Pityriasis rubra pilaris (PRP) is a heterogeneous group of rare papulosquamous disorders characterized by folliculocentric keratinization.1 PRP has a bimodal incidence with equal gender predilection.1 It can be spontaneous in nature and associated with familial inheritance or as a paraneoplastic phenomenon.1,2 PRP has a variable clinical presentation with Griffiths criteria classifying PRP into 5 subtypes based on age of onset, clinical course, and prognosis.1 HIV-related PRP and paraneoplastic PRP have been proposed as additional subtypes.
Medicine by Alexandros G. Sfakianakis,Anapafseos 5 Agios Nikolaos 72100 Crete Greece,00306932607174,00302841026182,alsfakia@gmail.com
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Τετάρτη 23 Μαΐου 2018
Secukinumab in pityriasis rubra pilaris: A case series demonstrating variable response and the need for minimal clinical datasets
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