Biliary and liver disease Flashcards

1
Q

How does conjugated bilirubin appear as in urine?

A
  • Urobilinogen.
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2
Q

What are the key features of the following Viral Hepatitises.

  • A
  • B
  • C
  • D
  • E
A

A: oro-anal sex, fleco-oral, acute, asymptomatic (usually)
B: Serology, most adults are able to clear, never have acute hepatitis. Children stay as carriers.
C: Blood spread (IVDU), chronic infection, patients unaware of infection -> fibrosis, cirrhosis, carcinoma.
D: Superinfection of B
E: Expectant mothers beware, particular morbidity in pregnant women. Faeco-oral, self limiting,

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3
Q

What investigation differentiates HBV from other viral causes.

What do the following Hep B serology markers mean?

  • HbsAg
  • HbeAg
  • Anti-Hbs
  • Anti-Hbc
A
  • All other viral hepatitides can cause acute hepatitis with transaminitis. Most adults clear Hep B and become chronic carriers of Hep C.
  • s: Current infection (acute or chronic)
  • e: Infective
  • Anti-s: Immune
  • Anti-c: caught in past, natural immunity.
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4
Q

What are 3 causes of transaminitis in the 1000s?
What does raised GGT and ALP indicate?
What does low albumin show?
What does 2:1 ratio of AST:ALT indicate?

Give 3 causes of low urea.
Give 2 causes of raised urea.

A
  • Paracetamol, Ischaemic hit, viral.
  • Cholestasis/ obstruction, biliary damage. GGT related to alcohol.
  • Low albumin: poor synthetic liver function
  • AST double ALT means alcoholic hepatitis.
  • Low urea: severe liver damage, malnutrition, pregnancy.
    1. Upper GI bleed/ large protein meal
    2. Dehydration/ AKI- urea excreted renally.
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5
Q

What two conditions come under Non-Alcohol steatohepatitis?

What is the aetiology of NASH.

A
  • Steatosis and steatohepatitis.
    Initial fatty liver due to alcohol abuse. If fat persists (in absence of alcohol), causes inflammation and fibrosis aka steatohepatitis.
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6
Q

NASH is usually found as incidental finding. Give 4 occasional symptoms.

A
  • RUQ pain
  • Fatigue
  • Unexplained weight loss
  • Weakness.

20% of people with NASH will develop cirrhosis.

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7
Q

Give 2 serum LFTs for alcoholic hepatitis.

Chronic liver disease may be expected, what size liver would be found.

A
  • AST:ALT > 2:1
  • Raised GGT.
  • Small liver in chronic liver disease.
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8
Q

What is inheritance of Wilson’s disease?
Where do copper transporters remain intact?
Give 3 locations of copper deposits

A
  • Autosomal recessive, mutation in ATP7B gene.
  • Intact transporters in CNS
    Copper deposition
  • Liver: chronic liver disease
  • Basal ganglia: neuropsychiatric and parkinsonism Sx.
  • Cornea: Keyser Fleischer rings.
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9
Q

Give 3 investigation findings for Wilson’s disease.

A
  • Low serum caereuloplasmin- serum copper carrying protein
  • High urinary copper
  • Low serum Cu- paradoxical (not reliable)
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10
Q

What causes raised iron in haemochromatosis?

  • What is the inheritance pattern?
  • Give 3 locations of iron deposition.
  • Give 4 presenting features of haemochromatosis
A
  • Increased dietary absorption and increased release from macrophages.
  • Autosomal recessive
  • Liver, pancreas, pituitary gland
  • Bronzed skin
  • MCP arthritis
  • Diabetes
  • hepatomegaly
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11
Q

What will the following haematinic levels be in haemochromatosis?

  • Ferritin
  • Transferin
  • TIBC

What protein is mutated in 90% of cases?

A
  • Ferritin high- lots of storage
  • Transferrin low
  • TIBC low
  • Hepcidin: deficiency means hepcidin cannot inhibit ferroportin. Increased intestinal absorption of Fe means high serum iron.
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12
Q

Which antibody is present in autoimmune hepatitis?

What type of patient is suspect?

A
  • Anti-smooth muscle antibodies.

- Young female, overweight, autoimmune conditions.

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13
Q

Differentiate biliary colic, acute cholecystitis and cholangitis by Charcot’s triad.

What are 5 Fs of gallbladder disease?
What is order of investigations for gallbladder disease?

A

Biliary colic: RUQ pain
Acute cholecystitis: RUQ pain + Fever. Murphy’s sign +ve
Cholangitis: RUQ + Fever + jaundice

Fat, Female, 40, Fertile, FHx

  1. LFTs
  2. Abdo USS- gold standard Dx
  3. Then consider MRCP
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14
Q

What is management of cholelithiasis?

What is management of choledocholithiasis?

A

Cholelithiasis: Cholecystectomy
Choledocholithiasis: ERCP.

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15
Q

What are the 2 investigations for pancreatic cancer.
What type are most pancreatic cancers?
How may it also present?

What is Courvoisier law?

A
  • LFTs, Protocol CT scan
  • 90% are adenocarcinoma
  • May present as sudden onset diabetes mellitus.
  • Courvoisier law: palpable gall bladder in presence of painless jaundice is unlikely to be due to stones.
    i. e. palpable GB + Jaundice = head of pancreas/ CBD cancer.
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16
Q

Give 3 aetiologies of hepatocellular carcinoma.
What is relevance of cereals?
What investigation should be considered for liver cancer?
Which tumour marker is relevant in liver cancer?

A
  • Chronic hepatitis, metabolic disease (Wilson’s, haemochromatosis), alpha-1 antitrypsin deficiency.
  • Fungal constipation of cereals contain aflatoxins
  • Consider urgent direct access ultrasound scan
  • Alpa-fetoprotein
17
Q

What two conditions are related to cholangiocarcinoma?

What is the marker of pancreatic cancer and cholangiocarcinoma?

A
  • Ulcerative colitis + primary sclerosing cholangitis.

- Ca19-9

18
Q

Give 4 features of a simple liver cyst.

A
  • Lined with biliary-type epithelium but cyst fluid doesn’t contain bile
  • RUQ pain
  • Female >men
  • Found incidentally
19
Q

Describe an infectious liver cyst.

Give 3 pathogenic aetiologies of infectious liver cyst.

A
  • Mass filled with pus in liver
  • Pyogenic = polymicrobial (80%)
  • Amoebic = entamoeba histolytica (10%)
  • Fungal = candida (10%).
20
Q

Describe Primary Biliary Cholangitis by:

  • Pathology
  • Typical patient
  • Investigations
  • Associations
A

Biliary: chronic inflammation

  • Path: intrahepatic bile duct granulomatous destruction by antibodies.
  • Patient: Itchy females, fatigue, dry eyes and mouth.
  • Ix: Anti-mitochondrial M2 antibodies
  • Assoc.: Hypercholesterolaemia: tendon xanthoma, xanthelasma
21
Q

Describe Primary Sclerosing Cholangitis by:

  • Pathology
  • Typical patient
  • Investigations
  • Associations
  • Cancer
A

Sclerosing: chronic cholestatic liver disease.

  • Path: intra and extra hepatic bile duct destruction. Biliary obstruction. Back pressure to liver causes sclerosis.
  • Patient: People with IBD, UC. 40s-50s.
  • Ix: MRCP beads on string
  • Assoc: UC, cholangiocarcinoma
  • Cancer: Bile duct, colonic cancer.