Pityriasis rubra pilaris (PRP) is an idiopathic, papulosquamous inflammatory dermatosis. It is
characterized by hyperkeratotic follicular papules coalescing into orange-red scaly plaques …

Pityriasis rubra pilaris (PRP) is a rare inflammatory skin disease that affects men and women
of all ages and also children. The clinical appearance of PRP is highly variable, as is the …

Background Heterozygous mutations in caspase recruitment domain family member 14
gene (CARD14) have been shown to be associated with psoriasis and familial pityriasis …

Pityriasis rubra pilaris (PRP) ist eine seltene papulosquamöse Erkrankung. Die Behandlung
ist schwierig; das therapeutische Arsenal umfasst topische Corticosteroide, Phototherapie …

Importance Pityriasis rubra pilaris (PRP) is a rare papulosquamous disorder with limited
epidemiologic and clinicopathologic data. Little information is available on long-term …

Pityriasis rubra pilaris (PRP) is a rare inflammatory papulosquamous skin disease that is
often refractory to conventional therapies. The off-label use of biologics, such as anti–tumor …

Importance Pityriasis rubra pilaris is a rare and disabling cutaneous disease that is
frequently recalcitrant to conventional therapies and appears to involve interleukin (IL)-17 …

M. chelonae, M. fortuitum or M. peregrinum arising in patients with diabetes using insulin
pen devices or syringe and needles have been reported. 8, 9 Identification of …

Pityriasis rubra pilaris (PRP) represents a group of rare chronic inflammatory skin disorders
in which around one in 20 affected individuals show autosomal dominant inheritance. In …

Abstract Interleukin (IL)-23 is an important regulator of T helper-17 lymphocytes, which
influence the cutaneous immune system by production of IL-17 and several other …