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Pediatric Collagenous Gastroenterocolitis Successfully Treated with Methotrexate
Beate C Beinvogl1, Jeffrey D Goldsmith2, Ramalingam Arumugam3
1Division of Gastroenterology, Boston Children's Hospital, Boston, MA, USA.
Insights
A pediatric patient with collagenous gastroenterocolitis experienced symptom recurrence after medication withdrawal. Treatment with immunosuppressants and corticosteroids led to sustained remission, highlighting therapeutic options for this rare condition.
Area of Science:
- Gastroenterology
- Pediatric Gastroenterology
- Immunology
Background:
- Collagenous gastroenterocolitis is a rare inflammatory bowel disease characterized by a collagen layer deposition in the colon.
- It often presents with chronic watery diarrhea, malabsorption, and failure to thrive, particularly in pediatric populations.
Observation:
- A previously healthy two-and-a-half-year-old female presented with prolonged watery diarrhea, emesis, and fevers, leading to severe hypoalbuminemia and hypogammaglobulinemia.
- Endoscopic and colonoscopic biopsies confirmed collagenous gastroenterocolitis, necessitating parenteral nutrition due to persistent symptoms.
Findings:
- The patient initially responded to prednisone but relapsed upon transitioning to budesonide.
- Intravenous prednisone followed by intramuscular methotrexate induced a 15-month remission.
- Recurrence of collagenous colitis after methotrexate cessation responded well to a short course of oral budesonide, achieving sustained remission.
Implications:
- This case highlights the potential efficacy of combined immunosuppressive and corticosteroid therapy in managing refractory pediatric collagenous gastroenterocolitis.
- The findings suggest a potential role for methotrexate in long-term maintenance therapy for this condition.
- Successful budesonide retreatment indicates its utility in managing relapses, even after prior treatment failures.
Abstract:
A two-and-one-half-year-old previously healthy female presented with a ten-week history of watery diarrhea, nonbilious and nonbloody emesis, and low-grade fevers. She was found to have severe hypoalbuminemia and hypogammaglobulinemia. Her symptoms persisted, and she became dependent on parenteral nutrition. Biopsies obtained during subsequent endoscopic and colonoscopic studies revealed findings consistent with collagenous gastroenterocolitis. She responded to an empiric course of prednisone, but her symptoms recurred shortly after transitioning to oral budesonide. After successful reinduction with intravenous prednisone, intramuscular methotrexate was initiated. She remained asymptomatic during a 15-month course of therapy, and she continued to do well clinically until approximately nine months after weaning off methotrexate. At that point, she experienced a recurrence of diarrhea, and repeat endoscopic evaluation confirmed collagenous colitis. This responded nicely to a short course of oral budesonide, and she has since remained asymptomatic and off any therapy.
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