Acute onset of blisters in an infant with acrodermatitis enteropathica: A case report

Kristyna Cleminson1, Peter R Hull1, Emma Price1

  • 1Department of Dermatology, Dalhousie University, Halifax, NS, Canada.

Insights

Acrodermatitis enteropathica, a congenital zinc malabsorption disorder, can present with acute infant blisters. Early diagnosis and lifelong zinc supplementation are crucial for managing this rare but treatable condition.

Area of Science:

  • Pediatric Dermatology
  • Nutritional Disorders
  • Genetic Diseases

Background:

  • Acrodermatitis enteropathica (AE) is a rare autosomal recessive disorder caused by impaired zinc absorption.
  • It typically manifests in early infancy, often after breastfeeding cessation.
  • Cutaneous symptoms are characteristic but can vary in presentation.

Observation:

  • This report details a pediatric case of AE presenting with acute-onset blistering in infancy.
  • Blisters, while a known feature, are not always prominent and may be overlooked.
  • The case highlights the importance of considering AE in the differential diagnosis of acute blistering disorders in infants.

Findings:

  • Acrodermatitis enteropathica can present with acute blistering, mimicking other infantile dermatoses.
  • A comprehensive differential diagnosis for infantile blistering is essential for timely recognition.
  • Lifelong zinc supplementation is the cornerstone of AE management.

Implications:

  • Increased awareness of AE's varied cutaneous presentations can improve diagnostic accuracy.
  • Prompt identification and treatment of AE prevent severe morbidity associated with zinc deficiency.
  • This case underscores the critical role of pediatricians and dermatologists in recognizing and managing genetic malabsorption syndromes.

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