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Updated: May 14, 2026

Granulocyte-dependent Autoantibody-induced Skin Blistering
Published on: October 12, 2012
Infantile bullous pemphigoid refractory to corticosteroids: Response to cyclosporine
Lucía Scillama1, Natalia Mantero1, Laura Caristia1
1Department of Dermatology, Hospital Nacional Prof. Alejandro Posadas, El Palomar, Argentina.
Insights
Bullous pemphigoid, a rare autoimmune skin condition in children, was effectively treated with cyclosporine in a 4-month-old infant. This treatment led to remission within two weeks without adverse effects, offering a new therapeutic option.
Area of Science:
- Dermatology
- Immunology
- Pediatrics
Background:
- Bullous pemphigoid (BP) is a rare autoimmune blistering disease in pediatric patients, typically affecting the elderly.
- Conventional treatments for pediatric bullous pemphigoid often have significant side effects or limited efficacy.
Abstract:
Bullous pemphigoid is a common autoimmune bullous skin disease in elderly patients, but it is rare in children. We present the case of a 4-month-old boy diagnosed with bullous pemphigoid that was refractory to conventional treatment, who achieved remission after 2 weeks of treatment with cyclosporine without experiencing any adverse effects.
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