Background: The accuracy of the technique of antenatal ultrasonography
in the diagnosis of congenital bile duct lesions is unknown. Methods:
Thirteen patients with proven biliary disease who had abnormal antena
tal scans were reviewed. Two infants had type I cystic biliary atresia
and one had a noncommunicating segmental dilatation of the bile duct
in a type 3 biliary atresia. The remainder had choledochal cysts and i
ncluded two patients with intrahepatic cysts. The correct diagnosis wa
s made antenatally in only two (15%) cases. Of the remaining patients,
seven received a diagnosis of intraabdominal cysts of unknown etiolog
y, three of duodenal atresia, and one ovarian cyst. The median gestati
onal age at the antenatal diagnosis was 20 weeks. Results: Jaundice de
veloped in 11 infants, and dilatation of intrahepatic biliary radicals
was noted in four of the choledochal cysts. Obstructive jaundice and
increasing cyst size were indications for early surgery, and twelve in
fants underwent a laparotomy at a median age of 4 weeks. During the me
dian follow-up period of 2 years, 12 of the 13 patients have lost thei
r jaundice or remained anicteric. Antenatal diagnosis offers the possi
bility of early definitive surgery for uncomplicated choledochal dilat
ation and the chance of improved outcome for surgically treated biliar
y atresia. An algorithm is suggested for the management of antenatally
detected cystic biliary lesions. Copyright (C) 1998 by W.B. Saunders
Company.