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The plot thickens: A pediatric cases series on collagenous gastritis
Annemarie Rompca1, Jessica Davis2, Ryan Pitman1
1Department of Gastroenterology, Hepatology and Nutrition Indiana University School of Medicine, Riley Hospital for Children Indianapolis Indiana USA.
Insights
Collagenous gastritis (CG) is a rare gastric disorder. This study highlights four pediatric cases, including the first reported identical twins with CG, emphasizing diagnostic and management challenges.
Area of Science:
- Gastroenterology
- Pediatric Gastroenterology
- Pathology
Background:
- Collagenous gastritis (CG) is a rare gastrointestinal disorder.
- Characterized by subepithelial collagen deposition in the gastric mucosa.
- Associated symptoms include anemia, abdominal pain, dyspepsia, vomiting, and weight loss.
Purpose of the Study:
- To present four cases of pediatric collagenous gastritis.
- To report the first known case of identical twins with collagenous gastritis.
- To discuss the diagnostic and management difficulties associated with CG.
Main Methods:
- Retrospective chart review.
- Analysis of four pediatric cases diagnosed with collagenous gastritis.
Main Results:
- All four patients presented with anemia.
- Three patients were initially misdiagnosed with eosinophilic gastritis.
- Most patients did not respond to conventional medication management.
Conclusions:
- Collagenous gastritis is a rare and challenging diagnosis.
- Effective management strategies for CG remain elusive.
- Further research is needed to improve diagnosis and treatment outcomes.
Objective:
Collagenous gastritis (CG) is a rare gastrointestinal disorder characterized by the deposition of collagen in the sub-epithelium of the gastric mucosa. CG can cause a variety of symptoms including iron deficiency anemia, abdominal pain, dyspepsia, vomiting, and weight loss. We present four cases of pediatric CG, and the first known reported case of identical twins with collagenous gastritis.
Methods:
This is a retrospective chart review of four cases of CG.
Results:
Four male patients all presented with anemia, three of which were initially diagnosed with eosinophilic gastritis. They were all eventually diagnosed with CG and most did not respond to medication management.
Conclusions:
CG is a rare disorder that is difficult to diagnosis and manage.
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