Abstract |
Palmoplantar lichen planus is an uncommon dermatosis. We present a case of 38-year-old Caucasian male with a history of pruritic, scaly lesions on the right plantar foot. Physical examination revealed whitish plaques and numerous spiny hyperkeratotic papules and focal scaling. A biopsy demonstrated orthohyperkeratosis and acanthosis of the epidermis. Immunohistochemical staining revealed positivity within the epidermis and/or lichenoid infiltrate with CD3, CD8, CD45, CD68, myeloid histiod antigen, BCL2, p27, p53, HLA-DPDQDR, metallothionein and tissue inhibitor of metalloproteinases 1. The diagnosis of PPLP was thus confirmed; this case illustrates that PPLP should be considered in the differential diagnosis of uncommon foot dermatoses with a significant junctional inflammatory component.
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Authors | Ana Maria Abreu Velez, Michael S Howard, Neville Pereyo |
Journal | Anais brasileiros de dermatologia
(An Bras Dermatol)
2015 May-Jun
Vol. 90
Issue 3 Suppl 1
Pg. 175-7
ISSN: 1806-4841 [Electronic] Spain |
PMID | 26312708
(Publication Type: Case Reports, Journal Article, Review)
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Topics |
- Adult
- Biopsy
- Diagnosis, Differential
- Epidermis
(pathology)
- Foot Dermatoses
(pathology)
- Hand Dermatoses
(pathology)
- Humans
- Immunohistochemistry
- Lichen Planus
(pathology)
- Male
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