Related Experiment Video
Updated: Apr 28, 2026

Isolation of Neonatal Extrahepatic Cholangiocytes
Published on: June 5, 2014
Prolonged, but transient, elevation of liver and biliary function tests in a healthy infant affected with breast milk
Dimitri Poddighe1, Lucia Castelli1, Gian Luigi Marseglia2
1Department of Pediatrics, Ospedale di Circolo di Melegnano, Vizzolo Predabissi, Italy.
Insights
Neonatal jaundice, specifically breast milk jaundice, can unexpectedly elevate liver enzymes. In asymptomatic infants, prolonged monitoring is recommended over extensive testing for severe conditions.
Area of Science:
- Neonatology
- Pediatric Gastroenterology
- Clinical Biochemistry
Background:
- Unconjugated hyperbilirubinaemia is common in newborns and often requires investigation for underlying conditions.
- Breast milk jaundice is typically benign, associated with breastfeeding, and lacks other clinical or laboratory abnormalities.
Observation:
- A case of breast milk jaundice presented with unexpectedly elevated plasma liver and biliary enzymes.
- The infant remained clinically well with appropriate growth despite abnormal liver function tests.
Findings:
- Extensive investigations ruled out metabolic, infectious, and autoimmune liver diseases.
- Liver function tests normalized spontaneously between 6-7 months of age.
Implications:
- Suggests prolonged monitoring (6-7 months) for elevated liver enzymes in asymptomatic infants with breast milk jaundice.
- Advocates for delaying sophisticated diagnostic investigations for unlikely severe diseases in such cases.
Abstract:
Unconjugated hyperbilirubinaemia is a common finding in newborns. When it is exaggerated, it is usually investigated in order to exclude several diseases, such as newborn's haemolytic diseases, infections or hypothyroidism. Breast milk jaundice is a form of neonatal jaundice related to breast feeding and it is not usually associated with any clinical issue and/or other laboratory abnormalities. We describe a case of breast milk jaundice being associated, unexpectedly, to significant elevation of plasmatic liver and biliary enzymes. Despite the infant's good clinical condition and growth, several investigations were performed and these ruled out metabolic, infectious and autoimmune liver diseases. All liver function tests normalised by 6-7 months of life. We suggest that the finding of hypertransaminasaemia and hyper-γ-glutamyl transpeptidase in a benign clinical context (similar to what we described) should be followed for 6-7 months before performing sophisticated and expensive diagnostic investigations which aim at excluding some unlikely and severe diseases in a completely asymptomatic infant.
Related Concept Videos
Jaundice
Effect of Hepatic Disease on Pharmacokinetics: Pathophysiologic Assessment and Liver Function Test
Diseases of the Liver and Gallbladder
Cirrhosis is characterized by the scarring of hepatic lobules in the liver, which are replaced by fibrous tissue, affecting the liver's normal functioning. NAFLD, on the other hand, is caused by an excessive build-up of fat in the liver, not...
Pharmacokinetics in Pediatric Patients: Drug Metabolism
Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption
Inborn Errors of Metabolism

