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HYPERBILIRUBINEMI. Prof.Dr.Arzu SEVEN. HYPERBILIRUBINEMI (Bilirubin > 1mg/dl in blood). Types of bilirubin: İndirect bilirubin=free bilirubin=unconjugated bilirubin Free bilirubin en route to liver from RES, where it is produced from the breakdown of heme porphyrins.
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HYPERBILIRUBINEMI Prof.Dr.Arzu SEVEN
HYPERBILIRUBINEMI(Bilirubin>1mg/dl in blood) • Types of bilirubin: • İndirect bilirubin=free bilirubin=unconjugated bilirubin • Free bilirubin en route to liver from RES, where it is produced from the breakdown of heme porphyrins. .
As it is water _insoluble, it requires methanol to be coupled with diazo reagent • Direct bilirubin=conjugated bilirubin=bilirubin glucuronide: • Bilirubin that is ready to be excreted into the bile
As it is water soluble, it can react directly with diazo reagent. Only conjugated bilirubin can occur in the urine .
DELTA bilirubin: • Conjugated bilirubin that is covalently bound to albumin, has a longer half life in plasma than conventional conjugated bilirubin .
It remains high during the recovery phase of obstructive jaundice after the remainder of conjugated bilirubin has decreased to normal level.
Hyperbilirubinemi may be due to: • a)production of more bilirubin than normal liver can excrete:PREHEPATİC • b)failure of damaged liver to excrete normal amounts of bilirubin, impaired hepatic uptake, conjugation or secretion of hepatic bilirubin:INTRAHEPATIC • C)obstruction of the excretory ducts of liver:POST HEPATIC
Depending on the type of bilirubin present in plasma, hyperbilirubinemia may ve classified as: • 1)retention hyperbilirubinemia due to overproduction. • 2)regurgitation hyperbilirubinemia due to reflux into the bloodstream because of biliary obstruction.
Because of its hydrophobicity only unconjugated bilirubin>20-25mg/dl can cross the blood_brain barrier into the central nervous system. • Toxic encephalopathy due to hyperbilirubinemi (KERNİCTERUS) can occur in retention hyperbilrubinemia.
Choluric jaundice occurs in regurgitation hyperbilirubinemia. • Acholuric jaundice occurs only in the presence of excess unconjugated bilirubin. .
Obstruction of the biliary tree is the commonest cause of conjugated hyperbilirubinemia . Blockage of the hepatic or common bile ducts,most often due to a gallstone or pancreas head cancer
Conjugated bilirubin can not be excreted due to obstruction it regurgitates into hepatic veins γ lymphatics it appears in blood γ urine (choluric jaundice)
Cholestatic jaundice: all cases of extrahepatic obstructive jaundice
Dubin Johnson Syndrome • Benign autosomal recessive disorders • Conjugated hyperbilirubinemia in childhood or during adult life • Mutations in the gene encoding MRP-2, the protein involved in the secretion of conjugated bilirubin into bile • Centrilobuler hepatocytes contain abnormal black pigment derived from epinephrine .
Rotor Syndrome • Rare benign condition • Chronic conjugated hyperbilirubinemia • Normal liver histology • Abnormality in hepatic storage
Neonatal physiologic jaundice • Accelerated hemolysis around the time of birth • Immature hepatic system for the uptake,conjugated and secretion of bilirubin • enzyme activity UDP_glucuronic acid • Therapy: Phenobarbital Phototherapy (blue light)
Crigler –Najjar Syndrome Type I(congenital nonhemolytic jaundice) • Rare • Autosomal recessive • Severe congenital jaundice (bilirubin>20mg/dl) • Fatal within 15 months of life • Phototherapy
Crigler –Najjar Syndrome Type II • Rare • Inherited • More benign than type I • bilirubin<20mg/dl • Phenobarbital
Gilbert Syndrome • 30% of enzyme activity is preserved • Harmless
Toxic Hyperbilirubinemia • Toxin- induced liver dysfunction due to choloroform, arsphenamines, acetaminophen, carbon tetrachloride, hepatitis virus, cirrhosis Amanita mushroom poisoning