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Jaundice

Jaundice: Excerpt from Pediatric Complaints and Diagnostic Dilemmas

Eric J. Frehm

Approach to the Patient with Jaundice

I. Definition of the Complaint

Jaundice is the yellow discoloration of the skin, mucous membranes, and sclerae that is caused by increased serum levels of bilirubin, a byproduct of heme breakdown. As a lipophilic pigment, bilirubin must bind to plasma albumin for carriage to the liver. It is taken up by hepatocytes for conjugation with solubilizing sugars to form bilirubin diglucuronides (and, less commonly, monoglucuronides), thus allowing for excretion into bile. Not all jaundice is pathologic. Indeed, the vast majority of clinically encountered hyperbilirubinemia occurs as physiologic jaundice in neonates.

II. Complaint by Cause and Frequency

Neonatal jaundice can be caused by conjugated or unconjugated hyperbilirubinemia (Table 15-1). The differential diagnosis of cholestatic jaundice in the older child differs from diseases that present early in life. Young infants are more likely to have congenital anatomic anomalies, such as biliary atresia, or inborn metabolic disorders, such as galactosemia. Older children are more likely to experience acquired or secondary liver diseases, such as autoimmune or toxic hepatitis, or liver impairment related to inflammatory bowel disease. Infectious hepatitis is among the most common causes of liver disease in older children and adolescents. Viruses causing hepatitis and jaundice in these children include: hepatitis A, B, C, D and E; Epstein-Barr virus; cytomegalovirus; varicella; human herpesvirus 6 (HHV-6); and herpes simplex virus (HSV). Other infectious diseases associated with jaundice include schistosomiasis, leptospirosis, Rocky Mountain spotted fever, ehrlichiosis, and malaria.
Obstructive, extrahepatic causes of conjugated hyperbilirubinemia in children and adolescents to consider include cholelithiasis, choledochal cysts, sclerosing cholangitis, pancreatitis, and tumors and other anatomic abnormalities along the choledocho-pancreatico-duodenal path.

III. Clarifying Questions

• Is the elevated bilirubin level all unconjugated? Is the process a conjugated hyperbilirubinemia?
 — Separating a total bilirubin measurement into its conjugated and unconjugated components is a critical step in the evaluation of hyperbilirubinemia in a child. Conjugated hyperbilirubinemia is present when the conjugated fraction is at least 1.5 mg/dL or accounts for more than 15% of the total bilirubin measurement. Conjugated hyperbilirubinemia is abnormal and merits prompt evaluation, particularly in infants, in whom diseases such as biliary atresia require urgent therapy. An increased unconjugated bilirubin level suggests a very different differential diagnosis but can also be a medical emergency if very high: unconjugated bilirubin is able to cross the blood-brain barrier and directly injure the brain.
Sometimes the terms “direct” and “indirect” bilirubin are used interchangeably with the terms “conjugated” and “unconjugated.” The former terms derive from the van den Bergh reaction, in which the conjugated bilirubin component is measured directly (by colorimetric analysis after reaction with a diazo compound). The subsequent addition of methanol allows for a measurement of total bilirubin, after which unconjugated fraction is determined indirectly, by subtracting the conjugated bilirubin level from the total bilirubin level. Of note, measurement of the direct bilirubin fraction detects not just bilirubin diglucuronides and monoglucuronides but also “delta” bilirubin, which forms when conjugated bilirubin seeps retrograde into the serum and binds covalently to albumin. Because of the delta component 's long half-life, the “direct fraction” can remain deceptively elevated even as a conjugated hyperbilirubinemia improves.
• Does the jaundiced baby have other concerning physical findings?
 — A significant unconjugated hyperbilirubinemia can result from the increased bilirubin of a cephalohematoma or extensive bruising. A newborn afflicted with a TORCH infection might have microcephaly, growth retardation, hepatosplenomegaly, chorioretinitis, or petechiae. A heart murmur is often heard in children with Alagille syndrome, whereas a baby with Zellweger syndrome is hypotonic and dysmorphic. Of course, serious bacterial infection must always be considered in any case of significant bilirubinemia.
• Is there a family history of jaundice?
— Many of the disorders that manifest with jaundice are heritable. α1-Antitrypsin deficiency, Crigler-Najjar syndrome type I and II, galactosemia, and tyrosinemia are just a few of the autosomal recessive diseases associated with neonatal jaundice. On the other hand, Alagille syndrome is an autosomal dominant disorder (but with variable penetrance and expressivity). The inheritance of glucose-6-phosphate dehydrogenase (G6PD) deficiency is X-linked but so highly polymorphic that it should be considered in the evaluation of boys and girls alike.
• Were there changes in the child's diet or other new “exposures” that preceded the onset of jaundice?
 — Deficiencies in the metabolism of galactose or fructose can lead to jaundice in infants. Likewise, children with G6PD deficiency can have hemolytic crises triggered by certain foods (e.g., fava beans), medications (e.g., antimalarial agents), or other compounds (e.g., mothballs).
• Are neonatal hyperbilirubinemia risk factors present?
 — Risk factors for neonatal jaundice that derive from the mother include ethnicity (e.g., Asian, Native American) and pregnancy complications such as gestational diabetes or blood group incompatibility. Birth trauma that results in extravascular blood collections is also a risk factor for jaundice. Other independent risk factors for the infant include polycythemia, prematurity, breast-feeding, perinatal infections, and a long, heterogenous list of genetic disorders.

IV. References

 1. D'Agata ID, Balistreri WF. Evaluation of liver disease in the pediatric patient. Pediatr Rev 1999;20:376–389.
2. Dennery PA, Seidman DS, Stevenson DK. Neonatal hyperbilirubinemia. N Engl J Med 2001;344:581–590.
3. Gourley GR. Neonatal jaundice and disorders of bilirubin metabolism. In: Suchy FJ, Sokol RJ, Balistreri WF, eds. Liver disease in children, 2nd ed. Philadelphia: Lippincott Williams & Wilkins, 2001:275–314.
4. Maisels MJ. Jaundice. In: Avery GB, Fletcher MA, MacDonald MG, eds. Neonatology: pathophysiology and management of the newborn, 5th ed. Philadelphia: Lippincott Williams & Wilkins, 1999:765–819.
5. Maller ES. Jaundice. In: Altschuler SM, Liacouris CA. Clinical pediatric gastroenterology. New York: Churchill Livingstone, 1998:49–61.

Pictures

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Book Source Details

  • Book Title: Pediatric Complaints and Diagnostic Dilemmas
  • Author(s): Samir S Shah MD; Stephen Ludwig MD
  • Year of Publication: 2003
  • Copyright Details: Pediatric Complaints and Diagnostic Dilemmas, Copyright © 2003 Lippincott Williams & Wilkins.

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Copyright notice for book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.




More About This Book:
Title: Pediatric Complaints and Diagnostic Dilemmas
Authors: Samir S Shah MD; Stephen Ludwig MD
Publisher: Lippincott Williams & Wilkins
Copyright: 2003
ISBN: 0-7817-4188-2

 » Next page: Jaundice - Case 15-3: 2-Month-Old Boy (Pediatric Complaints and Diagnostic Dilemmas)

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