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Updated: Jul 8, 2026

Investigating Intestinal Inflammation in DSS-induced Model of IBD
Published on: February 1, 2012
Pediatric "PSC-IBD": a descriptive report of associated inflammatory bowel disease among pediatric patients with psc
W A Faubion1, E V Loftus, W J Sandborn
1Department of Internal Medicine and Pediatrics, Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota 55902, USA.
Insights
Inflammatory bowel disease (IBD) in children with primary sclerosing cholangitis (PSC) is common and often presents as pancolitis. Heightened surveillance for dysplasia and frequent pouchitis are indicated in these pediatric patients.
Area of Science:
- Pediatric Gastroenterology
- Hepatology
- Inflammatory Bowel Disease Research
Background:
- Adult inflammatory bowel disease (IBD) in primary sclerosing cholangitis (PSC) features pancolitis, rectal sparing, and risks of pouchitis and neoplasia.
- Clinical characteristics of IBD in pediatric PSC patients are not well-documented.
Purpose of the Study:
- To define the frequency, clinical features, and natural history of IBD in pediatric patients diagnosed with PSC.
Main Methods:
- Retrospective chart review of pediatric patients (≤18 years) diagnosed with PSC at Mayo Clinic (1975-1999).
- Recorded endoscopic, histologic, and surgical outcomes.
Main Results:
- 43 of 52 (84%) pediatric PSC patients had IBD (32 ulcerative colitis, 4 Crohn's disease).
- IBD was asymptomatic in 11%; 27% showed rectal sparing.
- Pouchitis complicated 4 of 5 ileal pouch-anal anastomoses; 3 proctocolectomies were for dysplasia.
Conclusions:
- IBD is common in pediatric PSC.
- Asymptomatic IBD can occur with PSC.
- Accelerated dysplasia risk necessitates heightened endoscopic surveillance in pediatric IBD-PSC patients.
- Pouchitis is a frequent complication.
Background:
Inflammatory bowel disease (IBD) in adults with primary sclerosing cholangitis (PSC) is characterized by pancolonic involvement, a high frequency of rectal sparing, and an increased risk of pouchitis and colorectal neoplasia. The clinical features of IBD in pediatric patients with PSC have not been well described. The aim of this study was to characterize the frequency, clinical features, and natural history of IBD in pediatric patients diagnosed with PSC.
Methods:
A retrospective chart review was performed for all patients 18 years of age or younger diagnosed with PSC seen at the Mayo Clinic between 1975 and 1999. Endoscopic and histologic features and surgical and postsurgical outcomes were recorded.
Results:
Fifty-two children with PSC were identified. Forty-three patients (84%) were also diagnosed with IBD. In 36 of 43 cases, there was a sufficient diagnostic evaluation to allow a detailed review. Thirty-two of 36 patients (89%) had ulcerative colitis and 4 of 36 patients (11%) had Crohn's disease. In 4 of 36 patients (11%), IBD was asymptomatic. Although the most frequent endoscopic presentation of IBD was universal colitis, endoscopic rectal sparing was frequently noted (27% of colonoscopic studies). Of the four patients diagnosed with Crohn disease, in none did perianal, fistulizing, or stricturing disease develop. Proctocolectomy was performed in six patients (17%); three operations were performed for dysplasia. Pouchitis complicated four of the five ileal pouch-anal anastomoses procedures.
Conclusions:
Among pediatric patients (1) PSC without IBD is uncommon; (2) asymptomatic IBD may be associated with PSC; (3) because the time to dysplasia may be accelerated, once the diagnosis of IBD is made in the setting of PSC, heightened endoscopic surveillance may be indicated; (4) pouchitis occurs frequently in these patients.
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