Introduction: Hepatolithiasis
characterized by the development of pigmented stones, composed of calcium
bilirubinate and, to a lesser extent, cholesterol, in the intrahepatic bile
ducts before their confluence with the common hepatic duct, regardless of the
coexistence of gallstones in the common bile duct or gallbladder.
Clinical case: A 40-year-old male
presented with abdominal pain of five months' duration, characterized by
epigastric pain and dyspepsia. Jaundice, nausea, pruritus, choluria, and
acholia were also present. An ultrasound revealing a gallbladder measuring 54x32x29
mm with a 3.2 mm wall. Multiple hyperechoic images projecting a posterior
acoustic shadow, with a stone measuring 19.6 mm. There was no dilation of the
intrahepatic bile ducts. Abnormal liver function tests were performed. ERCP
revealing a stone measuring 15 mm in diameter at the common hepatic duct. It
was impossible to extract the stone with papilla dilation, so the decision to
place a 10 Fr plastic stent, and bile duct exploration as a decisive
therapeutic method was recommended. Initiated laparoscopic cholecystectomy, a
catheter was introduced into the cystic duct, and intraoperative
cholangiography was performed, revealing a filling defect at the left hepatic
duct, as well as multiple distal stones and a variable double right hepatic
duct.
Discussion: Treatment of hepatolithiasis
consists of stone extraction plus adjuvant drug therapy. Cholangitis usually
coexists with hepatolithiasis; therefore, antibiotic therapy is necessary. For
nonsurgical stone removal, PTCL or ERCP are used. Although a noninvasive
approach is a promising treatment, the recurrence of hepatolithiasis is 20%.
When hepatolithiasis coexists with bile duct strictures, which occurs in 40% of
cases, since in these patients after PTCL or ERCP, the recurrence rate reaches
up to 51%.