Bullous pemphigoid in infancy: Clinical and epidemiologic characteristics

Orith Waisbourd-Zinman1, Dani Ben-Amitai, Arnon D Cohen

  • 1Pediatric Dermatology Unit, Schneider Children's Medical Center of Israel, Petah-Tiqva, Israel.

Insights

Infantile bullous pemphigoid (BP) is not as rare as previously thought, with distinct lesion distribution patterns compared to childhood BP. Laboratory results, treatment, and prognosis show no significant differences.

Area of Science:

  • Dermatology
  • Pediatrics
  • Immunology

Background:

  • Bullous pemphigoid (BP) is an autoimmune blistering disease.
  • Recent cases suggest an increase in infantile BP, necessitating further investigation.

Observation:

  • A retrospective review of infantile BP cases in Israel (2004-2006) and a literature search were conducted.
  • The study compared clinical and laboratory features of infantile BP with childhood BP.

Findings:

  • Infantile BP incidence in Israel was 2.36:100,000/year.
  • Acral involvement was significantly higher in infantile BP (79%) versus childhood BP (17%).
  • Genital involvement was rare in infantile BP (5%) compared to childhood BP (44%).
  • IgM deposition at the dermoepidermal junction was more frequent in childhood BP (29%) than infantile BP (10%).

Implications:

  • Infantile BP may be underdiagnosed.
  • Age-related differences in BP lesion distribution exist.
  • No major differences in laboratory findings, treatment, or prognosis were observed between infantile and childhood BP.
Abstract

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