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Published on: October 12, 2012
[Juveline xanthogranuloma. A case report]
Insights
This case study presents juvenile xanthogranuloma (JXG), a rare skin condition in infants. Histopathology confirmed JXG with lipid-rich cells, indicating a benign inflammatory process.
Area of Science:
- Dermatology
- Pediatric Pathology
Background:
- Juvenile xanthogranuloma (JXG) is a common, benign, self-limiting xanthoma typically presenting in infants and young children.
- While often presenting as solitary or multiple cutaneous nodules, JXG can rarely manifest in extracutaneous sites.
Observation:
- A six-month-old boy presented with 17 yellowish, pea-sized papules on his scalp, trunk, and limbs.
- The child was in good health, with only cutaneous lesions observed.
- No other significant laboratory abnormalities were detected.
Findings:
- Histopathology revealed a dense dermal infiltrate composed primarily of histiocytes.
- Foreign-body type giant cells were also present in the dermal infiltrate.
- Sudan III staining identified small lipid droplets within some histiocytes, consistent with xanthogranuloma.
Implications:
- This case highlights the papular presentation of juvenile xanthogranuloma (JXG) in infants.
- The findings support JXG as a benign, lipid-laden histiocytic infiltrate.
- Early diagnosis through histopathology aids in appropriate management and reassurance for affected families.
Abstract:
A case of xanthogranuloma juvenile (the small papular form) in a six month-old boy is presented. Only cutanous lesions are seen and the child is of good health. On the scalp, trunk and limbs there are 17 yellowish pea-sized papules. Histopathology reveals a dense infiltrate in the dermis which is composed of histiocytes, a number of giant cells of the foreign-body type is also present. With Sudan III staining in some of the histiocytes small droplets of lipids are seen. Other laboratory investigations are within normal limits.
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