We present a classic but rare case of spontaneous perforation of the bile d
uct in infancy and a previously undescribed treatment technique. The patien
t, a male age 5 weeks, was admitted with abdominal distention, ascites, and
conjugated hyperbilirubinemia. Ultrasound revealed ascites but did not pro
vide visualization of the gallbladder. Although hepatobiliary scintigraphy
with technetium [dimethyl iminodiacetic acid (HIDA scan)] showed normal upt
ake peritoneal excretion suggested perforation of the common bile duct (CBD
). Exploratory laparotomy revealed 200 cm(3) dark amber ascitic fluid in th
e peritoneal cavity and cholestasis of the liver. Intraoperative cholangiog
ram performed via the gallbladder showed a large perforation at the cystic
duct/CBD junction. The perforation was large and leakage of contrast preven
ted demonstration of the distal CBD despite our attempt to primarily repair
the perforation. The CBD was explored; a T-tube was placed. T-tube cholang
iogram demonstrated flow of contrast into the duodenum. A large leak remain
ed at the cystic CBD junction. A cholecystectomy was performed and a vascul
arized flap of the gallbladder wall was used to repair the CBD over the T-t
ube. The T-tube was clamped intermittently beginning 3 weeks postoperativel
y. T-tube cholangiogram performed 6 weeks postoperatively revealed no extra
vasation and normal intra- and extrahepatic biliary tree. The T-tube was su
bsequently discontinued and liver function tests remained normal at 6 month
s follow-up.