LIVER Flashcards

(42 cards)

1
Q

What are the 3 commonest causes of HEPATOMEGALY?

A
  • Cirrhosis
  • Malignancy
  • RHF
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2
Q

What are the palpation findings of hepatomegaly caused by liver cirrhosis?

A
  • initially enlarged then decreases in size as cirrhosis progresses
  • non tender firm liver
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3
Q

What are the palpation findings of hepatomegaly caused by malignancy?

A

Hard irregular liver edge

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4
Q

What are the palpation findings of hepatomegaly caused by right heart failure?

A

Firm, smooth, tender liver edge

May be pulsatile

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5
Q

3 branches of the coeliac trunk?

A
  • left gastric artery
  • splenic artery
  • common hepatic
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6
Q

2 branches of the common hepatic artery

A

proper hepatic

& gastro duodenal artery

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7
Q

what artery supplies the liver

A

hepatic artery proper

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8
Q

what 2 veins drain into the hepatic portal vein

A
  • splenic vein

- superior mesenteric vein

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9
Q

what is the portal triad

A
  • hepatic artery
  • portal vein
  • common bile duct
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10
Q

list the liver function tests

A
  • Liver enzymes: ALT & AST
  • ALP
  • GGT
  • Bilirubin
  • Albumin
  • PT/INR
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11
Q

cause of low albumin & high protein

A

multiple myeloma

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12
Q

cause of low albumin & normal protein

A

infection

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13
Q

when is jaundice usually detected

A

when serous bilirubin is above 50 umol/L

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14
Q

what is Haem in RBC broken down into

A

Biliverdin and then bilirubin

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15
Q

where does conjugation of bilirubin occur?

A

liver, hepatocytes

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16
Q

where does urobilinogen go?

A
  • oxidised by bacteria in intestine to stercobilin which gives stool its pigmentation
  • transported by the blood to the kidney converted to urobilin giving urine its characteristic colour
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17
Q

what type of jaundice goes haemolysis cause?

A

pre hepatic jaundice; high levels of serum bilirubin

18
Q

5 causes of haemolysis?

A

1) mechanical - metallic valve prostheses
2) Autoimmune haemolytic anaemia
3) Malaria infection
4) Transfusion reactions
5) Congenital red cell problems - sickle cell anaemia/hereditary spherocytosis

19
Q

what does high levels of conjugated hyperbilirubin mean?

A

there is an obstruction to the outflow tract of bile

20
Q

causes of post hepatic jaundice?

A
  • pancreatic cancer
  • gall stones
  • pancreatitis
21
Q

ALT > AST indicates?

A

hepatocyte damage - chronic liver disease

22
Q

what could low albumin & protein indicate (3)

A
  • decreased intake: malnutrition
  • decreased synthesis: cirrhosis, alcoholism, chronic inflammation
  • increased excretion: nephrotic syndrome
23
Q

AST:ALT < 0.8

A

indicates that ALT is greater than AST therefore non- alcoholic liver disease

24
Q

bone pathologies that cause raised ALP

A
  • ostomalacia
  • Pagets disease
  • fractures
  • multiple myeloma
25
define chronic hepatitis
sustained inflammation of the liver lasting longer than 6 months
26
hereditary causes of chronic hepatitis
- Wilsons disease | - Haemochromatosis
27
excess accumulation of copper in body and tissues?
wilsons disease
28
what is mutation and chromosome location in wilsons disease?
ATP7B copper binding protein, located on chromosome 13
29
inheritance of wilsons disease?
autosomal recessive
30
neurological manifestations of Wilsons disease? (4)
- concentration - coordination - dysarthria - dystonia
31
psychiatric mainfestations of wilsons disease? (2)
- mild depression | - psychosis
32
name and appearance of copper deposition in the eyes in wilsons disease?
brown rings in descends corneal membrane kayser-fleischer rings
33
screening blood test for Wilsons disease?
Serum caeruloplasmin (protein that carries copper)
34
definitive gold standard test for Wilsons disease?
liver biopsy
35
management of Wilsons disease?
Copper chelation medications - penicillamine - trientene
36
Iron storage disorder where there is excessive total body iron & high iron deposition in tissues
Haemochromatosis
37
haemochromatosis gene mutation? & inheritance?
Human haemochromatosis protein located on chromosome 6 autosomal recessive inheritance
38
what does iron deposits in the skin cause in haemochromatosis
bronze tinge to skin
39
management of haemochromatosis
weekly venesection monitor serum ferritin
40
what are the 2 main organs affected by alpha-1-antitrypsin deficiency & how?
Lungs - bronchiectasis * emphysema due to excess protease enzymes attacking connective tissue in lungs Liver - Liver cirrhosis, which can progress to hepatocellular carcinoma
41
what does alpha 1 antitrypsin deficiency cause?
the protein offers protection by inhibiting the neutrophil elastase enzyme which is an enzyme that digests connective tissues
42
marker for hepatocellular carcinoma
AFP alpha-fetoprotein