Sclerosing cholangitis associated to cryptosporidiosis in liver-transplanted children
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Updated: Oct 17, 2026

Isolation of Neonatal Extrahepatic Cholangiocytes
Published on: June 5, 2014
M Campos1, E Jouzdani, C Sempoux
1University of Louvain, Departement de Pédiatrie, Brussels, Belgium.
Insights
Cryptosporidium intestinal infection can cause unexplained cholangiopathies in pediatric liver transplant recipients. This serious complication may necessitate retransplantation, highlighting the importance of identifying intestinal parasite carriage.
Area of Science:
- Pediatric Gastroenterology and Hepatology
- Transplant Medicine
- Infectious Diseases
Background:
- Pediatric liver transplantation involves complex immunosuppression protocols.
- Post-transplant complications can include biliary issues and infections.
- Cryptosporidium is an opportunistic intestinal parasite.
Observation:
- Three pediatric liver transplant recipients developed diffuse cholangitis.
- All three patients had intestinal Cryptosporidium carriage and received tacrolimus and prednisone immunosuppression.
- No other infectious agents or vascular complications were identified.
Findings:
- Treatment with paromomycin and reduced immunosuppression resolved Cryptosporidium carriage in all patients.
- Bile duct reoperation was required for all three, with one developing biliary cirrhosis necessitating retransplantation.
- All patients are alive and free of parasitic infection post-treatment.
Implications:
- Intestinal Cryptosporidium infection should be considered in pediatric liver transplant recipients with unexplained cholangiopathy.
- Early diagnosis and management of Cryptosporidium can mitigate severe outcomes.
- This finding underscores the link between intestinal infections and graft health in pediatric liver transplant patients.
Unlabelled:
Three children of a series of 461 pediatric liver transplant recipients developed diffuse cholangitis associated with intestinal cryptosporidium carriage. All three received immunosuppression consisting of tacrolimus and prednisone. Cryprosporidium carriage was treated with paramomycin, while immunosuppression was decreased according to graft tolerance. No other infectious pathogens were found, and no vascular problems were detected. Bile duct anastomosis was reoperated in all three, but biliary cirrhosis developed in one patient, requiring retransplantation. All three patients are alive and well, and free of intestinal parasites on follow-up.
Conclusion:
Cryptosporidium intestinal infection may play a role in some cases of otherwise unexplained cholangiopathies in pediatric liver transplant recipients. This may lead to significant morbidity, including need for retransplantation.
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