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[Acral lichen sclerosus et atrophicus]
M Steff1, A Toulemonde, A Croue
1Service de dermatologie, CHU d'Angers, université d'Angers, 4, rue Larrey, 49933 Angers cedex 9, France.
Annales De Dermatologie Et De Venereologie
|April 1, 2008
Summary
Lichen sclerosus et atrophicus (LS&A) rarely affects only the extremities. This case highlights a unique presentation of LS&A involving the hands, feet, and genital area, expanding the known clinical spectrum of this rare condition.
Area of Science:
- Dermatology
- Pathology
Background:
- Lichen sclerosus et atrophicus (LS&A) is a chronic inflammatory skin condition.
- LS&A typically affects the anogenital region but can present with extragenital manifestations.
- Extremity involvement is uncommon and usually occurs with widespread cutaneous disease.
Observation:
- A 56-year-old woman presented with characteristic ivory white papules on her hands and feet.
- Lesions included keratotic papules on the palms and erythema on the soles.
- Genital and perigenital LS&A was also diagnosed.
Findings:
- Histopathological examination of lesions from both extremities and the genital area confirmed typical features of LS&A.
- This case represents a rare instance of LS&A predominantly affecting the extremities and genital region.
Implications:
- This case expands the recognized clinical presentation of lichen sclerosus et atrophicus.
- It underscores the importance of considering LS&A in cases of isolated extremity or combined extremity-genital skin lesions.
- Further research may elucidate specific triggers or predispositions for this pattern of LS&A.
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