GI 2 Flashcards

1
Q

Most common causes of cirrhosis?

A

In W. world = alcohol

Worldwide = Hep B & C

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2
Q

What are the two main types of cirrhosis?

A

Micronodular - uniform small nodules, often following alcoholic hepatits
Macronodular - variable size nodules, usually after chronic viral hepatitis

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3
Q

What features would indicate DECOMPENSATED cirrhosis?

A
  • hepatic encephalopathy
  • ascites
  • variceal haemorrhage (–> haematemesis)
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4
Q

General clinical features of cirrhosis (seen in compensated and decompensated)?

A

jaundice
fever
loss of body hair

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5
Q

What is fetor hepaticus

A

Distinctive musty sweet breath odour found in decompensated cirrhosis.

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6
Q

When would you see Serum alpha fetoprotein (AFP) ?

A

usually only high in fetus but can increase with chronic liver disease and if >200ng/mol = strongly suggestive of HCC!

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7
Q

How would you assess severity and prognosis in Cirrhosis?

A
CHILD-PUGH classification - 5 factors
- encephalopathy
- ascites
- prothrombin time
- serum bilirubin
- serum albumin
Or MELD score = serum bilirubin, creatinine and INR
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8
Q

What is PBC?

A

= primary biliary cirrhosis –> chronic disorder with progressive destruction of intrahepatic bile ducts causing cholestasis and eventually cirrhosis.

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9
Q

what is the only specific Ab in PBC?

A

M2 Ab ( an AMA) = anti-mitochondrial antibody

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10
Q

If pt has high serum ALP, high IgG and a positive AMA Ab test, what is the most likely diagnosis?

A

Primary biliary cirrhosis

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11
Q

Mx of PBC?

A

lifelong ursodeoxycholic acid = a naturally occurring bile acid (slows progression)
then supplements for malabsorption and transplant after disease progression.

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12
Q

Cardinal sign of alcoholic hepatitis?

A

rapid onset jaundice

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13
Q

What is characteristic histological appearance of alcoholic hepatitis?

A

steatosis with ballooned hepatocytes, often containing amorphic eosinophilic material called MALLORY BODIES

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14
Q

What would liver biochem show in alcoholic hepatitis

A

rise in AST & ALT with DISPROPORTIONATE RISE IN AST
marked increase in serum bilirubin
low albumin
prolong prothrombin time

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15
Q

A bile duct bx shows bile duct carcinomas, what condition would this likely indicate?

A

PBC (autoimmune attack of bile ducts)

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16
Q

Clinical presentation of Haemochromatosis?

A

classic triad of: micronocular cirrhosis, DM, and skin pigmentation
others = signs of iron loading in organs

17
Q

Mx of haemochromatosis?

A

Venesection
chelation with deferoxamine
(surveillance for HCC development and genotyping of 1st degree relatives)

18
Q

What is caeruloplasmin?

A

= main copper carrying protein in the blood

19
Q

Where does copper accumulate in Wilsons disease?

A

cornea, basal ganglia, liver, kidney, joints

20
Q

signs of liver failure? (5)

A
jaundice
hepatic encephalopathy
asterixis (flap)
fetor hepaticus
constructional apraxia
(+ signs of chronic liver disease)
21
Q

What is Budd Chiari syndrome?

A

= thrombosis of the portal vein

Caused by: pregnancy, polycythemia vera and OCP

22
Q

Signs of ascites?

A
jaundice/other liver disease symps
abdo distension
puddle sign
shifting dullness
fullness in flanks
fluid thrill
pleural effusion and oedema maybe
23
Q

How do intestinal tumours present?

A

Abdo pain, anorexia, anaemia and diarrhoea.

24
Q

in what condition do you see a 100% lifetime risk of CRC?

A

Familial adenomatous polyposis.

25
Q

Give some examples of hepatotoxic drugs

A
paracetamol, 
MTX, 
isoniazid, 
azathioprine, 
oestrogen, 
tetracycline