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Granulomatous periorificial dermatitis: a variant of granulomatous rosacea in children?
Chere R Lucas1, Neil J Korman, Anita C Gilliam
1Department of Dermatology, University Hospital of Cleveland/Case Western Reserve University, Cleveland, OH, USA.
Insights
Granulomatous periorificial dermatitis (GPD) is a rare skin condition in children, often misdiagnosed. This case highlights its distinct features and the importance of accurate diagnosis for appropriate management.
Area of Science:
- Dermatology
- Pediatric Dermatology
- Dermatopathology
Background:
- Granulomatous periorificial dermatitis (GPD) is a distinct facial eruption in children.
- It can be misdiagnosed as sarcoidosis, infection, or granulomatous rosacea.
- GPD is also known as facial Afro-Caribbean childhood eruption (FACE).
Observation:
- A 13-year-old Jamaican boy presented with perioral and periocular papules.
- Initial diagnosis was sarcoidosis, treated with oral corticosteroids, with subsequent recurrence.
- Facial papule biopsy revealed dense granulomatous infiltrate with prominent lymphocytes.
Findings:
- Histopathology shows a dense granulomatous infiltrate with surrounding lymphocytes.
- Cultures are consistently negative.
- GPD is histologically similar to granulomatous rosacea, necessitating clinical correlation.
Implications:
- Accurate diagnosis of GPD is crucial to avoid unnecessary treatments.
- Distinguishing GPD from sarcoidosis is important due to the lack of systemic involvement.
- GPD is a self-limited condition, and appropriate diagnosis guides conservative management.
Background:
We report a case of granulomatous periorificial dermatitis (GPD). A 13-year-old Jamaican boy presented with pink to flesh-colored perioral and periocular papules that erupted during a summer visit to Jamaica. The child was initially diagnosed with sarcoidosis and treated with oral corticosteroids, but the eruption recurred 2 years later. He was referred to Dermatology. Biopsy of one of the facial papules revealed a dense granulomatous infiltrate with surrounding prominent lymphocytes. A diagnosis of GPD was made.
Objective And Conclusion:
Also known as facial Afro-Caribbean childhood eruption (FACE), GPD occurs in prepubertal children. It can be confused with sarcoidosis, infection, and granulomatous rosacea but contains lymphocytes around the granulomas and lacks the systemic involvement seen in sarcoidosis. Cultures are invariably negative. The histologic features of GPD and granulomatous rosacea can be identical, and certain treatments may exacerbate the condition, highlighting the importance of clinical correlation. The correct diagnosis is important to minimize treatment as GPD is ultimately self-limited.
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