Results 71 to 80 of about 6,111 (249)

Systemic sclerosis in a patient with pityriasis rubra pilaris [PDF]

, 2011
Pityriasis rubra pilaris (PRP) is a rare, chronic erythematous squamous disorder of unknown etiology. It has been found in association with several autoimmune diseases, including thyroiditis, myositis, myasthenia gravis and vitiligo.
Bahloul, Z, Frigui, M, Frikha, F, Masmoudi, H, Turki, H   +4 more
core   +2 more sources

Pityriasis Rubra Pilaris

, 2015
Pityriasis rubra pilaris (PRP) is a chronic, inflammatory, papulosquamous disorder of keratinization of unknown etiology. It appears both in hereditary and in acquired form. According to the classification by Griffiths, there are six types of PRP: classical adult (type I), atypical adult (type II), classical juvenile (type III), circumscribed juvenile (
Petrov, Andrej, Pljakoska, Vesna
openaire   +2 more sources

Successful treatment of pityriasis rubra pilaris with brodalumab after nonresponse to IL-17A inhibition: A role for the innate cytokine IL-17C. [PDF]

JAAD Case Rep
Valido K, Murphy MJ, Leventhal JS, Damsky W.   +3 more
europepmc   +2 more sources

Dermatology 2.0: Precision medicine for inflammatory skin diseases

Journal of the European Academy of Dermatology and Venereology, EarlyView.
Digital immune mapping of transcriptomics profiles from inflammatory skin disease biopsies enables precise molecular diagnosis, quantification of immune modules and personalized therapy selection by matching dominant immune signatures to targeted treatments.
Jeremy Di Domizio, Antoine Girardin, Curdin Conrad, Teofila Seremet, Michel Gilliet   +4 more
wiley   +1 more source

Folliculotropic Mycosis Fungoides: Update on Diagnosis, Clinicopathological Stage, and Management

Dermatologic Therapy, Volume 2026, Issue 1, 2026.
Folliculotropic mycosis fungoides (FMF) is a rare subtype of MF, characterized by prominent folliculotropism in histopathology. Clinically, FMF exhibits polymorphic presentations, mainly including follicular papules, plaques, alopecia, and other nonspecific lesions, with a predilection for the head and neck region, leading to frequent misdiagnosis ...
Xingyu Li, Jie Liu, Nicola Pimpinelli
wiley   +1 more source

Pityriasis rubra pilaris (Devergie's disease): clinical case [PDF]

Саратовский научно-медицинский журнал, 2016
Pityriasis rubra pilaris (Devergie's disease) is a rare chronic papulosquamous skin disease, it is of unknown etiology, leading to palmoplantar keratoderma, erythroderma and ectropion. Due to its rarity and difficulty in differentiating it with psoriasis,
Galkina ЕМ, Utz SR, BakulevAL, Minyonok ТА.   +3 more
doaj  

Papulosquamous: clinicopathological [PDF]

, 2017
Background: Papulosquamous disorders comprise a group of dermatoses that have distinct morphologic features. The characteristic primary lesion of these disorders is a papule, usually erythematous, that has a variable amount of scaling on the surface ...
Narayankar, Shilpa Laxmikant, Pandit, Gopal Ambadasrao   +1 more
core   +2 more sources

Body image and mental health in chronic skin conditions: A psychosomatic perspective from a systematic review

Applied Psychology: Health and Well-Being, Volume 17, Issue 6, December 2025.
Abstract This systematic review aimed to consolidate evidence regarding the effect of skin diseases (SD) on body image (BI) and to examine the sociodemographic, clinical, and psychosocial correlates of BI in individuals with SD. A comprehensive search was conducted in December 2024 across nine databases, including MEDLINE, Web of Knowledge, PsycINFO ...
Tatiane Fidelis, Filipa M. Vieira, Kylee M. Miller, Sandra Torres   +3 more
wiley   +1 more source

Classical Juvenile Pityriasis Rubra Pilaris Treated With Secukinumab: Case Report and a Review of Biological Treatments in the Pediatric Population

Pediatric Dermatology, Volume 42, Issue 6, Page 1214-1220, November/December 2025.
ABSTRACT Pityriasis rubra pilaris (PRP) is a rare, chronic papulosquamous disorder with limited treatment options in pediatric patients. We report the case of a 9‐year‐old boy with juvenile PRP (type III), who achieved complete disease remission after treatment with secukinumab, an IL‐17A inhibitor, following initial therapeutic resistance to topical ...
Zeno Fratton, Giuseppe Stinco, Enzo Errichetti   +2 more
wiley   +1 more source

Pathogenesis of Pseudocheckerboard Pattern in Mechanic's Hands

The Journal of Dermatology, Volume 52, Issue 9, Page 1418-1423, September 2025.
ABSTRACT Among the relatively common manifestations of dermatomyositis (DM), “mechanic's hands” refer to symmetric hyperkeratotic erythematous lesions on the ulnar aspect of the thumbs and the radial aspect of the index and middle fingers. The “pseudocheckerboard pattern” is a distinct histopathological finding associated with mechanic's hands.
Kyoko Kanno, Mari Kishibe, Masaru Honma, Akemi Ishida‐Yamamoto   +3 more
wiley   +1 more source