Carolis Disease Presents as Acute Cholangitis and Recurrent Jaundice: A Case Report

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Authors: Mohammed Elamin Elsidig Mohammed Elsirag, Dr. Adeel Afzal, Elfatih Elsiddig Hagelamin, Mahir Khiralla
Cited by: 0
References: 10

Abstract

Background: Carolis disease is a rare congenital disorder characterized by dilatation of intrahepatic bile ducts, bile stasis, and bacterial infections. While frequent episodes of cholangitis are common in Carolis disease, it represents a lifethreatening condition that might lead to sepsis and multi-organ failure if left untreated. The presentation of disease may vary from abdominal pain, cholangitis, or end-stage liver disease, an enlarged liver is usually seen. Carolis disease is type V in Todanis classification of choledochal cysts, which categorizes them into five types based on their characteristics and anatomical involvement. The Global prevalence was less than 1 in 100,000 births. Male-to-female ratio 1:1.8. Age at diagnosis: Most patients present before age 30. Familial occurrence tends to be sporadic, but familial cases occur in 10-20 present of cases. We present a case of Carolis disease with cholangitis, highlighting the diagnostic approach, clinical course, and treatment strategies. Carolis disease is often misdiagnosed as uncertain cholestasis until complications like cholangitis occur. ERCP contrast injection can trigger cholangitis in patients with biliary dilatation. We advise limiting ERCP use to therapeutic purposes and employing lowpressure contrast techniques when necessary. Case Presentation: We present a case of a 41-year-old male with a long history of recurrent jaundice and a cholecystectomy 10 years ago, who came to the emergency room with a 6-day complaint of fever, right upper quadrant abdominal pain, and jaundice. Radiological studies showed the characteristic dilation of the bile duct, leading to the diagnosis of Carolis disease. The patient commenced on fluid resuscitation, IV antibiotics Cefotaxime, and was followed by biliary drainage via stent placed by ERCP, along with administration of ursodeoxycholic acid. Conclusion: This case displays the importance of considering Carolis disease in the differential diagnosis of patients with recurrent episodes of acute cholangitis.

Fields of Study & Subjects

Pediatric Hepatobiliary Diseases and Treatments Gallbladder and Bile Duct Disorders Liver Diseases and Immunity

Publication details

Journal / source
International Journal of Advanced Medical Sciences and Technology
Volume
6
Issue
2
Pages
1–4
Publication date
27 February 2026
Language
EN