GI And liver Flashcards

(45 cards)

1
Q

DNA hepatitis

A

B

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2
Q

Unenveloped hepatitis

A

A and E

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3
Q

IV hepatitis

A

BCD

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4
Q

Hep A diagnosis

A

Serum IgM ABs

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5
Q

Hep B diagnosis

A

HBsAg
AB to HBcAg
PCR for HBV DNA

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6
Q

Hep C diagnosis

A

3rd gen ELISA for AB detection
PCR for HCV RNA

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7
Q

Hep D Diagnosis

A

IgM and IgG ABs
Serum RNA
HDAg in liver

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8
Q

Hep E diagnosis

A

IgG and IgM ABs serum
PCR for RNA

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9
Q

Serology carrier hep B

A

HBsAg present
HBeAg not present
Anti HBeAB present
Normal transaminases
Low/ undetectable HBV DNA
Liver bx no inflamation or necrosis

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10
Q

UC

A

spreads prox from rectum
broad based shallow ulcers, mucosa only
no strictures
multiple pseudopolyps
toxic megacolon

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11
Q

Crohns

A

skip lesions
cobblestone
transmural
rik calcium oxalate stones
strictures, deep ulcers
non caseating granulomas

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12
Q

coeliac

A

tissue transglutaminase and gliadin blood tests
diffuse enteritis with flattened villi
assoc dermatitis herpetiform

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13
Q

Whipple disease

A

assoc HLA B27
tropherma whippeli infection
lamina propria SI laden macrophages
diarrhoea, statorrhoea, fever weight loss, migratory arthritis, brain involvement

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14
Q

Blood tests liver

A

hepatocyte - ALT AST LDH
bile canaliculi - ALP GGT

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15
Q

Scar formation liver

A

collagen release by stellate (Ida cells)

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16
Q

Cirrhosis morphology

A

proliferating hepatocyte surrounded by on going fibrosis
- fibrous septae
- parenchymal nodules
- disruption architecture

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17
Q

Acute liver failue

A

80% function lost
80% die without transplant

acute illness assoc encephalopathy and coagulopathy
within 26 weeks initial illness
absence pre existing liver disease

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18
Q

Ascites

A

85% due to cirrhosis
low protein fluid
amount of lymph thoracic cavity exceeds thoracic duct capacity

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19
Q

Mortality acute on chronic hepatic failure

20
Q

HBV % acute and chronic

A

65% subclinical
25% acute
10% chronic

21
Q

HCV % chronic

A

80%, main cause IVDU

22
Q

HIV % with hepatitis

A

10% HBV
25% HCV

23
Q

Chronic hepatitis morphology

A

mononuclear portal infiltration
hepB ground glass hepatocytes
hepC lymphoid aggregates and bile duct injury

24
Q

Type 1 autoimmune hepatitis

A

middle aged/ old
ANA and anti smooth muscle actin ABs

plasma cells as infiltrate

25
Type 2 autoimmune hepatitis
kids/ teenagers anti liver kidney microsome 1 antibodies plasma cells as infiltrate
26
Hepatic cancer associations
hepatocellular adenoma - OCC and anabolic steroids HCC - ETOH angiosarcoma - vinyl chloride
27
Stages alcoholic liver disease
1. steatosis (reversible) fatty change and perivenular fibrosis 2. hepatitis (reversible) hepatocyte swelling, mallory bodies, neutropilic infiltrate 3. fibrosis and cirrhosis (non reversible) extensive fibrsosis with hyperplastic nodules
28
NAFLD
>5% hepatocytes invlved less mallory bodies and more mononuclear cells tan ETOH 80% isolated fatty liver, 20% NASH which is progressive
29
Unconjugated bilirubin
insoluble in water highly albumin bound unbound crosses BBB and icteric sclera increased unbound in haaemolytic disease or when drugs displace
30
Causes unconjugated bilirubinaemia
neonatal jaundice criggler najar gillbert syndrome
31
Biliary atresia
conjugated fetal/ perinatal (more common) obstruction biliary tree viral/ autoimmune hepatic or common bile duct
32
Primary biliary cirrhosis
autoimmune cholangiopathy destruction small medium bile ducts female in 50s assoc sjorgens 95% AMA dx bx
33
Primary sclering cholangitis
autoimmune cholangiopathy intra and extrahepatic bile ducts with dilation and preserved segments male 30s assoc IBD 65% ANCA radiology strictures and beading large bile ducts
34
Gallstone types
cholesterol - most common, radiolucent unless contain calcium carbonate pigment - insoluble calcium salts and unconjugated bilirubin brown infected and radiolucent black sterile and radioopaque
35
Morphology chronic cholecystitis
suserosal fibrosis outpouchings epithelium porxelein gallbladder hydrops gallbladder end stage
36
Cirrhosis collagen
TI and III normally in portal tracts and around veins - deosited in lobules, neovascularisation TIV in space of disse
37
Pathogenesis acute pancreatitis
pancreatic duct obstruction primary acinar cell injury defective intrracellular release proenzymes
38
Main cause acute panreatitis
80% alcohol and gallstones
39
Hereditory pancreatitis
assoc 25% of pacreatitis 40% risk cancer CFTR SPINK1
40
Blood tests pancreatitis (timing)
amylase in 24h lipase in 72-96h decreased Ca2+ 10% glycosuria
41
Cause and mortality chronic pancreatitis
Mainly alcohol TGFbeta and PDGF fibrogenic factors 25y mortality 50%
42
Autoimmune pancreatitis
IgG4 secreting plasma cells in pancreas responsive to steroid therapy similar symptoms to cancer
43
Chronic hepatitis
Symptoms/biochemical/serological evidence for > 6m
44
Hepatitis carrier
Harbours and can transmit No symptoms
45
Virus causing ischaemic gut
CMV