approach to jaundice Flashcards
● Complete absence
of glucuronyl transferase
● Liver transplant
● Rare
type I crigler-najjar syndrome
● Decreased activity
of glucuronyl transferase
● Phenobarbital
● More common
type II crigler najjar
impaired conjugation/clearance of bilirubin
gilbert’s syndrome
mutation in the promoter/coding region of UDPGT gene
gilberts syndrome
Defect in the secretion of bilirubin glucuronides
into the bile canaliculus, chronic conjugated
dubin-johnson
biopsy dubin johnson
dark brown, iron free, granules in liver and kupfer cells
defect in intracellular binding of organic ions
rotor syndrome
deficiency in major hepatic drug uptake transporters: OATP1B1 and OATP1B3
rotor
Environmental toxin
(Vinyl Chloride, Jamaica
Bush Tea, Kava Kava, Wild Mushroom)
(autoimmune,
predominantly middle-aged women – progressive
destruction of interlobar bile duct)
primary biliary cirrhosis
(destruction
and fibrosis of larger bile duct)
primary sclerosing cholangitis
may reflect rhabdomyolysis or
injury to organs (heart, skeletal muscle, kidneys,
pancreas)
Elevated AST
Alcohol-related liver disease = AST to ALT
> 2
> 500 IU/L; normal, < 40 IU/L
acute hepatocellular necrosis or injury, usually result from any of the following:
○ Acute viral hepatitis
○ Toxin – or drug- induced hepatitis
○ Ischemic hepatitis or hepatic infarction
Modest elevations (300 to 500 IU/L)
cheinic liver disorders