CONGENITAL BILIARY ATRESIA
Congenital atresia
of the extrahepatic bile ducts is
the most
common
cause of prolonged obstructive jaundice in the
neonatal
period.
INCIDENCE
Biliary atresia occurs once in every
20,000 to 30,000 births.
PATHOLOGY
Failure of
recanalization of the ducts
which have no
lumen.
Coexistence of atresia of the
extrahepatic and entrahepatic ducts
supports the
belief that a development
anomaly is the
basic
defect.
The
procedure is an attempt to reduce
pressure the esophageal
veins by :
*
Devasularestion, the vessal
supplying the upper
greater
curvature (spleic bronchea) and
the lesser currature (left
gastric branches) are ligated
*
Shunt procedures like a spleno-renal anastamosis or an end to
side porto-caval an mesenteric vein and canal anastomosis can
also reduce pressure.
TREATMENT
Surgical operation to expolore the fibrous tissues at
the Porta
Hepatis and an anastomosis of bile channels with an
intestinal
loop provides an outlet for the bile.
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