Results 21 to 30 of about 7,109,345 (167)

Real-World Dose Adjustment and Switching of Interleukin-17/23 Inhibitors for Thai Psoriasis. [PDF]

open access: yesDermatol Res Pract
Interleukin (IL)‐17 and IL‐23 inhibitors have transformed psoriasis care, delivering high clearance rates and quality‐of‐life gains. Nevertheless, inadequate response or adverse events can lead to treatment discontinuation or biologic switching. Dose modifications are also commonly implemented in routine practice to optimize efficacy, safety, and cost.
Chaiyabutr C   +6 more
europepmc   +2 more sources

Acrodermatitis continua of Hallopeau and psoriatic arthritis: A case report [PDF]

open access: yes, 2020
A 44-year-old man, previously healthy, consulted for a three-month history of asymmetrical polyarthralgia with inflammatory features involving. small mod large joints.
Arellano Lorca, Javier   +3 more
core   +1 more source

Localized pemphigus vegetans without mucosal involvement

open access: yesIndian Journal of Dermatology, 2014
Pemphigus vegetans is a rare variant of pemphigus vulgaris. A 62-year-old woman presented with erythematous moist vegetative plaque on the left breast and left groin. There was no mucosal involvement.
V K Jain, N Jindal, S Imchen
doaj   +1 more source

Paradoxical pustular psoriasis in a patient with spondyloarthritis treated with secukinumab

open access: yesJEADV Clinical Practice, Volume 2, Issue 4, Page 951-954, December 2023., 2023
Abstract Secukinumab is a monoclonal antibody used to specifically inhibit pathologic interleukin‐17 and therefore effectively manage conditions like plaque psoriasis, psoriatic arthritis and ankylosing spondylitis. Although we know that antitumor necrosis factor molecules can cause paradoxical pustular psoriasis, a few case reports noted this reaction
Daniela Anghel   +4 more
wiley   +1 more source

Pemphigus and pemphigoids: Clinical presentation, diagnosis and therapy

open access: yesJDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 21, Issue 10, Page 1188-1209, October 2023., 2023
Summary Pemphigus and pemphigoid are two potentially life‐threatening groups of autoimmune diseases, characterized by autoantibodies targeting structural components of desmosomes or hemidesmosomes, respectively. Affected patients typically show itchy/painful plaques or blistering skin lesions and/or impairing mucosal blistering and erosions, which may ...
Dario Didona   +3 more
wiley   +1 more source

A Case of Acrodermatitis Continua of Hallopeau Following Chronic Pustular Cheilitis [PDF]

open access: yes, 2016
We describe the case of a young male affected by chronic pustular psoriasis of the lips that remained the only manifestation of acrodermatitis continua of Hallopeau (ACH) for years before the onset of the characteristic hand ...
Marocolo, D   +22 more
core   +1 more source

Epidemiology of generalized pustular psoriasis in Germany: Analyzing factors influencing prevalence estimates health insurance data. [PDF]

open access: yesJ Dtsch Dermatol Ges
Summary Background and Objectives: Generalized pustular psoriasis (GPP) is a rare, chronic, potentially life‐threatening skin disease. We aimed to establish criteria to accurately approximate GPP prevalence in Germany. Methods: A retrospective analysis of the WIG2 health claims database (1/1/2016–31/12/2020) was conducted.
Schultze M   +4 more
europepmc   +2 more sources

Palmoplantar pustulosis and acrodermatitis continua of Hallopeau: demographic and clinical comparative study in a large multicentre cohort. [PDF]

open access: yesJ Eur Acad Dermatol Venereol, 2022
BACKGROUND: Acral pustular disease within the pustular psoriasis/psoriasis‐like spectrum mainly includes palmoplantar pustulosis (PPP) and acrodermatitis continua of Hallopeau (ACH).
Assan F   +15 more
europepmc   +2 more sources

Challenges of the differential diagnosis between the subtypes of the junctional epidermolysis bullosa: presentation of two clinical cases

open access: yesAlʹmanah Kliničeskoj Mediciny, 2019
Background: Epidermolysis bullosa (EB) is a rare hereditary skin disease. It is subdivided into EB simplex (EBS), junctional EB (JEB), dystrophic EB (DEB) and Kindler syndrome. JEB is diagnosed in 2 per 1,000,000 of the population.
Yu. Yu. Kotalevskaya, N. M. Marycheva
doaj   +1 more source

Chronic Paronychia and Onychomadesis in Pemphigus Vegetans: An Unusual Presentation in a Rare Autoimmune Disease

open access: yesCase Reports in Medicine, 2018
Pemphigus vegetans is a rare variant of deep acantholytic pemphigus which usually presents with vesiculobullous rash and vegetative plaques on the folds. We report a case of pemphigus vegetans patient who presented with rashes on tips of fingers and toes
Thanisorn Sukakul, Supenya Varothai
doaj   +1 more source

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