Differential diagnostics of jaundice

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Normal bilirubin values are 2.0–17.0 µmol/L. If serum bilirubin levels rise above approximately 20 μmol/l, we speak of hyperbilirubinemia. At higher levels, bilirubin starts to accumulate in the tissues, subicterus develops (yellow discoloration of the parts of the sclera covered by the lids, soft palate; serum bilirubin around 30–80 μmol/l), and then icterus (jaundice). Pathologies from a low level of bilirubin are not described, physiologically the total bilirubin in the blood is mainly represented by unconjugated bilirubin. The terms "direct" and "indirect" bilirubin come from Van den Bergh, according to the method of determination. Approximately, direct = conjugated, indirect = non-conjugated. Only conjugated bilirubin can be found in urine, whereas only unconjugated can deposit in the CNS tissue when the blood-brain barrier is immature or damaged (in newborns kernicterus). According to the etiology, we distinguish the following types of hyperbilirubinemia and jaundice:

  • non-conjugated – increased supply of bilirubin, the process of conjugation in the liver can't keep up,
  • conjugated – impaired excretion into bile
  • mixed.

Hyperbilirubinemia with predominantly non-conjugated bilirubin[edit | edit source]

Hyperbilirubinemia caused by increased bilirubin production[edit | edit source]

Discoloration of sclera in jaundice patient

Icterus neonatorum (neonatal jaundice)[edit | edit source]

Neonatal jaundice
  • In addition to hemolysis, the immaturity of conjugating enzymes in the liver also plays a role;
  • in the first five days, it occurs in almost half of newborns (70–80 μmol/l);
  • breast-fed newborns have higher levels (UGTA1 enzyme inhibitor in milk) – it is not usually associated with neurological damage
  • other problems are, for example, with erythroblastosis fetalis, ABO incompatibility…;
  • pathological jaundice – already within 24 hours after birth, above 220 μmol/l;
  • phototherapy – breakdown of bilirubin in the skin with 425–475 nm light – photoisomers are polar (they are no longer dangerous for the CNS).

Hyperbilirubinemia with reduced conjugation[edit | edit source]

Gilbert syndrome[edit | edit source]
  • Chronic, small elevation of bilirubin, usually no more than 50–70 μmol/L, subicterus only, decreased hepatic UGTA1 activity (TATA box disorder, decreased expression, AD, 10–12 % population);
  • often diagnosed incidentally;
  • bilirubin acts as a scavenger of free radicals, hyperbilirubinemia protects against oxidative stress.
Crigler-Najjar syndrome[edit | edit source]
  • AR, complete (type I) or partial (type II) UGTA defect;
  • in type I conjugated bilirubin is completely absent, unconjugated bilirubin levels are around 300–800 μmol/l;
  • icterus appears shortly after birth, without phototherapy individuals soon die of CNS involvement;
  • in type II – concentration of approx. 350 μmol/l.

Hyperbilirubinemia with predominantly conjugated bilirubin[edit | edit source]

Hyperbilirubinemia caused by impaired secretion[edit | edit source]

Dubin-Johnson syndrome[edit | edit source]

  • Benign, AR, symptoms: only jaundice;
  • for an unknown reason, coproporphyrin I is increased in the urine;
  • a defect in the canalicular system by which bilirubin is secreted from hepatocytes.

Rotor syndrome[edit | edit source]

  • Also rare, similar to the previous one.

Hyperbilirubinemia caused by bile outflow disorder[edit | edit source]

Intrahepatic cholestasis[edit | edit source]

  • A number of drugs – estrogens, steroids, some ATB…;
  • bile acids and liver enzymes are also increased in the blood.


Links[edit | edit source]

Related articles[edit | edit source]

Source[edit | edit source]

Bibliography[edit | edit source]

  • HAVLÍK, Jiří, et al. Infektologie. 2. edition. Praha : Avicenum, 1990. 293 pp. ISBN 80-201-0062-8.
  • LOBOVSKÁ, Alena. Infekční nemoci. 1. edition. Praha : Karolinum, 2001. 263 pp. ISBN 80-246-0116-8.