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Updated: May 7, 2026

Fluorescence-mediated Tomography for the Detection and Quantification of Macrophage-related Murine Intestinal Inflammation
Published on: December 15, 2017
Focally enhanced gastritis in newly diagnosed pediatric inflammatory bowel disease
Tetsuo Ushiku1, Christopher J Moran, Gregory Y Lauwers
1*Department of Pathology and Center for the Study of Inflammatory Bowel Disease, Massachusetts General Hospital and Harvard Medical School †Department of Pediatrics, Division of Pediatric Gastroenterology, Hepatology, and Nutrition, MassGeneral Hospital for Children, Boston, MA.
Insights
Focally enhanced gastritis (FEG) is more prevalent in pediatric Crohn disease (CD) than ulcerative colitis (UC), particularly in younger children. FEG in pediatric CD correlates with disease activity and granulomas.
Area of Science:
- Pediatric Gastroenterology
- Histopathology
- Inflammatory Bowel Disease
Background:
- Focally enhanced gastritis (FEG) significance in adult Crohn disease (CD) is debated.
- FEG may be a more specific marker for pediatric CD.
Purpose of the Study:
- To detail FEG histologic features in pediatric inflammatory bowel disease (IBD).
- To clarify the association between FEG and pediatric CD.
Main Methods:
- Reviewed gastric biopsies from 119 newly diagnosed pediatric IBD patients (62 CD, 57 UC) and 66 controls.
- Histology was reviewed blinded to diagnosis.
- Compared FEG prevalence, morphology, and association with other GI findings.
Main Results:
- FEG found in 43% of pediatric IBD (55% CD vs. 30% UC) and 5% of controls.
- FEG more common in younger CD patients (peak 5-10 years).
- FEG in CD associated with active ileitis and granulomas; no such link in UC.
Conclusions:
- FEG frequency, morphology, and association with other lesions differ between pediatric CD and UC.
- FEG is linked to disease activity and granulomas in pediatric CD.
Abstract:
Although the significance of focally enhanced gastritis (FEG) as a marker of Crohn disease (CD) in adults has been contested, several studies suggest that it may be more specific of CD in pediatric patients. This study describes the detailed histologic features of FEG in pediatric inflammatory bowel disease (IBD) and clarifies its association with CD. A series of 119 consecutive newly diagnosed IBD patients (62 CD cases, 57 ulcerative colitis [UC] cases) with upper and lower gastrointestinal biopsies were evaluated. The histology of the gastric biopsies was reviewed blinded to final diagnoses and compared with age-matched healthy controls (n=66). FEG was present in 43% of IBD patients (CD 55% vs. UC 30%, P=0.0092) and in 5% of controls. Among CD patients, FEG was more common in younger patients (73% in children aged 10 y and below, 43% in children above 10 y of age, P=0.0358), with the peak in the 5- to 10-year age group (80%). The total number of glands involved in each FEG focus was higher in UC (6.4±5.1 glands) than in CD (4.0±3.0 glands, P=0.0409). Amongst the CD cohort, patients with FEG were more likely than those without FEG to have active ileitis (79% vs. 40%, P=0.0128) and granulomas elsewhere in the gastrointestinal tract (82% vs. 43%, P=0.0016). There was no correlation between FEG and other gastrointestinal findings of UC. We demonstrate that differences in FEG seen in pediatric CD and UC relate to not only their frequencies but also the morphology and relationship with other gastrointestinal lesions. Further, FEG is associated with disease activity and the presence of granulomas in pediatric CD.
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