Related Experiment Video
Updated: May 20, 2026

Technique of Conjunctival Biopsy and Direct Immunofluorescence for Diagnosing Mucous Membrane Pemphigoid
Published on: June 17, 2025
Pediatric pemphigus vulgaris: durable treatment responses achieved with prednisone and mycophenolate mofetil (MMF)
Andrea Baratta1, Diana Camarillo, Christine Papa
1Department of Dermatology, St. John's Episcopal Hospital, Far Rockaway, New York, USA.
Abstract:
Pemphigus vulgaris (PV) is a chronic autoimmune blistering disease of the skin and mucous membranes. Most cases occur in adults; cases in children are rare. This report describes the clinical presentations and treatment responses of three children with PV, as confirmed according to histology and indirect immunofluorescence studies. In all three cases, oral prednisone used in conjunction with mycophenolate mofetil (MMF) resulted in complete clinical remission, during which all pharmacotherapy was successfully discontinued. Resolution of the skin and mucosal blistering tended to occur quickly with prednisone, and after initiation of treatment with MMF, discontinuation of all pharmacotherapy was achieved within a range of 10 to 30 months in the three patients. One patient experienced a recurrence of genital lesions 19 months after discontinuation of therapy, but the condition remitted within 2 weeks with topical corticosteroid therapy. At the time of this report, the duration of complete remission ranged from 6 to 19 months. In summary, combination therapy with prednisone and MMF for pediatric PV appears to be a safe and effective approach that is associated with durable remission.
Insights
Pemphigus vulgaris (PV) in children is rare. Combination therapy with prednisone and mycophenolate mofetil (MMF) achieved durable remission in three pediatric cases, allowing for treatment discontinuation.
Area of Science:
- Dermatology
- Autoimmune Diseases
- Pediatric Medicine
Background:
- Pemphigus vulgaris (PV) is a rare, chronic autoimmune blistering disease affecting skin and mucous membranes, predominantly in adults.
- Pediatric cases of PV are uncommon, necessitating research into effective treatment strategies for this demographic.
Observation:
- This study reports on three children diagnosed with PV via histology and immunofluorescence.
- Clinical presentations and responses to a specific treatment regimen were documented.
Findings:
- Combination therapy using oral prednisone and mycophenolate mofetil (MMF) led to complete clinical remission in all three pediatric patients.
- Pharmacotherapy was successfully discontinued in all cases within 10 to 30 months.
- One patient experienced a recurrence, successfully treated with topical corticosteroids.
Implications:
- Combined prednisone and MMF therapy presents a safe and effective treatment for pediatric PV.
- This approach is associated with sustained remission, offering a promising therapeutic option for children with this condition.