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Desmosomal-Type Acantholysis—A New Histologic Pattern Related to Mutations of Genes for Desmosomal Proteins [PDF]

open access: yesDermatopathology
Desmosomes are specialized cell–cell junctions that play a crucial role in maintaining the structural integrity of both cornifying and non-cornifying epithelium. Disruption of desmosomal cohesion in autoimmune, infectious, and other diseases is typically
Dieter Metze   +4 more
doaj   +2 more sources

Caspase-activation powers anti-Desmoglein 3-induced acantholysis in human epidermis [PDF]

open access: yesCell Death Discovery
Pemphigus vulgaris (PV) is a life-threatening autoimmune blistering disease caused by circulating autoantibodies against desmoglein (Dsg) 1 and Dsg 3.
Morna F. Schmidt   +10 more
doaj   +3 more sources

Evaluation of the possible association between acantholysis and anti‐desmogleins 1 and 3 values in pemphigus vulgaris and pemphigus foliaceus

open access: yesJournal of Cutaneous Immunology and Allergy, 2019
Objectives Acantholysis is the main pathologic finding in pemphigus, and its location has been historically used to distinguish the major subtypes of pemphigus vulgaris (PV) and pemphigus foliaceus (PF).
Nazanin Rajai, Azita Nikoo, Ali Nili
exaly   +2 more sources

Mechanisms of Acantholysis in Pemphigus: Mechanical or Inflammatory?

open access: yesEuropean Journal of Inflammation, 2006
Pemphigus is a rare autoimmune disease, involving the skin and mucous epithelia, characterized by flaccid blisters and erosions. Histologically, the basic abnormality in all forms of pemphigus is the separation of keratinocytes from one another, a ...
Giacomo Caldarola, Claudio Feliciani
exaly   +2 more sources

Caspase Inhibition as a Possible Therapeutic Strategy for Pemphigus Vulgaris: A Systematic Review of Current Evidence

open access: yesBiology, 2022
Background: Pemphigus vulgaris (PV) is an IgG-mediated autoimmune disease characterised by epithelial cell–cell detachment (acantholysis) resulting in mucocutaneous blistering.
Sanna Huda   +5 more
doaj   +1 more source

Post-Pemphigus Acanthomata Presenting as an Isolated, Hyperkeratotic Plaque

open access: yesDermatopathology, 2023
Post-pemphigus acanthomas have been rarely discussed in the literature. A prior case series identified 47 cases of pemphigus vulgaris and 5 cases of pemphigus foliaceus, out of which 13 developed acanthomata as a part of the healing process. Additionally,
Rachita Pandya   +4 more
doaj   +1 more source

Spongiotic Pattern in Pemphigus: A Retrospective Observational Single-Center Study

open access: yesDermatopathology, 2022
Pemphigus is a chronic blistering disorder caused by autoantibodies that target desmosomal proteins in the epidermis. Acantholysis may be absent, and pemphigus may present only with spongiosis and vesiculation, thereby leading to a misdiagnosis of eczema.
Ivan Arni C. Preclaro, Yu-Hung Wu
doaj   +1 more source

Innate immune activation as cofactor in pemphigus disease manifestation

open access: yesFrontiers in Immunology, 2022
Molecular mechanisms underlying auto-antibody-induced acantholysis in pemphigus vulgaris are subject of current research to date. To decipher the discrepancy between ubiquitous antibody binding to the epidermal desmosomes, but discontinuous disease ...
Ramona A. Eichkorn   +7 more
doaj   +1 more source

Pemphigus vulgaris: A rare case of gingival involvement

open access: yesContemporary Clinical Dentistry, 2020
Pemphigus vulgaris (PV) is an autoimmune mucocutaneous disease characterized by epithelial blistering affecting the mucosal/cutaneous surfaces. This case report demonstrates the oral manifestations of PV in the uncommon locations such as the attached ...
Nisha Thakur   +3 more
doaj   +1 more source

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