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Transient gastro-intestinal disorders during infancy and early childhood. A follow-up study with special reference to

Insights

Many children with coeliac disease (CD) were identified through intestinal biopsy, even with minimal symptoms. This highlights the need for biopsies in those with a history of infant gastro-intestinal issues.

Area of Science:

  • Pediatric Gastroenterology
  • Immunology
  • Gastroenterology

Background:

  • Coeliac disease (CD) diagnosis can be challenging in children, especially those lost to follow-up or initially misdiagnosed.
  • A significant number of pediatric patients with a history of gastro-intestinal symptoms may remain undiagnosed.

Purpose of the Study:

  • To re-evaluate children and adolescents with a history suggestive of coeliac disease.
  • To determine the prevalence of undiagnosed coeliac disease in specific pediatric cohorts.
  • To assess the utility of clinical examination and serological markers versus intestinal biopsy for CD diagnosis.

Main Methods:

  • A reappraisal study involving 38 children and adolescents.
  • Group A: 20 patients with a prior CD diagnosis lost to follow-up.
  • Group B: 18 patients hospitalized for gastro-intestinal symptoms without a CD diagnosis.
  • Clinical examination, Hb, serum IgA, and folate levels were analyzed.
  • Intestinal biopsies were performed for definitive diagnosis.

Main Results:

  • Clinical examinations and serological tests (Hb, IgA, folate) were not effective in identifying coeliac disease cases.
  • Intestinal biopsy revealed coeliac disease in 8 patients (40%) in Group A and 6 patients (33.3%) in Group B.
  • All 14 diagnosed patients had minimal complaints prior to biopsy.
  • The prevalence of CD was similar in both groups.

Conclusions:

  • Intestinal biopsy is crucial for diagnosing coeliac disease, particularly in children with a history of infant malabsorption-related symptoms.
  • Liberal indications for intestinal biopsy should be considered in this patient population.
  • Many undiagnosed coeliac disease cases can be identified through this approach.

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