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Congenital choledochal cyst is a rare disease, especially in fetal life and early infancy age.
Our case was a 66 days old female baby who had the symptoms of jaundice, clay-colored
stool, intermittent vomiting since birth and abdominal distension.
Final diagnosis was choledochal cyst with neonatal hepatitis.
An early accurate preoperative diagnosis has been associated with a marked decrease in the
mortality.
Roux-en-Y choledochocystojejunostomy was done.
We... |
