Childhood lichen planus pemphigoides triggered by chickenpox
T S Mohanarao1, Gummalla Ajay Kumar1, Kavya Chennamsetty1
1Department of Dermatology, Venereology and Leprosy, Andhra Medical College, Visakhapatnam, Andhra Pradesh, India.
Indian Dermatology Online Journal
|January 17, 2015
Summary
Lichen planus pemphigoides (LPP) is a rare autoimmune blistering disease. This case study details LPP in a child, likely triggered by varicella, confirmed via biopsy and immunofluorescence.
Area of Science:
- Dermatology
- Autoimmune Blistering Diseases
Background:
- Lichen planus pemphigoides (LPP) is a rare autoimmune bullous disorder.
- It is exceptionally rare in pediatric populations.
Observation:
- A 5-year-old girl presented with clinical features suggestive of LPP.
- The condition was potentially triggered by a preceding varicella infection.
Findings:
- Diagnosis was confirmed through histopathology and direct immunofluorescence.
- Biopsies showed lichen planus characteristics on papules and bullous pemphigoid features on blisters.
- Direct immunofluorescence revealed immunoglobulin G and C3 deposition at the basement membrane zone.
Implications:
- This case highlights the importance of comprehensive diagnostic evaluation for LPP in children.
- Understanding triggers like varicella is crucial for pediatric autoimmune blistering diseases.
- Histopathology and immunofluorescence are key for accurate LPP diagnosis.
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