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Author Spotlight: Investigating the Pathophysiology of Eosinophilic Esophagitis
Published on: May 10, 2024
Successful Montelukast Treatment in an Infant with Steroid-Resistant Eosinophilic Colitis
Nai-Wei Wang1, Hsuan Hsieh2, Yao-Jong Yang2
1Hull York Medical School, Allam Medical Building, University of Hull, Hull, United Kingdom.
Insights
This case report details an infant with steroid-resistant eosinophilic colitis (EC). Combined therapy with montelukast and ketotifen successfully treated the condition, leading to healthy growth.
Area of Science:
- Gastroenterology
- Pediatrics
- Immunology
Background:
- Eosinophilic gastrointestinal disorders (EGID) are characterized by eosinophil-predominant inflammation.
- Eosinophilic colitis (EC) is a type of EGID.
- Corticosteroids are the standard first-line treatment for EC refractory to dietary interventions.
Observation:
- An 8-month-old infant presented with persistent bloody diarrhea, anemia, and failure to thrive (FTT) since birth.
- Dietary therapy and initial investigations were unsuccessful.
- Diagnosis of EC was confirmed via rectal biopsies at 5 months of age.
Findings:
- The infant exhibited steroid-resistant EC despite oral prednisolone treatment.
- Combined therapy with montelukast and ketotifen led to significant improvement in diarrhea and weight gain.
- The patient remained symptom-free with normal growth during a 5-year follow-up after treatment cessation.
Implications:
- Montelukast and ketotifen represent a potential therapeutic option for steroid-resistant EC in infants.
- This combination therapy may offer an alternative for managing refractory eosinophilic colitis.
- Further research is warranted to explore the efficacy and safety of this combined treatment approach.
Abstract:
Eosinophilic colitis (EC) belongs to a group of idiopathic diseases called eosinophilic gastrointestinal disorders, which are characterized by eosinophil-predominant inflammation in the gastrointestinal tract. Corticosteroids is the first-line pharmacotherapy for EC refractory to diet therapy. We report an infant with steroid-resistant EC, who successfully returned to a healthy growth trajectory under the combined therapy of montelukast and ketotifen. An 8-month-old boy presented with bloody diarrhea, anemia, and failure to thrive (FTT) that started 6 days after birth. The patient has no known allergies. A trial of elementary diet was unsuccessful. The results of several stool cultures were unremarkable. Similarly, lower gastrointestinal series failed to identify anything significant. At 3 months of age, an esophagogastroduodenoscopy with biopsies from the distal duodenum and proximal jejunum were unremarkable. The diarrhea and FTT persisted. A rectosigmoidoscopy with biopsies was performed; the results led to the diagnosis of EC at 5 months of age. Oral prednisolone 1 mg/kg/day was prescribed; however, 3 months into the treatment, persistent bloody diarrhea and FTT were still noted. Montelukast and ketotifen were added, after which diarrhea and weight gain started to improve. Prednisolone and montelukast/ketotifen were tapered off 6 months after. He remains symptom free and has normal growth and development in a 5-year follow-up.
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