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Published on: December 1, 2012
One-month-old infant with multiple ulcers of stomach, small bowel, large bowel, and protein-losing enteropathy: case
1Department of Pediatrics, University of Louisville, KY 40202, USA.
Insights
A rare case of infant gastrointestinal ulcers and a mesenteric cyst was successfully treated with immunomodulating drugs. This condition, characterized by severe inflammation and protein loss, resolved with supportive care, showing no relapse in the patient.
Area of Science:
- Pediatric Gastroenterology
- Immunology
- Rare Diseases
Background:
- Multiple inflammatory gastrointestinal ulcers are uncommon in infants.
- Etiologies typically include infections, vasculitis, or autoimmune conditions.
Observation:
- A 1-month-old infant presented with an inflammatory mesenteric cyst and widespread gastrointestinal ulcerations.
- Ulcers were full-thickness, sharply demarcated, and infiltrated by macrophages.
- The infant exhibited protein-losing enteropathy, leading to low serum albumin and IgG.
Findings:
- Treatment involved supportive care and immunomodulating drugs.
- Gastrointestinal inflammation resolved by 3.5 years of age.
- No relapse occurred after medication withdrawal at 5.5 years, though mild hypoalbuminemia and hypogammaglobulinemia persist.
Implications:
- This case presents a unique clinical scenario and successful treatment outcome for infant gastrointestinal ulceration.
- Highlights the potential role of immunomodulatory therapy in severe pediatric inflammatory enteropathies.
- Suggests a possible immune-mediated etiology or a novel presentation of inflammatory bowel disease in infancy.
Abstract:
Multiple inflammatory ulcers of the gastrointestinal tract are rare in young infants. Most cases are caused by infectious organisms, vasculitis, or an autoimmune process. We report a 1-month-old infant who was healthy until he presented with an inflammatory mesenteric cyst, and multiple ulcers of the stomach, duodenum, jejunum, ileum, and colon. Histologically, the ulcerations were sharply demarcated, full thickness, and filled with macrophages. He had a low serum albumin and IgG due to protein-losing enteropathy. He was treated with supportive care and immunomodulating drugs. The gastrointestinal inflammation resolved by 3 and 1/2 years of age. The medications were withdrawn at 5 and 1/2 years of age he had no relapse of clinical symptoms. He continues to have asymptomatic mild hypoalbuminemia and low serum IgG. We could not find a report of a similar clinical presentation and outcome.
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