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Article
June 1989

Porokeratosis Punctata Palmaris et PlantarisA New Entity?

Author Affiliations

From the Departments of Dermatology (Dr Lestringant) and Histopathology (Dr Berge), Al-Hada Military Hospital, Taif, Kingdom of Saudi Arabia. Dr Lestringant is presently with the Tawam Hospital, Abu Dhabi, United Arab Emirates.

Arch Dermatol. 1989;125(6):816-819. doi:10.1001/archderm.1989.01670180088013
Abstract

• Seven members from three generations of a Saudi family presented with porokeratosis punctata palmaris et plantaris (PPPP). In our series of patients, the disorder began in their early 20s, seemed to be transmitted as a dominant trait, and affected males only. The elementary lesion was a tiny keratotic spine, and the involvement was strictly limited to the volar aspects of the hands and to the soles of the feet. Histological studies showed a columnar parakeratosis that resembled the cornoid lamella of porokeratosis, but other clinical and histological traits tended to make PPPP an entity that was distinct from true porokeratosis. There have been only six reports in the literature on genuine PPPP before this series.

(Arch Dermatol. 1989;125:816-819)

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