Results 11 to 20 of about 95,258 (181)

Systemic retinoids for treatment of recalcitrant IgA pemphigus [PDF]

open access: yesOrphanet Journal of Rare Diseases, 2018
IgA pemphigus is an exceedingly rare autoimmune blistering disorder, caused by IgA autoantibodies against desmosomal proteins. No treatment option has been found to be universally effective.
Franziska Schauer   +2 more
doaj   +2 more sources

An Updated Review of Pemphigus Diseases

open access: yesMedicina, 2021
Clinicians may encounter a variety of skin conditions that present with vesiculobullous lesions in their everyday practice. Pemphigus vulgaris, pemphigus foliaceus, IgA pemphigus, and paraneoplastic pemphigus represent the spectrum of autoimmune bullous ...
Ali M. Malik   +5 more
doaj   +2 more sources

A case of IgA pemphigus, with a poor response to dapsone, successfully treated with adalimumab [PDF]

open access: yesClinical Case Reports
Key Clinical Message IgA pemphigus is usually treated by Dapsone. Recalcitrant cases may be treated by Colchicine, Sulfapyridine, or Acitretin. Some patients with recurrent severe disease may not respond to the aforementioned medications.
Saman Al‐Zahawi   +2 more
doaj   +2 more sources

IgG/IgA-pemphigus — extremely rare blistering autoimmune diseases [PDF]

open access: yesVestnik Dermatologii i Venerologii, 2020
Purpose. To present a clinical case of IgG/IgA pemphigus in a 32-year-old woman. Material and methods. Clinical and laboratory examinations were performed to diagnose the disease: cytological examination of an impression smear from the bottom of the ...
Arfenya E. Karamova   +4 more
doaj   +5 more sources

The importance of direct immunofluorescence in pemphigus herpetiformis diagnosis [PDF]

open access: yesAnais Brasileiros de Dermatologia, 2017
Pemphigus herpetiformis is an autoimmune bullous disease, that combines clinical features of dermatitis herpetiformis and linear IgA bullous dermatosis and immunological characteristics of pemphigus, which makes this disease peculiar and this diagnosis ...
Paula Carolina Pessanha de Faria   +5 more
doaj   +2 more sources

Therapeutic Options for IgA Pemphigus in Patients Refractory to Dapsone

open access: yesJEADV Clinical Practice
IgA pemphigus is a rare autoimmune blistering disorder with limited therapeutic guidance available due to its rarity and complex presentation. This comprehensive analysis evaluates the therapeutic outcomes of 67 published patients, emphasising the ...
Lorenz Frasheri   +2 more
doaj   +2 more sources

A Unified Concept of Skin Failure: Primary and Secondary Forms [PDF]

open access: yesInt Wound J
International Wound Journal, Volume 23, Issue 10, October 2026.
Anna B. Chapman, Christopher B. Bunker
wiley   +2 more sources

Case Report: A rare co-occurrence of IgA pemphigus and pyoderma gangrenosum associated with IgA-κ type monoclonal gammopathy of undetermined significance: a 19-year diagnostic and therapeutic journey [PDF]

open access: yesFrontiers in Immunology
We report a complex case of neutrophilic dermatosis (ND) in a 61-year-old woman with a 19-year history of recurrent, pruritic, and painful vesiculopustular eruptions.
You Xie   +9 more
doaj   +2 more sources

European S2k guidelines on management of autoimmune blistering diseases in children and adolescents [PDF]

open access: yesJournal of the European Academy of Dermatology and Venereology, Volume 40, Issue 7, Page 1137-1161, July 2026.
Autoimmune blistering disorders (AIBDs) in children are rare, challenging to diagnose and treat and often require immunosuppressants. Until now, no paediatric care guidelines existed. The EADV Task Force for AIBDs has developed the consensus‐based recommendations, enabling physicians to adopt a uniform, tailored treatment strategy to improve outcomes ...
A. Nanda   +31 more
wiley   +2 more sources

Unraveling the autoimmune architecture of pemphigus: from B-cell depletion to network-based immune engineering [PDF]

open access: yesFrontiers in Immunology
Pemphigus encompasses autoimmune blistering diseases driven by autoantibodies to desmosomal proteins. Disruption of keratinocyte adhesion produces acantholysis and epidermal fragility.
Pedram Shafiei-Jahani   +10 more
doaj   +2 more sources

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