European Journal of Dermatology
MENUPorokeratosis and immunosuppression Volume 8, numéro 7, October - November 1998
Illustrations
Department of Dermatology, Ed. Herriot Hospital, 69437 Lyon Cedex 03, France.
- Page(s) : 459-65
- Année de parution : 1998
The term "porokeratosis" (PK) encompasses a group of uncommon hereditary or acquired diseases of keratinization of unknown aetiology, presenting with varying clinical aspects but sharing a common histopathological aspect, characterised by the presence of the "cornoid lamella". PK was first described by Mibelli in 1893 [1]; several other clinical forms were subsequently identified. PK may appear in otherwise healthy persons but may also [...]