4- pathology of liver Flashcards

1
Q

can liver regenerate?

A

yes, as long as no structural problems

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2
Q

what is cirrhosis appearance macroscopically?

A

bands of fibrosis separating regenerative nodules of hepatocytes
= alteration of hepatic microvasculature (the zones etc)

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3
Q

what are complications of cirrhosis?

A
  • portal hypertension = leads to oesophageal varices, caput medusa (veins from umbilicus), haemorrhoids
  • ascites
  • liver failure
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4
Q

what is pathophysioloogy of alcoholic liver disease?

A

depends on extent of alcohol abuse & individual factors
= ethanol metabolised in liver, the breakdown products of this are toxic→chronic consumption = ROS release →damage of cellular structures →inflammation→activates hepatic stellate →promote fibrosis

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5
Q

what is length of progression of normal liver to cirrhosis in alcohol?

A

fatty liver (2-3 days) →hepatitis (4-6 weeks)→fibrosis (months →years) →cirrhosis

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6
Q

what histological appearance of fatty liver in alcoholic hepatitis?

A

fat vacuoles on fatty liver

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7
Q

what are histological appearances on alcoholic hepatitis when drinking weeks to months?

A
  • hepatocyte necrosis
  • neutrophils
  • mallory bodies (bright pink areas on hepatocytes)
  • pericellular fibrosis
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8
Q

what is histological appearance of alcoholic hepatitis when months to years?

A

collagen (blue) laid around cells

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9
Q

what is NAFLD?

A

non alcoholic fatty liver disease = pathologically identical to alcohol related but more with people for diabetes, obesity, hyperlipidemia

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10
Q

what are obesity related liver diseases?

A
  • NAFLD (non alcoholic fatty liver disease)
  • NASH (non alcoholic steatohepatitis)
  • metabolic syndrome
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11
Q

what hepatitis infection spreads blood borne?

A

hep B&C
= dense portal chronic inflammation

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12
Q

what hepatitis infection spreads faecal oral? and histological appearance

A

hep A&E
= individual necrotic cells

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13
Q

what are the 3 main autoimmune diseases that affect the liver?

A
  • primary biliary cholangitis (PBC)
  • autoimmune hepatitis
  • primary sclerosing cholangitis
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14
Q

what is primary biliary cholangitis?

A

rare autoimmune disease, unknown aetiology
- associated with autoantibodies to mitochondria
= INFLAMED BILE DUCTS - granuloma around it

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15
Q

what is autoimmune hepatitis?

A

autoimmune disease with chronic hepatitis pattern, some triggers like drugs

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16
Q

what is histology of autoimmune hepatitis?

A
  • numerous plasma cells im portal tracts = they infiltrate and cause collapse
  • autoantibodies to smooth muscle
17
Q

what is primary sclerosing cholangitis?

A

= chronic inflammatory process affecting intra & extra hepatic bile ducts which leads to periductal fibrosis, duct destruction jaundice & fibrosis
- associated with ulcerative colitis

18
Q

what is chronic drug induced hepatitis?

A

similar to other hepatitis but may trigger autoimmune hepatitis

= loads of different drugs can affect the liver

19
Q

what are examples of liver storage diseases?

A
  • haemochromatosis
  • wilson’s disease
  • alpha 1 antitrypsin deficiency
20
Q

what is
a) primary haemochromatosis?
b) secondary haemochromatosis?

A

a) genetic condition, increased absorption of iron
b) iron overload from diet, transfusion, iron therapy

21
Q

what is pathophysiology of primary haemochromatosis?

A
  • inherited autosomal recessive condition = gene defect
  • excess iron absorption of iron from intestine, abnormal iron metabolism
  • iron deposited in liver and eventually deposited in portal connective tissue and stimulates fibrosis
22
Q

what can result from primary haemochromatosis?

A

cirrhosis, carcinoma, diabetes, cardiac failure, impotence

23
Q

what is histology of primary haemochromatosis?

A

A brown rusty pigment is visible in liver cells (hemosiderin)

24
Q

what is wilson’s disease?

A
  • Inherited autosomal recessive disorder of copper metabolism
  • Copper accumulates in liver and brain (basal ganglia)
25
what are kayser fleischer rings?
rings from wilson's disease at corneal limbus
26
what biochemical test can help diagnose wilsons disease?
low serum caeruloplasmin
27
what does wilson's disease cause?
chronic hepatitis and neurological deterioration
28
what is alpha 1 antitrypsin deficiency?
Inherited autosomal recessive disorder of production of an enzyme inhibitor = Cytoplasmic globules of unsecreted globules of protein in liver cells
29
what does alpha 1 antitrypsin deficiency?
Causes emphysema and cirrhosis
30
what are primary tumours of liver?
- Hepatocellular adenoma - Hepatocellular carcinoma (Hepatoma)
31
what is hepatocellular adenoma?
- benign but can become large and rupture or bleed - most remain asymptomatic - common in females because associated with oestrogen
32
what is hepatocellular carcinoma?
- associated with cirrhosis due to any cause - usually presents as a mass, pain, obstruction
33
what are 2 patterns to look for when looking down microscope?
1. hepatocytic = cancer of liver cells 2. cholangiocarcinoma = bile duct cancer
34
what metastatic carcinoma?
= This is the commonest explanation for liver tumours especially if multiple. The primary lesion can be almost anywhere within the body - usually incurable but if small then sometimes curable