
asymptomatic (patient becomes a carrier)
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20
Q

outcomes of hepatitis C

A

chronic hepatitis

cirrhosis

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21
Q

aetiology of chronic hepatitis - autoimmune disease

A

primary biliary cirrhosis
autoimmune hepatitis
primary sclerosis cholangitis

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22
Q

aetiology of chronic hepatitis - other causes

A

hep B
hep C
drug induced hepatitis

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23
Q

describe primary biliary cirrhosis

A

rare autoimmune disease

unknown aetiology - associated with autoantibodies to mitochondria

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24
Q

epidemiology of primary biliary cirrhosis

25
pathology of primary biliary cirrhosis
granulomas | bile duct loss
26
out come of primary biliary cirrhosis
unpredictable
27
when would a biopsy be indicated for primary biliary cirrhosis
staging the disease
28
microscopy of primary biliary cirrhosis
chronic portal inflammation bile ducts inflamed granuloma around duct
29
outcomes of primary biliary cirrhosis
if untreated bile duct loss leads to cholestasis liver injury, inflammation, fibrosis and cirrhosis
30
epidemiology of autoimmune hepatitis
females
31
pathology of autoimmune hepatitis
chronic hepatitis pattern numerous plasma cells autoantibodies to smooth muscle, nuclear or LKM, raised IgG
32
epidemiology of autoimmune hepatitis
associated with other autoimmune diseases | may have triggers - including some drugs
33
describe chronic drug-induced hepatitis
similar features to all other types of chronic hepatitis - chronic active process may trigger autoimmune hepatitis
34
describe the effects of drugs on the liver
innumerable drugs can damage liver - may be dose related or idiosyncratic can mimic any liver disease
35
outcomes of drugs on the liver
``` hepatitis granulomas fibrosis necrosis failure cholestasis cirrhosis ```
36
pathology of primary sclerosis cholangitis
chronic inflammatory process affecting intra and extra hepatic bile ducts
37
outcomes of primary sclerosis cholangitis
periductal fibrosis duct destruction jaundice fibrosis increased risk of malignancy in bile ducts and colon
38
epidemiology of primary sclerosis cholangitis
males
39
aetiology of primary sclerosis cholangitis
associated with ulcerative colitis
40
microscopy of primary sclerosis cholangitis
peridcutal onion-skinning fibrosis
41
storage diseases of the liver
haemochromatosis Wilsons disease alpha-1-antitrypsin deficiency
42
what is haemochromatosis
excess iron within the liver | can be primary or secondary
43
primary haemochromatosis
genetic condition - inherited autosomal recessive condition (worse in homozygotes, men) increased absorption of iron
44
secondary haemochromatosis
iron overload from diet transfusion iron therapy
45
pathology of primary haemochromatosis
excess absorption of iron from intestine abnormal iron metabolism iron deposited in liver - asymptomatic for years -deposited in portal connective tissue and stimulates fibrosis
46
outcomes of primary haemochromatosis
``` untreated - fibrosis and cirrhosis predisposes to hepatocellular carcinoma diabetes cardiac failure impotence ```
47
microscopy of haemochromatosis
iron accumulates in hepatocytes - confirmed by Perls stain
48
what is Wilson's disease
inherited autosmal recessive disorder of copper metabolism
49
pathology of Wilson's disease
copper accumulates in liver and brain (basal ganglia) Kasyer-Fleischer rings at corneal limbus low serum caeruloplasmin
50
outcomes of Wilson's disease
chronic hepatitis | neurological deterioration
51
describe alpha-1-antitrypsin deficiency
inherited autosomal recessive disorder of production of an enzyme inhibitor
52
outcomes of alpha-1-antitrypsin deficiency
emphysema | cirrhosis
53
pathology of alpha-1-antitrypsin deficiency
cytoplasmic globes of unsecreted globules of protein in liver cells
54
primary tumours of the liver
rare; hepatocellular adenoma hepatocellular carcinoma (hepatoma)
55
secondary tumours of the liver
common; mutliple metastases from colon, pancreas, stomach, breast, lung...
56
describe hepatoceullar adenoma
bengin seen mostly in females may become large - rupture or bleed may remain asymptomatic
57
describe hepatocellular carcinoma
advanced unless discovered accidentally - poor prognosis | associated with HBV, HCV and cirrhosis
58
symptoms and signs of hepatocellular carcinoma
mass apin obstruction
59
microscopy of hepatocelllar carcinoma
multifocal (rare) hepatocytic cholangio-