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Updated: Sep 22, 2026

Granulocyte-dependent Autoantibody-induced Skin Blistering
Published on: October 12, 2012
Pemphigus in children
1Department of Dermatology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Insights
This study reports on seven boys with pemphigus, a rare autoimmune blistering disease. All patients experienced an excellent prognosis following treatment with corticosteroids.
Area of Science:
- Dermatology
- Autoimmune Diseases
- Pediatrics
Background:
- Pemphigus is a group of rare autoimmune blistering diseases.
- Pemphigus vulgaris and pemphigus foliaceus are the most common subtypes.
- Pediatric autoimmune blistering diseases are uncommon, with limited case reports.
Observation:
- This report details seven male pediatric patients diagnosed with pemphigus.
- The youngest patient presented with disease onset at age seven.
- Six boys had pemphigus vulgaris, and one boy had pemphigus foliaceus.
Findings:
- Three patients with pemphigus vulgaris received intravenous dexamethasone pulse therapy.
- The remaining four patients were treated with oral corticosteroid therapy.
- All seven pediatric patients achieved an excellent prognosis, indicating successful disease management.
Implications:
- Corticosteroid therapy, both intravenous and oral, appears effective in managing pediatric pemphigus.
- Early diagnosis and prompt treatment are crucial for favorable outcomes in pediatric autoimmune blistering diseases.
- Further research into long-term outcomes and potential side effects of corticosteroid treatment in children is warranted.
Abstract:
Six boys with pemphigus vulgaris and one boy with pemphigus foliaceus are reported. The youngest patient had onset of the disease at the age of 7 years. Three patients with pemphigus vulgaris were treated with intravenous dexamethasone pulses, while the remaining four received oral corticosteroid therapy. The prognosis in all patients was excellent.
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