Liver disease Flashcards

1
Q

what is jaundice and the different types

A

visible in white of eye - abnomrmialty of metabolism of bilirubin >40umol/L
most common sign of lier disease
pre hepatic - too much produced
hepatic - too few functioning liver cells
post hepatic - bile duct obstruction

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2
Q

what are the various causes of jaundice and the effect on appearance

A

pre hepatic - haemolytic anaemia, gilberts syndrome (enzyme deficiency), unconjugated and bound to albumin = yellow skin

hepatic - onstage liver disease, mainly conjugated soluble = yellow eyes and dark urine

post hepatic - conjugated - yellow eyes, pale stool and dark urine

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3
Q

describe the simplified production pathways of bilirubin

A

produced by RBC breakdown = unconjugated
conjugated in the liver and excreted in bile
reabsorbed in the gut for enterohepatic circulation

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4
Q

what liver enzyme tests can be done and what do they show

A

ALT and AST from liver cells = mild increase = chronic disease, sudden rise = acute

leak from bile ducts = all phos - high obstructive jaundice and chronic biliary disease

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5
Q

what investigations can be done for jaundice

A

ultrasound for dilated ducts or liver biopsy

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6
Q

what are the features in he liver of obstructive jaundice

A

bile in the liver parenchyma - yellow skin
oedema, portal tract expansion, ductular reaction
bile salts in the skin = itchy

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7
Q

describe hepatitis

A

inflammation in the liver - non-neoplastic
raised liver enzymes
acute vs chronic

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8
Q

what are the causes and pathology of acute liver disease

A

asymptomatic, malaise, jaundice, coagulophathy
damage to hepatocytes - inflammatory injury, viral, drug, autoimmune alcohol drugs
cell death inflammation and regeneration

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9
Q

what is the most common cause of severe liver cell injury

A

alcohol and paracetamol toxicity

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10
Q

which viral disease cause severe liver damage

A

hep ABE

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11
Q

what are the causes of chronic liver disease

A
virus, autoimmune drugs 
fatty liver disease, alcohol, NAFLD
iron copper genetic error alpha 1 antitrypsin 
biliary disease
vascular disease
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12
Q

what is the pathology of chronic liver disease

A

injury to liver cells - scar tissue and regen - dependant on the cause

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13
Q

describe the progression of chronic liver disease

A

scaring forms bridges with vascular structures = nodule development and cirrhosis

remodelling = bands of fibrosis bridge between portal tracts and hepatic veins

portal blood entering th e liver can flow through vessels in fibrous tissue and not percolate through sinusoids

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14
Q

describe how different viruses affect the liver

A

ABC
D only with B
E waterborne associated with zoonosis
EBV CMV HSV usually in immuncompromised

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15
Q

how does alcohol affect the liver

A

spectrum of fatty change with inflammation = steatohepatitis - cirrhosis
liver biopsy = collagen stained red (van geison stain) - collagen surrounds cells like chicken wire and portal tract fibrosis

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16
Q

describe what NAFLD is in the liver

A

non-alcoholic fatty liver disease

associated with metabolic syndrome such as obesity T2DM, hyperlipidaemia

17
Q

what is the most common cause of liver disease

A

disease associated with NAFLD

18
Q

how does NAFLD change the liver

A

insulin resistance
obesity - long term fat storage in liver = steatohepatitis - fibrosis and inflammation, oxidative stress
slow evolution into cirrhosis

19
Q

what is DILI and how is it classified

A

drug induced liver injury
intrinsic - paracetamol and predictable
idiosyncratic - rare unpredictable (metabolic and immune)

20
Q

what is the most common symptom of DILI

21
Q

what is the most common cause of acute liver failure

A

paracetamol toxicity

22
Q

what are three types of inherited liver disease

A

haemochromatosis
wilsons
alpha 1 antitrypsin deficiency

23
Q

describe haemochromatosis

A

failure of iron absorption regulation - high serum levels of transferrin (HFE C282Y mutation)
high iron = liver cell damage = cirrhosis and carcinoma
t = frequent venesection - remove iron

24
Q

what is the test for haemochromoatosis

A

perls stain = blue for iron

25
what does iron accumulation cause in different organs
``` liver - cirrhosis pancreas - diabetes skin - pigment joint - arthritis heart - cardiomyopathy ```
26
describe inherited wilsons disease
copper metab little caeruloplasmin copper accumulates in eyes, liver brain high urinary copper low serum copper and high in liver tissue
27
what are copper accumulation in the eye called
Keyser Fleischer rings
28
what is the treatment of Wilson disease
chelate copper
29
describe alpha 1 antitrypsin deficiency
normally it neutralises proteolytic enzymes from active state abnormal A1AT - forms globules of glycoprotein - damage liver cells = fibrosis and cirrhosis
30
how can you test for alpha 1 antitryspin deificney
posiitve with PAS diastase stain
31
what do low levels of A1AT lead to
emphysema
32
what is the diagnosis of autoimmune hepatitis
common in women and auto-antibodies against hepatocytes raised IgG, ALT can do liver biopsy
33
describe two types of autoimmune liver disease
primary biliary cholangitis - antimitochondrial antibodies, IgM raised ALP - more common in women primary sclerosis cholangitis - more sinister -more common in men high ALP and associated with UC
34
what can be used to treat PBC and PSC
urso-deocycholic acid
35
what is a major risk factor for hepatocelualr carcinoma
cirrhosis
36
what is cirrhosis and pathogenesis
diffuse hepatic process, fibrosis and conversion of oral liver architectures not abnormal nodules portal vein blood bypasses sinusoids so hepatocytes can perform function portal hypertension
37
what are the complications of cirrhosis
``` oedema bruising muscle wasting lack of detoxifying ascites jaundice and itching from bile salts infection risk ```
38
what happens during hepatic failure
acute and chronic (end stage liver disease) | lead to caput medusa, spider naevi, ascites and muscle wasting