alimentary disease Flashcards

jaundice: recall the features and aetiology of jaundice (pre-hepatic, hepatic, post-hepatic), and the pathogenesis of the symptoms and signs associated with jaundice

1
Q

what is jaundice

A

yellow discolouration of sclerae and skin due to raised bilirubin, and is clinically detectable when serum bilirubin >40umol/litre

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2
Q

3 categories of jaundice

A

haemolytic, jaundice caused by congenital hyperbilirubinamias, cholestatic

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3
Q

what is affected in prehepatic jaundice

A

conversion of Hb to bilirubin

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4
Q

cause of prehepatic jaundice

A

haemolysis

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5
Q

what is affected in intrahepatic cholestatic jaundice

A

conjugation of bilirubin

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6
Q

causes of intrahepatic cholestatic jaundice

A

viral hepatitis, drugs, alcoholic hepatitis, cirrhosis, pregnancy, recurrent idiopathic cholestasis, some congenital disorders, infiltrations

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7
Q

what is affected in extrahepatic cholestatic jaundice

A

failure of bile secretion by liver, or bile duct obstruction

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8
Q

causes of extrahepatic cholestatic jaundice

A

common duct stones, carcinomas in bile duct, head of pancreas and ampulla, biliary structure, sclerosing cholangitis, pancreatitis, pseudocyst

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9
Q

example of haemolytic anaemia

A

sickle cell disease

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10
Q

process of haemolytic jaundice

A

increased erythropoiesis → increased production of bilirubin → jaundice

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11
Q

does bilirubin in haemolytic jaundice pass into urine

A

no as not water soluble as unconjugated

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12
Q

liver biochemistry for haemolytic jaundice

A

increased serum urobilinogen, otherwise normal

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13
Q

cause of jaundice caused by congenital hyperbilirubinaemia

A

impaired conjugation of bilirubin with glucoronic acid, or bilirubin handling by liver

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14
Q

liver biochemistry for jaundice caused by congenital hyperbilirubinaemia

A

raised bilirubin, otherwise normal

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15
Q

what is the commonest cause of congenital hyperbilirubinaemia

A

Gilbert’s syndrome

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16
Q

how does Gilbert’s syndrome lead to congenital hyperbilirubinaemia

A

autosomal dominant; mutation in gene coding for UDP-glucuronyl transferase → reduced enzyme activity → reduced conjugation of bilirubin

17
Q

how is Gilbert’s syndrome picked up

A

incidental finding of slightly raised serum bilirubin as asymptomatic

18
Q

triggers of Gilbert’s syndrome that lead to jaundice

A

dehydration, fasting, viral illness

19
Q

diagnosis of jaundice caused by congenital hyperbilirubinaemia

A

raised unconjugated hyperbilirubin, otherwise normal liver biochemistry, normal full blood count, smear and reticulocyte count (differentiate from haemolysis), absence of signs of liver disease

20
Q

management of jaundice caused by congenital hyperbilirubinaemia

A

reassurance that no further investigation or treatment necessary

21
Q

other causes of jaundice caused by congenital hyperbilirubinaemia

A

Crigler-Najjar, Dubin Johnson, Rotor’s syndromes

22
Q

what causes intrahepatic cholestasis

A

hepatocellular swelling or abnormalities at cellular level of bile excretion

23
Q

what causes extrahepatic cholestasis

A

obstruction of bile flow at any point distal to bile canaliculi

24
Q

characteristics of cholestatic jaundice

A

conjugated bilirubin, pale stool, dark urine, abnormal liver biochemistry