Results 11 to 20 of about 5,993 (141)

A Study of Vesiculobullous Lesions of Skin [PDF]

open access: yesNational Journal of Laboratory Medicine, 2018
Introduction: Bullous dermatoses are a wide variety of blistering diseases some of which can be extremely debilitating and even fatal. This study shows the importance of histopathology over immunofluorescence studies in the diagnosis of the same.
Anupama Raj Karattuthazhathu   +2 more
doaj   +1 more source

Pemphigus vulgaris [PDF]

open access: yesAnais Brasileiros de Dermatologia, 2019
: Pemphigus vulgaris is a chronic autoimmune bullous dermatosis that results from the production of autoantibodies against desmogleins 1 and 3. It is the most frequent and most severe form of pemphigus, occurring universally, usually between 40 and 60 ...
Adriana Maria Porro   +3 more
doaj   +1 more source

Oral Mucous Membrane Pemphigoid With Positive Nikolsky’s Sign: A Case Report

open access: yesActa Medica Iranica, 2021
Mucous membrane pemphigoid (MMP) is a rare inflammatory, autoimmune, and subepithelial vesiculobullous disease in which tissue-bound autoantibodies are produced against one or more components of the basement membrane. Oral lesions of the pemphigoid begin
Narjes Akbari   +2 more
doaj   +1 more source

Comorbidities in Patients with Autoimmune Bullous Disorders: Hospital-Based Registry Study

open access: yesLife, 2022
The incidence of autoimmune bullous disorders has increased over the years, especially in elderly patients with multiple comorbidities, which has stimulated research into their association with other diseases.
Verónica Sánchez-García   +3 more
doaj   +1 more source

Comparative scanning electron microscopy of bullous diseases [PDF]

open access: yesAnais Brasileiros de Dermatologia, 2014
The purpose of this study is to compare scanning electron microscopy findings of the blister roof in three distinct bullous diseases: one intraepidermal acantholytic (pemphigus foliaceus); one due to hemidesmosomal dysfunction (bullous pemphigoid); and ...
Hiram Larangeira de Almeida Jr   +4 more
doaj   +2 more sources

Bullous systemic lupus erythematosus in a 10-year-old child [PDF]

open access: yesAnais Brasileiros de Dermatologia, 2017
: Bullous systemic lupus erythematosus (BSLE) is a rare autoimmune subepidermal blistering disease, with few cases described in childhood. It has different clinical-pathological features.
Nelise Ritter Hans-Bittner   +3 more
doaj   +1 more source

Review: dermatitis herpetiformis [PDF]

open access: yesAnais Brasileiros de Dermatologia, 2013
Dermatitis herpetiformis (DH) or Duhring-Brocq disease is a chronic bullous disease characterized by intense itching and burning sensation in the erythematous papules and urticarial plaques, grouped vesicles with centrifuge growth, and tense blisters ...
Fernanda Berti Rocha Mendes   +3 more
doaj   +1 more source

Linear IgA bullous dermatosis: report of an exuberant case [PDF]

open access: yesAnais Brasileiros de Dermatologia, 2013
Linear immunoglobulin A dermatosis is a rare autoimmune bullous disease, but the most common autoimmune bullous dermatosis in children. We report a typical exuberant case of linear IgA dermatosis in a ten-month old child, who showed good response to ...
Beatriz Cavalcanti de Souza   +5 more
doaj   +1 more source

A comparative study of expression of Fc receptors in relation to the autoantibody-mediated immune response and neutrophil elastase expression in autoimmune blistering dermatoses

open access: yesPolish Journal of Pathology, 2017
Here we investigated the cutaneous CD32A and CD89 expression in relation to the neutrophil elastase (NE) expression and serum level of anti-desmoglein 1 and 3 (DSG1/DSG3) IgG in pemphigus, anti-BP180/BP230 IgG in bullous pemphigoid (BP), anti-gliadin ...
Justyna Gornowicz-Porowska   +6 more
doaj   +1 more source

Subcorneal pustular dermatosis: Eleven years of experience in a national reference center. Report of cases

open access: yesIatreia, 2023
Subcorneal pustular dermatosis is a rare and little known dermatosis. The objective of this paper is to describe the experience of the authors in the diagnosis and treatment of a group of Colombian patients with this disea-se.
Verónica Sánchez-González   +2 more
doaj   +1 more source

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