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Lichen Planus Pigmentosus: The Controversial Consensus
Aparajita Ghosh1, Arijit Coondoo1
1Department of Dermatology, KPC Medical College and Hospital, Kolkata, West Bengal, India.
Indian Journal of Dermatology
|October 1, 2016
Summary
Lichen planus pigmentosus (LPP) is a skin condition causing dark patches, primarily on sun-exposed areas, especially in darker skin tones. Its exact relationship to erythema dyschromicum perstans remains debated among dermatologists.
Area of Science:
- Dermatology
- Pathology
Background:
- Lichen planus pigmentosus (LPP) is a pigmented variant of lichen planus first described in India.
- LPP predominantly affects individuals with darker skin tones and presents with insidious onset of hyperpigmented macules and patches.
Purpose of the Study:
- To describe the clinical and histopathological features of lichen planus pigmentosus.
- To discuss the differential diagnosis and controversial identity of LPP with erythema dyschromicum perstans.
- To report associated conditions and variants of LPP.
Main Methods:
- Clinical observation and histopathological examination of affected skin.
- Review of existing literature on LPP and related conditions.
Main Results:
- LPP typically manifests on sun-exposed areas, sparing palms, soles, and nails.
- Histopathology reveals epidermal atrophy, basal cell vacuolar degeneration, and dermal pigment incontinence.
- Significant histopathological similarities exist between LPP and erythema dyschromicum perstans, though clinical and immunological differences are noted.
Conclusions:
- LPP is a distinct entity, despite histopathological similarities with erythema dyschromicum perstans.
- Associations with Hepatitis C virus, frontal fibrosing alopecia, Bazex acrokeratosis, and nephrotic syndrome have been reported.
- A rare variant, LPP inversus, affects covered areas and predominantly white-skinned individuals.
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