Pellagra in a child--a rare entity
Kikkeri Narayanashetty Naveen1, Varadraj V Pai, Praveen Bagalkot
1Department of Dermotology, Sri Dharmasthala Manjunatheshwara College of Medical Sciences and Hospital.
Pellagra, a niacin deficiency disease, is rare in children. This case highlights rapid skin lesion resolution in an 11-year-old girl treated with Nicotinamide (vitamin B3).
Area of Science:
- Pediatrics
- Dermatology
- Nutritional Science
Background:
- Pellagra, a condition resulting from niacin deficiency, is uncommon in pediatric populations.
- While typically associated with alcoholism or malabsorption syndromes, pediatric pellagra is exceptionally rare.
- This case focuses on a unique presentation of pellagra in a child.
Observation:
- An 11-year-old girl presented with distinct, symmetrical skin lesions.
- Lesions were characterized as hyperpigmented, hyperkeratotic, thick, and scaly plaques with surrounding erythema.
- Affected areas included the hands, arms, feet, legs, and neck sides.
Findings:
- The patient received a therapeutic dose of 100 mg of Nicotinamide.
- Rapid and complete resolution of the characteristic skin lesions was observed post-treatment.
- The child's overall condition improved significantly following nicotinamide administration.
Implications:
- This case underscores the importance of considering nutritional deficiencies, such as niacin deficiency, in pediatric dermatological presentations.
- Early diagnosis and treatment with Nicotinamide can lead to rapid and effective recovery in pediatric pellagra.
- Highlights the successful management of a rare childhood condition through targeted nutritional supplementation.
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