Pemphigoid nodularis (Q104456): Difference between revisions
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| description / pt-br | description / pt-br | ||
Penfigoide nodular é um subtipo de penfigoide com manifestações de prurigo nodular e do penfigoide bolhoso. Os pacientes apresentam nódulos, pápulas ou placas pruriginosas. As bolhas geralmente são observadas em algum momento durante o curso da doença, mas também podem estar ausentes. A confirmação do diagnóstico é frequentemente desafiadora, mas a imunopatologia é semelhante ao penfigoide bolhoso comum. As pernas são as localizações comumente afetadas, mas a condição pode ser generalizada e difícil de gerenciar. | |||
| description / en | description / en | ||
Pemphigoid nodularis is a subtype of pemphigoid with features of both nodular prurigo and bullous pemphigoid. Patients present with pruritic nodules, papules or plaques. Blisters are usually seen at some point during the course of the disease but may also be absent. Confirming the diagnosis is often challenging but the immunopathology is similar to ordinary bullous pemphigoid. Legs are the commonly affected sites but the condition can be widespread and difficult to manage. | |||
Revision as of 10:18, 17 August 2026
Pemphigoid nodularis is a subtype of pemphigoid with features of both nodular prurigo and bullous pemphigoid. Patients present with pruritic nodules, papules or plaques. Blisters are usually seen at some point during the course of the disease but may also be absent. Confirming the diagnosis is often challenging but the immunopathology is similar to ordinary bullous pemphigoid. Legs are the commonly affected sites but the condition can be widespread and difficult to manage.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_957206549 |
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| English | Pemphigoid nodularis |
Pemphigoid nodularis is a subtype of pemphigoid with features of both nodular prurigo and bullous pemphigoid. Patients present with pruritic nodules, papules or plaques. Blisters are usually seen at some point during the course of the disease but may also be absent. Confirming the diagnosis is often challenging but the immunopathology is similar to ordinary bullous pemphigoid. Legs are the commonly affected sites but the condition can be widespread and difficult to manage. |
