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Palmar and plantar lichen planus: a case report and review of theliterature

机译:手掌和足底扁平苔藓:一例报告并复习文献

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摘要

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.
机译:掌plant扁平苔藓是一种罕见的皮肤病。我们提出了一例38岁的白人男性,右脚底足有瘙痒,鳞状病变。体格检查发现斑块呈白色,多刺性角化丘疹丘疹和局灶性鳞屑。活检显示表皮角化过度和棘皮症。免疫组织化学染色显示表皮和/或类苔质内有CD3,CD8,CD45,CD68,髓样组织抗原,BCL2,p27,p53,HLA-DPDQDR,金属硫蛋白和金属蛋白酶组织抑制剂浸润阳性。1.确诊为PPLP ;该病例说明PPLP在鉴别具有明显交界性炎症成分的不常见足部皮肤病时应予以考虑。

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