liver disease Flashcards

1
Q

causes of jaundice

A

medical doctors aren’t very happy
surgeons aren’t much better

Malignancy
Drugs
Antibiotics 
Viruses
Haematological
Stones 
Alcohol
Malignancy of pancreatic head
better
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2
Q

acute liver disease classified as ?

A

less than 6 months

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3
Q

what is acute liver disease/

A

the rapid development of hepatic dysfunction without prior liver disease causing encephalopathy and prolonged coagulation

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4
Q

investigations for liver disease?

A

LFTs, prothrombin time, history and examination , ultrasound, virology, rarely liver biopsy

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5
Q

tereatment of liver disease?

A

rest
NO ALCOHOL
increase calories

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6
Q

which kind of foods are poorly tolerated in liver disease?

A

high fat foods

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7
Q

what can you do for itch symptoms ?

A

sodium bicarbonate bath
cholestyramine
orseodeoxycholic acid

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8
Q

how long would hepatic drug reactions take?

A

6 weeks from exposure to effect

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9
Q

what is the definition of fulminant hepatic failure?

A

jaundice and encephalopathy in a patient with a previously normal liver

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10
Q

what is wilsons disease?

A

build up of copper in the body

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11
Q

what sign do you get in the eyes in wilsons?

A

kaiser Fleischer rings

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12
Q

causes of fulminant hepatic failure?

A

paracetamol, viral, drugs,

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13
Q

treatment of FHF?

A

inotropes and fluid, renal replacement, management of raised ICP

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14
Q

chronic liver failure time frame?

A

> 6months

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15
Q

what are the stages leading to cirrhosis

A

Inflamation –> fibrosis –> cirrhosis

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16
Q

PBC - what antibodies associated with it?

A

IgM and AMA

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17
Q

who typically gets PBC?

A

women, middle aged presenting with itch

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18
Q

In PBC, what would you expect to be up ?

A

GGT and ALP (bile)

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19
Q

In late disease in PBC, what would happen to bilirubin, prothrombin time and albumin?

A

bilirubin up, PT up, albumin down

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20
Q

in liver disease, when does albumin drop?

A

late

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21
Q

tx of PBC?

A

urseodeoxycholic acid and transplant

can give cholestyramine for itch

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22
Q

on histology, what would you see in PBC?

A

granulomas and bile duct loss (mum gran)

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23
Q

what would bile ducts look like in PBC?

A

chronic portal inflammation, bile ducts inflamed

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24
Q

ultimately, what could PBC progress to

A

cholestasis liver injury, inflammation, fibrosis and cirrhosis

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25
who gets autoimmune hepatitis more? women or men?
women
26
what would you expect on examination in AIH?
hepatomegaly, splenpmegaly, jaundice
27
AIH - what markers are up? (AIG)
AST, ALT, IgG
28
Interface hepatitis, with marked piecemeal necrosis and lobular involvement, plasma cells?
autoimmune hepatitis
29
hw may yes of autoimmune hepatitis are there?
3
30
which one would be more common in children and young adults?
2
31
primary sclerosing cholangitis, big association with?
UC
32
what do you get destruction of in PSC?
destruction of large/medium sized bile ducts
33
how do you describe the appearance of fibrosis of bile ducts in PSC?
periductal ONION SKINNING fibrosis, jaundice, and fibrosis
34
male or female patients more likely to get PSC?
male
35
which kind of carcinoma is heavily associated with PSC(15%)
cholangiocarcinoma
36
antibodies in PSC?
AMA -ve, ANA, SMA, ANCA may be positive
37
sexual dysfunction in haemachromatosis?
men can't get erection
38
where is iron deposited in the liver?
portal connective tissue --> this stimulates fibrosis
39
haemochromotosis - how long can it take to develop?
years - iron is deposited in the liver for years
40
in haemochromotosis, what would you do in terms of the heart?
an ECG/echo - iron can be deposited in heart
41
what is the treatment of haemochromotosis ?
venesection - continual removal of blood
42
wilsons - what is the mode of inheritance?
autosomal recessive, same as haemochromotosis
43
what is the copper binding protein called in which you get a loss of function in wilsons ?
caeruloplasmin
44
where does copper accumulate in the body?
liver and the brain (basal ganglia)
45
what kind of movements do you get in wilsons and what can it do to personality ?
chorea-athetoid movements | depression, mania, labile emotions, changed libido, personality change
46
what would you see in eyes in wilsons?
kaiser Fleischer rings
47
treatment of wilsons?
copper chelating drugs
48
alpha 1 anti trypsin deficiency. as well as emphysema, what can this cause in liver?
liver damage through deposition of A1A
49
what is budd chiari?
thrombosis of hepatic veins
50
presentation of bud chiari?
jandice and ascites
51
diagnosis of bud chiari?
hepatic vein ultrasound
52
how could the heart cause cirrhosis?
secondary to high right heart pressure
53
- Final, irreversible common endpoint for liver disease
cirrhosis
54
micronodular and macronodular cirrhosis. which one is alcoholic ?
micronodular mick
55
complications of cirrhosis
portal hypertension, oesophageal varices, caput medusa, haemarrhoids
56
what is encephalopathy?
brain damage, disease or malfunction
57
why do you get encephalopathy in liver disease?
a build up of ammonia (liver removes ammonia from your body)
58
classification to predict liver dysfunction /
child pugh (grade A -> C(most severe)
59
causes of portal hypertension?
``` pre hepatic (portal vein thrombosis or occlusion) intrahepatic - presinusoidal (schistisomiasis) post sinusoidal (cirrhosis, alcoholic hepatitis, congeital fibrosis) post hepatic - bile problems ```
60
intrahepatic causes of portal hypertension (pre and post sinusoidal)
pre sinusoidal - schistisomiasis and non cirrhotic portal hypertension post sinusoidal - cirrhosis
61
what is SBP?
spontaneous bacterial peritonitis
62
what is SBP?
translocated bacterial infection of ascites
63
what should you do in all ascites to investigate?
tap - neutrophil count (>250)
64
treatment of ascites?
antibiotics and alba, terlipressin
65
prevention of variceal bleeding?
BBlockers (propranolol and ligation)
66
causes of jaundice ?
medical doctors aren't very happy surgeons are not much better ``` malignancy drugs alcohol viral haematological stones antibiotics malignancy of pancreatic head ```
67
how would you identify biliary problems ?
us scan
68
what is the treatment for hepatitis?
acute - supportive | chronic - interpheron alpha or antiviral/tenofovir etc)
69
haematological what do you get in all infectious individuals in hep B?
HBsAG
70
how is hep C spread?
by blood
71
what is the progression of Hep C ?
acute and becomes chronic
72
what does the presence of anti hb sag indicate?
clinical recovery and immunity
73
Hep C is only an RNA vaccine, how do you test for it?
by PCR -> there is no vaccine
74
is there a vaccine available for hep B?
yes
75
markers of acute infection and chronic infection in hep B
♣ IgM antiHBc – acute infection | ♣ IgG antiHBc – chronic infection
76
how do you get hepatitis E?
undercooked, contaminated food
77
what is the muscle in the cheek that moves during food mastication?
buccinator
78
why do you need to be careful when using ferritin values for iron?
ferritin is an acute phase protein - may be synthesised in increased quantities during inflammation.
79
how do you measure iron overload?
transferrin saturation (less than 50% in males and 45% in females)
80
when would ferritin levels be decreased?
in iron deficiency anaemia
81
what are both duputryens contracture and parotitis signs of?
alcoholic liver disease