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Published on: September 20, 2018
Childhood granulomatous periorificial dermatitis in children with extra-facial involvement
Rameshwar Gutte1, Sarika Holmukhe, Gaurav Garg
1Department of Dermatology, Seth GS Medical College and King Edward Memorial Hospital, Mumbai, India.
Insights
Childhood granulomatous periorificial dermatitis (CGPD) is a recognized skin condition. This case highlights CGPD in a child with juvenile rheumatoid arthritis (JRA), showing facial and extra-facial lesions.
Area of Science:
- Pediatric Dermatology
- Dermatopathology
Background:
- Childhood granulomatous periorificial dermatitis (CGPD) is a distinct facial rash.
- Juvenile rheumatoid arthritis (JRA) is a chronic inflammatory condition affecting children.
Observation:
- A six-year-old boy with JRA presented with a one-month history of itchy, red, raised, yellowish facial and extra-facial lesions.
- Physical examination revealed erythematous, scaly papules on the face, neck, trunk, and upper extremities, with excoriations.
Findings:
- Skin biopsy confirmed the diagnosis of CGPD.
- The case demonstrated unusual extra-facial involvement of CGPD.
Implications:
- This case expands the understanding of CGPD presentation, particularly in children with autoimmune conditions like JRA.
- Early diagnosis and management are crucial for favorable outcomes, even with extensive skin involvement.
Abstract:
Childhood granulomatous periorificial dermatitis (CGPD) is a self-limiting and well-recognized entity. A six-year-old male child, a known case of juvenile rheumatoid arthritis (JRA) presented with multiple red raised and yellowish lesions over the face, neck, trunk and upper extremities since one month with occasional itching. Cutaneous examination revealed multiple erythematous scaly papules of size up to 5 mm around the mouth, nose and periorbital areas, neck, trunk and upper extremities with few excoriations. Lesional skin biopsy was pathognomic of CGPD. We report a six-year-old Indian male child with extra-facial involvement and healing with small atrophic pigmented scars in a known case of JRA.
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