Intraepithelial autoimmune blistering dermatoses: Clinical features and diagnosis.
IgA pemphigus
IgA/IgG pemphigus
drug-induced pemphigus
fogo selvagem
paraneoplastic autoimmune multiorgan syndrome
paraneoplastic pemphigus
pemphigus erythematosus
pemphigus foliaceus
pemphigus herpetiformis
pemphigus vegetans
pemphigus vulgaris
Journal
Journal of the American Academy of Dermatology
ISSN: 1097-6787
Titre abrégé: J Am Acad Dermatol
Pays: United States
ID NLM: 7907132
Informations de publication
Date de publication:
Jun 2021
Jun 2021
Historique:
received:
03
05
2020
revised:
01
11
2020
accepted:
02
11
2020
pubmed:
9
3
2021
medline:
31
8
2021
entrez:
8
3
2021
Statut:
ppublish
Résumé
Intraepithelial autoimmune blistering dermatoses are a rare group of skin disorders characterized by the intraepithelial disruption of intercellular connections through the action of autoantibodies. The first article in this continuing medical education series explores the background, epidemiology, clinical features, and diagnostic criteria of each of the major intraepithelial autoimmune blistering dermatoses, including pemphigus foliaceus, pemphigus erythematosus, pemphigus herpetiformis, fogo selvagem, pemphigus vulgaris, pemphigus vegetans, drug-induced pemphigus, IgA pemphigus, IgG/IgA pemphigus, and paraneoplastic pemphigus/paraneoplastic autoimmune multiorgan syndrome.
Identifiants
pubmed: 33684498
pii: S0190-9622(21)00471-0
doi: 10.1016/j.jaad.2020.11.075
pii:
doi:
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
1507-1519Informations de copyright
Copyright © 2021 American Academy of Dermatology, Inc. Published by Elsevier Inc. All rights reserved.
Déclaration de conflit d'intérêts
Conflicts of interest None disclosed.