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Updated: Jun 1, 2026

12:23
Granulocyte-dependent Autoantibody-induced Skin Blistering
Published on: October 12, 2012
[Infantile bullous pemphigoid developing after hexavalent, meningococcal and pneumococcal vaccinations]
M Valdivielso-Ramos1, D Velázquez, A Tortoledo
1Servicio de Dermatología, Servicios de Anatomía Patológica, Hospital Infanta Leonor, Madrid, España. mvaldira@yahoo.es
Anales De Pediatria (Barcelona, Spain : 2003)
|June 17, 2011
Summary
Bullous pemphigoid, a rare autoimmune blistering disease in children, can be triggered by vaccinations. Early diagnosis and treatment with corticosteroids led to remission in an infant case.
Area of Science:
- Pediatric Dermatology
- Autoimmune Disorders
- Vaccinology
Background:
- Bullous pemphigoid (BP) is an acquired autoimmune blistering disease.
- It is characterized by IgG antibodies targeting the epidermal basement membrane zone.
- BP is exceptionally rare in pediatric populations.
Observation:
- A 3-month-old infant presented with blistering on palms/soles and urticarial plaques.
- The eruption appeared 3 weeks post-vaccination (hepatitis B, DTaP, IPV, Hib, MenC, PCV).
- Symptoms exacerbated following subsequent vaccinations at 4 and 6 months.
Findings:
- The infant was treated with oral deflazacort (1 mg/kg/day).
- Lesion control was achieved within 3 months of continuous therapy.
- The patient remained in remission for 8 months post-treatment.
Implications:
- This case suggests a potential link between vaccinations and bullous pemphigoid onset in infants.
- While the exact mechanism remains unclear, temporal association warrants further investigation.
- Prompt diagnosis and corticosteroid therapy are crucial for managing pediatric bullous pemphigoid.
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