Pityriasis rubra pilaris type V, atypical juvenile (Q96878): Difference between revisions
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Essa forma infantil crônica de pitiríase rubra pilar é incomum e provavelmente geneticamente heterogênea. Pode estar presente ao nascimento ou começar na primeira infância com eritema generalizado e hiperqueratose. A hiperqueratose folicular é uma característica proeminente e a ceratodermia é comum. Alterações semelhantes à esclerodermia foram descritas nas mãos e nos pés. | |||
| description / en | description / en | ||
This chronic childhood form of pityriasis rubra pilaris is uncommon and probably genetically heterogeneous. It may be present at birth or start in early childhood with widespread erythema and hyperkeratosis. Follicular hyperkeratosis is a prominent feature and keratoderma is common. Scleroderma-like changes have been described in the hands and feet. | |||
Revision as of 12:54, 16 August 2026
This chronic childhood form of pityriasis rubra pilaris is uncommon and probably genetically heterogeneous. It may be present at birth or start in early childhood with widespread erythema and hyperkeratosis. Follicular hyperkeratosis is a prominent feature and keratoderma is common. Scleroderma-like changes have been described in the hands and feet.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_178883706 |
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| English | Pityriasis rubra pilaris type V, atypical juvenile |
This chronic childhood form of pityriasis rubra pilaris is uncommon and probably genetically heterogeneous. It may be present at birth or start in early childhood with widespread erythema and hyperkeratosis. Follicular hyperkeratosis is a prominent feature and keratoderma is common. Scleroderma-like changes have been described in the hands and feet. |
