Pityriasis rubra pilaris (Q43925): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed label, description and/or aliases in pt-br, en |
||
| description / pt-br | description / pt-br | ||
Pitiríase rubra pilar (PRP) é o nome dado a um grupo de dermatoses papuloescamosas clinicamente semelhantes de etiologia desconhecida. Apresentam-se inicialmente com pápulas perifoliculares hiperceratóticas eritematosas, que tendem a coalescer em placas, mas que podem progredir para eritrodermia, particularmente em adultos. A distribuição, idade de início e velocidade de início diferem marcadamente entre pacientes e essas diferenças têm sido usadas para classificar o PRP em numerosos subtipos clinicamente distintos. | |||
| description / en | description / en | ||
Pityriasis rubra pilaris (PRP) is the name given to a group of clinically similar papulosquamous dermatoses of unknown aetiology. They initially present with erythematous, hyperkeratotic perifollicular papules, which tend to coalesce into plaques, but may progress to erythroderma, particularly in adults. The distribution, age of onset and speed of onset differ markedly between patients and these differences have been used to classify PRP into a number of clinically distinct subtypes. | |||
Revision as of 11:09, 13 August 2026
Pityriasis rubra pilaris (PRP) is the name given to a group of clinically similar papulosquamous dermatoses of unknown aetiology. They initially present with erythematous, hyperkeratotic perifollicular papules, which tend to coalesce into plaques, but may progress to erythroderma, particularly in adults. The distribution, age of onset and speed of onset differ markedly between patients and these differences have been used to classify PRP into a number of clinically distinct subtypes.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | EA94 |
||
| English | Pityriasis rubra pilaris |
Pityriasis rubra pilaris (PRP) is the name given to a group of clinically similar papulosquamous dermatoses of unknown aetiology. They initially present with erythematous, hyperkeratotic perifollicular papules, which tend to coalesce into plaques, but may progress to erythroderma, particularly in adults. The distribution, age of onset and speed of onset differ markedly between patients and these differences have been used to classify PRP into a number of clinically distinct subtypes. |
