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Published on: February 28, 2025
Reversible sclerosing cholangitis with ulcerative colitis.
Keisuke Kakisaka1, Kazuyuki Ishida2, Kojiro Kataoka1
1Division of Hepatology, Department of Internal Medicine, Iwate Medical University, Morioka, Japan.
Sclerosing cholangitis with granulocytic epithelial lesions (GEL) shows positive response to immunosuppression. This case highlights successful treatment of GEL-positive SC using prednisolone, leading to significant clinical and histological improvements.
Area of Science:
- Hepatology
- Gastroenterology
- Immunology
Background:
- Sclerosing cholangitis (SC) is a chronic liver disease characterized by bile duct inflammation and fibrosis.
- Granulocytic epithelial lesions (GEL) are a specific histological finding within the bile ducts, often associated with SC.
- Ulcerative colitis (UC) is an inflammatory bowel disease that can sometimes be associated with liver manifestations like SC.
Observation:
- A 42-year-old female with active ulcerative colitis presented with elevated alkaline phosphatase and dilated intrahepatic bile ducts.
- Liver biopsy confirmed granulocytic epithelial lesions (GEL) with neutrophil infiltration into the bile duct epithelium.
- Treatment with prednisolone (PSL) was initiated due to active ulcerative colitis.
Findings:
- Prednisolone therapy led to a dramatic decrease in abnormal laboratory values.
- Follow-up liver biopsy showed resolution of neutrophil infiltration in the bile duct epithelium.
- Immunohistochemical analysis revealed no IgG4-positive plasma cells, differentiating it from IgG4-related sclerosing cholangitis.
Implications:
- This case demonstrates the efficacy of immunosuppression, specifically prednisolone, in treating SC with GEL.
- It provides valuable insights into treatment-induced histological changes and serial biochemical data during immunosuppressive therapy for this rare condition.
- The findings suggest that GEL-positive SC may be a distinct entity responsive to targeted immunosuppression.
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