Results 41 to 50 of about 6,111 (249)

Kaposi's Varicelliform Eruption After Treatment With Ixekizumab in a Patient With Pityriasis Rubra Pilaris. [PDF]

Cureus, 2023
Pityriasis rubra pilaris (PRP) is a rare condition characterized by red-orange plaques with islands of sparing with follicular and palmoplantar hyperkeratosis.
Guenther JS, Ahronowitz I, Worswick S.
europepmc   +2 more sources

Acral pityriasis rubra pilaris [PDF]

Canadian Medical Association Journal, 2020
A previously healthy 34-year-old woman presented to her family physician with an asymptomatic erythematous rash on her hands that had been present for several weeks. She had elevated levels of alanine transaminase, alkaline phosphatase and γ-glutamyltransferase, compatible with a diagnosis ...
Michael, Sander, Megan, Sander
openaire   +2 more sources

Loss-of-function mutations in Keratin 32 gene disrupt skin immune homeostasis in pityriasis rubra pilaris. [PDF]

Nat Commun
Pityriasis rubra pilaris (PRP) is an inflammatory papulosquamous dermatosis, characterized by hyperkeratotic follicular papules and erythematous desquamative plaques. The precise pathogenic mechanism underlying PRP remains incompletely understood. Herein,
Shi P, Chen W, Lyu X, Wang Z, Li W, Jia F, Zheng C, Liu T, Wang C, Zhang Y, Mi Z, Sun Y, Chen X, Chen S, Zhou G, Liu Y, Lin Y, Bai F, Sun Q, Ogese MO, Yu Q, Liu J, Liu H, Zhang F.   +23 more
europepmc   +2 more sources

Pityriasis rubra pilaris induced by topical use of imiquimod 5. [PDF]

An Bras Dermatol, 2023
Armillas-Lliteras L, Iglesias-Sancho M, Altemir A, Moreno Romero JA.   +3 more
europepmc   +2 more sources

Late onset pityriasis rubra pilaris type IV treated with low-dose acitretin [PDF]

, 2016
Pityriasis rubra pilaris is a chronic inflammatory dermatosis of unknown etiology and great clinical variability. It has been divided into six categories.
Carvalho, S., Mota, F., Sanches, M., Selores, M.   +3 more
core   +1 more source

Pityriasis rubra pilaris

Dermatology Online Journal, 2003
Pityriasis rubra pilaris is a chronic, papulosquamous dermatosis of unclear etiology. The case of a 61-year-old man with pityriasis rubra pilaris is presented. The clinical forms, histopathologic features, and treatment options of pityriasis rubra pilaris are reviewed.
N. Cammarota, J. Hergocova, T. M. Lotti
  +7 more sources

Pityriasis rubra pilaris – erütrodermia haruldane põhjus. Haigusjuhu kirjeldus [PDF]

, 2017
Eütrodermia on äge dermatoloogiline seisund, mille korral esineb nahal generaliseerunud erüteem, mis haarab 85–90% kehapinnast ning millega kaasneb sageli ketendus.
Erm, Triin, Karelson, Maire, Lepasaar, Alina   +2 more
core   +2 more sources

A Rare Post-infectious Rash: Pityriasis Rubra Pilaris After COVID-19 Infection. [PDF]

Cureus, 2023
Pityriasis rubra pilaris (PRP) is a rare papulosquamous skin disorder that often presents with erythematous follicular-based hyperkeratotic papules that can become confluent and lead to erythroderma and electrolyte and thermoregulatory imbalances ...
Duncan P, Flood D, Dietz C.
europepmc   +2 more sources

Analysis of CARD14 Polymorphisms in Pityriasis Rubra Pilaris: Activation of NF-κB. [PDF]

, 2015
Pityriasis rubra pilaris (PRP) is a rare inflammatory papulo-squamous disorder manifesting with palmoplantar keratoderma and follicular hyperkeratotic papules which tend to coalesce into large, scaly, erythematous plaques often progressing to exfoliative
Andrews, Jonathan, Fuchs-Telem, Dana, Jin Chung, Hye, Keller, Matthew, Kingman, Joshua, Li, Qiaoli, Ross, Nicholas, Sarig, Ofer, Sprecher, Eli, Uitto, Jouni   +9 more
core   +2 more sources

Beneficial effect of ustekinumab in familial pityriasis rubra pilaris with a new missense mutation in CARD14 [PDF]

, 2018
Pityriasis rubra pilaris (PRP) represents a group of rare chronic inflammatory skin disorders in which ~1 in 20 affected individuals show autosomal dominant inheritance.
Hsu, C-K, Levell, N J, Lwin, S M, McGrath, J A   +3 more
core   +1 more source