Results 51 to 60 of about 2,893 (176)

What Matters Most: A Case of Pemphigus Vulgaris in a Nonagenarian Physician

open access: yes
Journal of the American Geriatrics Society, EarlyView.
Svetlana Bagdasarov   +6 more
wiley   +1 more source

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

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   +1 more source

Painful Mucocutaneous Blistering in a Young Male Patient: A Quiz

open access: yesActa Dermato-Venereologica
is missing (Quiz)
Anna-Maria Forster   +2 more
doaj   +1 more source

ECMO Support in Paraneoplastic Pemphigus With Respiratory Failure: A Case Report With Immune Cell Monitoring

open access: yesClinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Paraneoplastic pemphigus (PNP) is a life‐threatening autoimmune blistering disease with a mortality rate of 70%–90%, driven largely by respiratory complications such as bronchiolitis obliterans. Managing respiratory failure in these patients remains exceptionally difficult.
Lu Li   +5 more
wiley   +1 more source

Cutaneous Horn-Like Papule on the Trunk: Warty Dyskeratoma on an Unusual Location

open access: yesپزشکی بالینی ابن سینا, 2016
Introduction: Warty dyskeratoma (WD) is an uncommon and benign skin lesion that presents as a single papule or nodule with a keratin-filled center.
A.A. Rezanezhad   +4 more
doaj  

Darier disease: Histopathology revisited

open access: yesIndian Journal of Pathology and Microbiology
Darier disease (DD) is a rare genodermatosis. Literature on this topic is overwhelmingly dominated by case reports with rare clinical presentations, which have mentioned the histopathologic features briefly.
Archana Manohar   +3 more
doaj   +1 more source

Grover's disease: dermoscopy, reflectance confocal microscopy, and histopathological correlation

open access: yesDermatology Practical & Conceptual, 2017
Grover’s disease is a benign condition of unknown origin characterized clinically by an erythematous papulovesicular eruption and histopathologically by intraepidermal clefting and four different patterns of acantholysis: Darier-like, pemphigus-like ...
Francesco Lacarrubba   +4 more
doaj   +1 more source

Phosphoprotein Synthesis in Epidermis During Acantholysis

open access: yesExperimental Biology and Medicine, 1969
SummaryThe effect of the acantholytic agent, cantharidin, on several biosynthetic systems was examined with epidermal tissue slices. Cantharidin is an effective inhibitor of protein synthesis, it stimulates RNA synthesis, and it leads to extensive phosphorylation of proteins.
R H, Decker, N J, McMahon
openaire   +2 more sources

Therapeutic Options for IgA Pemphigus in Patients Refractory to Dapsone

open access: yesJEADV Clinical Practice, Volume 5, Issue 2, Page 415-424, June 2026.
ABSTRACT 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 significant role of dapsone as the first‐line treatment.
Lorenz Frasheri   +2 more
wiley   +1 more source

Non-Desmoglein Antibodies in Patients With Pemphigus Vulgaris

open access: yesFrontiers in Immunology, 2018
Pemphigus vulgaris (PV) is a potentially life-threatening mucocutaneous autoimmune blistering disease. Patients develop non-healing erosions and blisters due to cell–cell detachment of keratinocytes (acantholysis), with subsequent suprabasal ...
Kyle T. Amber   +4 more
doaj   +1 more source

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