Case report: bullous pemphigoid development underlies dystrophic epidermolysis bullosa disease worsening
Autoimmune response to cutaneous basement membrane components superimposed on a genetic skin fragility disease, hereditary epidermolysis bullosa (EB), has been described, but its effects on disease course remain unclear. We report a 69-year-old individual with congenital skin fragility and acral tra...
Main Authors: | Giovanni Di Zenzo, Giovanna Floriddia, Sabrina Rossi, Feliciana Mariotti, Alessia Primerano, Angelo Giuseppe Condorelli, Biagio Didona, Daniele Castiglia |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2022-07-01
|
Series: | Frontiers in Immunology |
Subjects: | |
Online Access: | https://www.frontiersin.org/articles/10.3389/fimmu.2022.929286/full |
Similar Items
-
A <i>COL7A1</i> Variant in a Litter of Neonatal Basset Hounds with Dystrophic Epidermolysis Bullosa
by: Teresa Maria Garcia, et al.
Published: (2020-12-01) -
Case report: Bullous pemphigoid arising in a patient with scleroderma and multiple sclerosis
by: Francesco Moro, et al.
Published: (2022-12-01) -
Diagnostic value of elastic fibers staining in dystrophic epidermolysis bullosa
by: Min-tong HE, et al.
Published: (2020-04-01) -
Dystrophic epidermolysis bullosa: genotype-phenotype correlations
by: Alexey A. Kubanov, et al.
Published: (2023-10-01) -
Immune Disregulation in Cutaneous Squamous Cell Carcinoma of Patients with Recessive Dystrophic Epidermolysis Bullosa: A Single Pilot Study
by: Angela Filoni, et al.
Published: (2022-01-01)