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Biliary atresia

Biliary atresia is a rare condition in newborn children in which the biliary tract between the liver and the intestine is blocked or absent. If unrecognised, the condition leads to liver failure but not (as one might think) to kernicterus. It has no known cause, and the only effective treatment is by surgery. more...

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Symptoms and diagnosis

Initially, the symptoms are indistinguishable from neonatal jaundice, a common phenomenon. Prolonged jaundice that is resistant to phototherapy and/or exchange transfusions should prompt a search for secondary causes. By this time, liver enzymes are generally measured, and these tend to be grossly deranged, hyperbilirubinaemia is conjugated and therefore does not lead to kernicterus. Ultrasound investigation or other forms of imaging can confirm the diagnosis.

Pathophysiology

There is no known cause of biliary atresia, although it may be associated with a number of rare syndromes, such as malrotation of the intestine.

As the biliary tract cannot transport bile to the intestine, bile is retained in the liver and results in damage and the ultimate destruction of that organ.

Treatment

If the intrahepatic biliary tree is unaffected, surgical reconstruction of the extrahepatic biliary tract is possible.

If the atresia is complete, only liver transplantation is a therapeutic option.

Links

E-medicine overview

Intro. to pediatric blood tests for liver function

Research Links

Choledochal cyst associated with extrahepatic bile duct atresia

Support groups

Biliary Atresia Network

Children's Liver Association for Support Services

Liver Families

Read more at Wikipedia.org


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Biliary atresia
From Gale Encyclopedia of Medicine, 4/6/01 by J. Ricker Polsdorfer

Definition

Biliary atresia is the failure of a fetus to develop an adequate pathway for bile to drain from the liver to the intestine.

Description

Biliary atresia is the most common lethal liver disease in children, occurring once every 10,000-15,000 live births. Half of all liver transplants are done for this reason.

The normal anatomy of the bile system begins within the liver, where thousands of tiny bile ducts collect bile from liver cells. These ducts merge into larger and larger channels, like streams flowing into rivers, until they all pour into a single duct that empties into the duodenum (first part of the small intestine). Between the liver and the duodenum this duct has a side channel connected to the gall bladder. The gall bladder stores bile and concentrates it, removing much of its water content. Then, when a meal hits the stomach, the gall bladder contracts and empties its contents.

Bile is a mixture of waste chemicals that the liver removes from the circulation and excretes through the biliary system into the intestine. On its way out, bile assists in the digestion of certain nutrients. If bile cannot get out because the channels are absent or blocked, it backs up into the liver and eventually into the rest of the body. The major pigment in bile is a chemical called bilirubin, which is yellow. Bilirubin is a breakdown product of hemoglobin (the red chemical in blood that carries oxygen). If the body accumulates an excess of bilirubin, it turns yellow (jaundiced). Bile also turns the stool brown. Without it, stools are the color of clay.

Causes & symptoms

It is possible that a viral infection is responsible for this disease, but evidence is not yet convincing. The cause remains unknown.

The affected infant will appear normal at birth and during the newborn period. After two weeks the normal jaundice of the newborn will not disappear, and the stools will probably be clay-colored. At this point, the condition will come to the attention of a physician. If not, the child's abdomen will begin to swell, and the infant will get progressively more ill. Nearly all untreated children will die of liver failure within two years.

Diagnosis

The persistence of jaundice beyond the second week in a newborn with clay-colored stools is a sure sign of obstruction to the flow of bile. An immediate evaluation that includes blood tests and imaging of the biliary system will confirm the diagnosis.

Treatment

Surgery is the only treatment. Somehow the surgeon must create an adequate pathway for bile to escape the liver into the intestine. The altered anatomy of the biliary system is different in every case, calling upon the surgeon's skill and experience to select and execute the most effective among several options. If the obstruction is only between the gall bladder and the intestine, it is possible to attach a piece of intestine directly to the gall bladder. More likely, the upper biliary system will also be inadequate, and the surgeon will attach a piece of intestine directly to the liver--the Kasai procedure. In its wisdom, the body will discover that the tiny bile ducts in that part of the liver are discharging their bile directly into the intestine. Bile will begin to flow in that direction, and the channels will gradually enlarge. Survival rates for the Kasai procedure are not impressive--50% at five years, 15% at 10 years--but certainly better than no treatment at all. Persistent disease in the liver gradually destroys the organ.

Liver transplantation must be anticipated in all but the few patients who continue to do well after a Kasai procedure. Accumulating experience and newer techniques of liver transplantation are producing very gratifying early results.

Prognosis

Before liver transplants became available, even prompt and effective surgery did not cure the whole problem. Biliary drainage can usually be established, but the patients still have a defective biliary system that develops progressive disease and leads to an early death. Transplantation now achieves up to 90% one-year survival rates and promises to prevent the chronic disease that used to accompany earlier procedures.

Prevention

The specific cause of this birth defect is unknown, so all that women can do is to practice the many general preventive measures, even before they conceive.

Key Terms

Duodenum
The first part of the small intestine, beginning at the outlet of the stomach.
Hemoglobin
The red, iron-containing chemical in the blood that carries oxygen to the tissues.
Jaundice
The yellow color taken on by a patient whose liver is unable to excrete bilirubin. A normal condition in the first week of life due to the infant's delayed ability to process certain waste products.
Kernicterus
A potentially lethal disease of newborns caused by excessive accumulation of the bile pigment bilirubin.

Further Reading

For Your Information

    Books

  • Balistreri, William F. "Cholestasis." Nelson Textbook of Pediatrics Waldo E. Nelson, et al., ed. Philadelphia: W. B. Saunders, 1996, pp.1133-37.
  • Feldman, Mark, et al. "Diseases of the bile ducts." Sleisenger & Fordtran's Gastrointestinal and Liver Disease Philadelphia: W.B. Saunders, 1998, pp. 912-914.

    Periodicals

  • Ryckman, F., R. Fisher, and S. Pedersen, et al. "Improved survival in biliary atresia patients in the present era of liver transplantation." Journal of Pediatric Surgery 28 (1993): 382.

Gale Encyclopedia of Medicine. Gale Research, 1999.

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