Bullous pemphigoid (Q43782): 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 | ||
Penfigoide bolhoso é a doença bolhosa autoimune mais comum no mundo ocidental. Afeta principalmente os idosos e tipicamente se apresenta com um eritema urticado pruriginoso que evolui para uma erupção generalizada de bolhas tensas intactas. Às vezes pode envolver mucosas. É caracterizada por anticorpos IgG contra a zona da membrana basal, levando a fendas subepidérmicas que se manifestam clinicamente como bolhas. | |||
| description / en | description / en | ||
Bullous pemphigoid is the most common autoimmune blistering disease in the Western world. It chiefly affects the elderly and typically presents with a pruritic urticated erythema which evolves into a widespread eruption of intact tense blisters. It can sometimes involve mucous membranes. It is characterised by IgG antibodies to the basement membrane zone, leading to subepidermal clefts that are clinically manifest as blisters. | |||
Revision as of 10:55, 13 August 2026
Bullous pemphigoid is the most common autoimmune blistering disease in the Western world. It chiefly affects the elderly and typically presents with a pruritic urticated erythema which evolves into a widespread eruption of intact tense blisters. It can sometimes involve mucous membranes. It is characterised by IgG antibodies to the basement membrane zone, leading to subepidermal clefts that are clinically manifest as blisters.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | EB41.0 |
||
| English | Bullous pemphigoid |
Bullous pemphigoid is the most common autoimmune blistering disease in the Western world. It chiefly affects the elderly and typically presents with a pruritic urticated erythema which evolves into a widespread eruption of intact tense blisters. It can sometimes involve mucous membranes. It is characterised by IgG antibodies to the basement membrane zone, leading to subepidermal clefts that are clinically manifest as blisters. |
