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Articles in Kansai Surgery
The "golden" phase of treatment of biliary atresia in infants
Congenital biliary atresia is a rare disease of the liver and biliary tract, characterized by disruption or deficiency of the extrahepatic biliary system, causing obstruction of bile flow. Due to misdiagnosis and late detection, many infants are missed the golden opportunity to have surgery to treat the disease. So when is the best time to treat congenital biliary atresia?
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Distinguishing congenital biliary atresia from physiological jaundice, anemia, hepatitis
Jaundice in newborns is a manifestation of one of the diseases such as anemia, hepatitis or physiological jaundice or even congenital biliary atresia. The distinction between these diseases is to determine the direction of treatment for the child.
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Congenital biliary atresia: Intractable disease
According to statistics, about 50-80% of newborns with congenital biliary atresia, if not treated well, will die of biliary cirrhosis when the child is 1 year old. This percentage will increase to about 90 - 100% by the time a child is 3 years old. Therefore, if the child shows signs of suspected congenital biliary atresia, the family should immediately take the child to the hospital for examination and timely diagnosis.
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Complications of congenital biliary dilatation
Congenital dilatation of the biliary tree is one of the most common inherited liver diseases, especially in Asian countries. Complications of congenital biliary dilatation is a very complex disease, to accurately detect and diagnose this pathology, it is necessary to combine clinical symptoms and paraclinical support to strengthen the diagnosis.
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Complications after surgery for congenital biliary atresia
Congenital biliary atresia is considered a rare pathology of the liver and biliary tract, characterized by disruption or deficiency of the extrahepatic biliary system, resulting in obstruction of bile flow.
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