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Microscopic colitis in children with chronic diarrhea
Prashant Singh1, Prasenjit Das, A K Jain
1Department of Pediatrics, Center for Diarrheal Diseases and Nutrition Research, Indian Council of Medical Research, New Delhi, India.
Insights
Microscopic colitis (MC) was identified in children experiencing chronic diarrhea. This condition, characterized by specific mucosal biopsy changes, warrants further investigation into its prevalence in pediatric populations.
Area of Science:
- Pediatric Gastroenterology
- Gastrointestinal Pathology
Background:
- Chronic diarrhea in children can be challenging to diagnose.
- Microscopic colitis (MC) is an underrecognized cause of chronic diarrhea.
Purpose of the Study:
- To investigate the prevalence and characteristics of microscopic colitis in children with chronic diarrhea.
- To analyze mucosal biopsy changes associated with MC in pediatric patients.
Main Methods:
- 100 children (3-12 years) with chronic nonbloody diarrhea were screened.
- Colonoscopies and colonic biopsies were performed to identify lymphocytic colitis or collagenous colitis.
- Biopsies were compared between children with MC, chronic diarrhea without MC, and those with rectal bleeding.
Main Results:
- Microscopic colitis was diagnosed in 5 of 26 children with chronic diarrhea (3 lymphocytic colitis, 2 collagenous colitis).
- Children with MC showed significantly higher polymorphonuclear infiltration compared to control groups.
- Increased intraepithelial lymphocytes and basement membrane thickening were observed in MC patients.
Conclusions:
- Microscopic colitis is a relevant diagnosis in children presenting with chronic nonbloody diarrhea.
- Further multicenter studies are needed to establish the prevalence of pediatric microscopic colitis.
Objective:
The aim of the present study was to study microscopic colitis (MC) in children with special reference to its role in chronic diarrhea and changes in mucosal biopsies.
Methods:
A total of 100 consecutive children ages 3 to 12 years, with nonbloody diarrhea (passage of ≥3 loose stools per day) of >12 weeks' duration were screened and 26 were enrolled in the study in which no specific etiology could be found and colonoscopy did not reveal any mucosal abnormality. Colonic biopsies were evaluated for the presence of lymphocytic colitis or collagenous colitis and those with the characteristic changes were defined to have MC (group A). Colonic biopsies from patients with MC were compared with biopsies from patients with chronic diarrhea but no evidence of MC (group B). One hundred children ages 3 to 12 years with bleeding per rectum were screened and colonic biopsies from 45 patients (group C) who had colonic mucosal changes but no vascular or polyp lesion were compared with patients with MC.
Results:
Of the 26 patients with chronic diarrhea, MC was found in 5 (3 lymphocytic colitis and 2 collagenous colitis). Significantly higher polymorphonuclear infiltration was seen in group A as compared with group B (13.8 [5.4-20.6] vs 7.2 [0-19.6]; P = 0.03) or group C (13.8 [5.4-20.6] vs 4 [0-13.4]; P = 0.007). Intraepithelial lymphocytes (12 [4-32] vs 4 [0-24]; P = 0.008) and basement membrane thickening (3.5 [2.9-10.6] vs 2.5 [1.6-5.86]; P = 0.008) were also significantly higher in group A as compared with group C.
Conclusions:
MC was found to be present in children with nonbloody chronic diarrhea in children. Further multicentric studies may provide adequate data on its prevalence.
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