Liver Disease Flashcards

1
Q

What is the definition of cirrhosis of the liver?

A
  • end stage liver disease
  • diffuse process with fibrosis and nodule formation
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2
Q

Describe a typical history of someone with liver disease

A

Symptoms:
- jaundice, dark urine + light stool with itch
- ankle swelling, abdo swelling, RUQ pain
- nausea/ vomiting, fever, GI symptoms

PMH: previous jaundice, cholecystectomy, T2DM, obesity, thyroid disease, other autoimmune disease

DH: new medications, OTC, herbal

SH: drug use, alcohol, sexual partner(s)

FH: jaundice, liver tumours, haemochromatosis

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3
Q

What is raised in hepatic causes of liver disease?

A
  • AST
  • ALT
  • bilirubin
  • GGT
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4
Q

What is raised in cholestatic causes of liver disease?

A
  • ALP
  • bilirubin
  • GGT
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5
Q

What are the best measures of liver function?

A
  • albumin
  • bilirubin
  • prothrombin time
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6
Q

What are the causes of acute liver injury?

A
  • acute viral hepatitis
  • autoimmune liver disease (hepatitis)
  • paracetamol toxicity (‘therapeutic’ doses can be toxic if underweight/alcohol misuse/malnutrition)
  • drug induced
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7
Q

What investigation would you do if you suspected liver disease?

A

Ultrasound

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8
Q

What are the causes of acute cholestasis/cholestatic hepatitis?

A
  • extrahepatic biliary obstruction
  • drug injury
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9
Q

What are the causes of chronic liver disease?

A
  • chronic viral hepatitis (HBV, HCV)
  • autoimmune liver disease (hepatitis, primary biliary cholangitis, primary sclerosing cholangitis)
  • metabolic liver disease (haemochromatosis, wilson’s disease, alpha-1 anti-trypsin deficiency)
  • fatty liver (alcoholic/non-alcoholic)
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10
Q

What are the investigation results for autoimmune hepatitis?

A
  • raised AST and ALT
  • positive ANA, SMA, anti-liver kidney microsomal antibodies
  • raised IgG levels
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11
Q

What is the treatment for autoimmune hepatitis?

A
  • corticosteroids (prednisolone, budesonide)
  • azathioprine, mycophenolate
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12
Q

What are some associations with primary biliary cholangitis?

A
  • Sjorgren’s syndrome
  • systemic sclerosis
  • RA
  • lupus
  • hypothyroidism
  • coeliacs disease
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13
Q

What are the investigation results and treatment for primary biliary cholangitis?

A
  • elevated GGT and ALP (early disease)
  • elevated bilirubin (advanced disease)
  • treatment: ursodeoxycholic acid
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14
Q

Describe Wilson’s disease

A
  • mutation in ATP7B gene resulting in inability to transport excess copper into bile = bile accumulation
  • AR inheritance
  • presents with chronic liver disease with neurological/psychiatric symptoms (eg. Parkinsonism, hand tremor, masked facial expression, slurred speech, ataxia, dystonia)
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15
Q

What are the investigation results and treatment of Wilson’s disease?

A
  • low caeruloplasmin, high copper levels,
  • treatment: copper chelation (panicillamine, trientine) or oral zinc (to reduce copper absorption)
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16
Q

Describe hereditary haemochromatosis

A
  • iron accumulation in tissues and organs including liver, adrenal glands, heart, skin, gonads, joints and pancreas
  • presents with abnormal LFTs and chronic liver disease, polyarthropathy, adrenal insufficiency, HF, or diabetes (+/- pigmentation)
  • due to mutation in HFE gene
  • AR inheritance
17
Q

What are the investigation results for hereditary haemochromatosis?

A
  • raised ferritin and transferrin saturation
  • liver MRI for iron, liver biopsy
  • treatment: venesection
  • family screening (1st degree)