Results 41 to 50 of about 3,018 (196)
Case for diagnosis. Atypical Grover's disease, [PDF]
Anais Brasileiros de Dermatologia, 2021 A 55-year-old male presented with an eight-month history of erythematous papules and plaques with demarcated areas of spared skin on his trunk, upper extremities, neck, and face.
Pablo Vargas-Mora +3 more
doaj +1 more source
Der Hautarzt, 2012 Pityriasis rubra pilaris is an inflammatory papulosquamous skin disease of unknown etiology. Incidence rates vary between 1:5,000-1:50,000. Six subtypes are differentiated on clinical background. The juvenile circumscribed subtype has best prognosis. Generalized disease impairs quality of life of patients.
Leger, Marie +5 more
openaire +5 more sources
Autoinflammatory keratinization diseases: An emerging concept encompassing various inflammatory keratinization disorders of the skin [PDF]
, 2018 Classifying inflammatory skin diseases is challenging, especially for the expanding group of disorders triggered by genetic factors resulting in hyperactivated innate immunity that result in overlapping patterns of dermal and epidermal inflammation with ...
Akiyama, Masashi +3 more
core +5 more sources
Systemic sclerosis in a patient with pityriasis rubra pilaris [PDF]
The Pan African Medical Journal, 2010 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.
Hamida Turki +4 more
doaj
Psoriasiform pemphigus foliaceus: a report of two cases [PDF]
, 2012 Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/91229/1/j.1600-0560.2012.01866.x ...
Chen +15 more
core +1 more source
Patients with keratinization disorders due to ABCA12 variants showing pityriasis rubra pilaris phenotypes [PDF]
, 2023 Pathogenic variants in ABCA12 are important causative genetic defects for autosomal recessive congenital ichthyoses (ARCI), which include congenital ichthyosiform erythroderma (CIE), harlequin ichthyosis, and lamellar ichthyosis.
Akiyama, Masashi +12 more
core +1 more source
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 +4 more
core +2 more sources
, 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
Association pityriasis rubra pilaire et myasthénie [PDF]
, 2011 Le pityriasis rubra pilaire est un trouble de kératinisation rare dont l’étiopathogénie reste inconnue mais dont l’association avec autres pathologies a été déjà rapportée.
Agharbi, FZ +5 more
core +2 more sources
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 +1 more
core +2 more sources