Therapy of Caroli’s syndrome usually consists
of endoscopic stone removal in order to achieve adequate
bile flow and to avoid secondary complications
such as cholangitis or deterioration of liver function. If
primary endoscopic treatment is not sufficient, liver resection
or transplantation could become necessary to
achieve a stone-free situation. Case Report: We herein
describe a case of bilobular Caroli’s syndrome which was
primarily endoscopically treated. Due to a common bile
duct stricture after cholecystectomy and choledochotomy
10 years before, endoscopic stone removal was impossible.
Instead of liver resection or transplantation, we
performed a wide side-to-side choledochoduodenostomy
which allowed subsequent endoscopic treatment
with successful removal of all bile duct stones during repeated
sessions. Six years after surgery, no further
episodes of cholangitis have occurred, and the patient
has fully recovered with normal liver function. Conclusion:
Even bilobular Caroli’s syndrome refractory to primary
endoscopic treatment might be removed using an
interdisciplinary approach thereby successfully avoiding
liver resection or transplantation.