IPLab:Lab 13:Biliary Atresia

Clinical Summary

This eight-month-old female developed jaundice at one week of age. As the jaundice deepened, the child's bilirubin level was found to be over 30 mg/dL and the patient experienced a few convulsive episodes. A liver biopsy produced a diagnosis of extrahepatic bile duct obstruction. A subsequent exploratory laparotomy showed an absence of extrahepatic bile duct structures--including the gallbladder--and an intraoperative cholangiogram failed to show any large biliary channel. A jejunohepatostomy in the portal area was performed in the hope of establishing bile drainage and the patient was placed on the waiting list for a liver transplant. However, the patient progressively deteriorated, developed infections, and after a long turbulent course, died of pneumonia.

Images

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  This is a low power photomicrograph of a section of liver. Even at this low magnification, areas of fibrosis can be appreciated.

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  This medium-power photomicrograph of liver shows an area of portal fibrosis and bile duct proliferation (arrows). Adjacent to this fibrotic portal region, hepatocytes are seen separated by dilated sinusoids. Throughout this section are found accumulations of yellow-brown bile pigment.

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  This high-power photomicrograph of fibrotic portal region demonstrates proliferation of the bile ducts (arrows).

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  This is a high-power photomicrograph of fibrotic portal region with several bile ducts that contain inspissated bile (arrows). Adjacent hepatocytes also contain bile pigments.

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  This is a medium-power photomicrograph of liver section stained with a trichrome stain to demonstrate the portal fibrosis. The fibrous connective tissue (collagen) stains blue.

Study Questions

• How common is biliary atresia?

Biliary atresia occurs in approximately 1 out of 10,000 live births.

• What are the usual presenting signs?

Neonatal cholestasis.

A major cause of neonatal cholestasis (1/3 of cases) is extrahepatic biliary atresia (EHBA).

• What is the pathogenesis of biliary atresia?

In most cases of EHBA the infants are born with a normal biliary tree. However, within the first few weeks of life the bile ducts are destroyed.

There are numerous theories as to the etiology of the inflammatory process that destroys the bile ducts in these newborns. These include:

1. viral infections (reovirus 3, cytomegalovirus, and rubella virus);
2. genetic inheritance (EHBA has been reported in twins and there are descriptions of EHBA occurring in families with anomalies of the intrahepatic biliary tree); and
3. abnormal embryologic development--15 to 20% of EHBA patients have extrahepatic anomalies such as polysplenism, cardiovascular defects, and bowel atresias.

• What is the standard treatment for extra-hepatic biliary atresia?

Liver transplantation.

Additional Resources

Reference

• eMedicine Medical Library: Pediatric Biliary Atresia
• Merck Professional: Neonatal Cholestasis