We report a case of an inflammatory variant of epidermolysis bullosa acquisita in a 53-year-old male, with itching blistering eruption on the trunk, armpits and limbs for six months. The skin biopsy specimen showed subepidermal blister with neutrophils. Direct immunofluorescence revealed linear depositions of IgG, IgA, IgM and C3 at the basement membrane; indirect immunofluorescence and salt split skin were negative. Antinuclear antibodies were also negative. Improvement of the blisters followed treatment with systemic corticotherapy and some lesions healed with milia. This is a rare presentation of epidermolysis bullosa acquisita, with inflammatory lesions at first
Epidermolysis bullosa pruriginosa, a genetic mechanobullous disease, is characterized by pruritus, ...
Background The inflammatory variant of epidermolysis bullosa may mimic a form of pemphigoid.Objectiv...
Epidermolysis bullosa acquisita (EBA) is a rare, immunobullous disease, characterized by circulating...
We report a case of an inflammatory variant of epidermolysis bullosa acquisita in a 53-year-old male...
Apresenta-se caso de epidermólise bolhosa adquirida inflamatória. Paciente do sexo masculino, 53 ano...
A 39-year-old woman had a three-year history of recurrent bullous eruption localized to her left che...
The article describes present-day information on the pathogenesis, clinical picture, treatment and d...
A 35 years old man presented with features of epidermolysis bullosa acquisita. Here is the case repo...
Background: The inflammatory variant of epidermolysis bullosa acquisita (EBA) may clinically closely...
Epidermolysis bullosa acquisita (EBA) is an acquired, autoimmune subepidermal blistering disease wit...
Observations: Epidermolysis bullosa is a group of rare disorders which have in common the forma-tion...
A 64-year-old man presented with a bullous eruption which clinically and histopathologically resembl...
We describe 2 adult patients with a subepidermal bullous dermatosis with exclusively linear IgA depo...
P>Background. Epidermolysis bullosa acquisita (EBA) is a subepidermal blistering disease with IgG an...
Epidermolysis bullosa pruriginosa, a genetic mechanobullous disease, is characterized by pruritus, ...
Background The inflammatory variant of epidermolysis bullosa may mimic a form of pemphigoid.Objectiv...
Epidermolysis bullosa acquisita (EBA) is a rare, immunobullous disease, characterized by circulating...
We report a case of an inflammatory variant of epidermolysis bullosa acquisita in a 53-year-old male...
Apresenta-se caso de epidermólise bolhosa adquirida inflamatória. Paciente do sexo masculino, 53 ano...
A 39-year-old woman had a three-year history of recurrent bullous eruption localized to her left che...
The article describes present-day information on the pathogenesis, clinical picture, treatment and d...
A 35 years old man presented with features of epidermolysis bullosa acquisita. Here is the case repo...
Background: The inflammatory variant of epidermolysis bullosa acquisita (EBA) may clinically closely...
Epidermolysis bullosa acquisita (EBA) is an acquired, autoimmune subepidermal blistering disease wit...
Observations: Epidermolysis bullosa is a group of rare disorders which have in common the forma-tion...
A 64-year-old man presented with a bullous eruption which clinically and histopathologically resembl...
We describe 2 adult patients with a subepidermal bullous dermatosis with exclusively linear IgA depo...
P>Background. Epidermolysis bullosa acquisita (EBA) is a subepidermal blistering disease with IgG an...
Epidermolysis bullosa pruriginosa, a genetic mechanobullous disease, is characterized by pruritus, ...
Background The inflammatory variant of epidermolysis bullosa may mimic a form of pemphigoid.Objectiv...
Epidermolysis bullosa acquisita (EBA) is a rare, immunobullous disease, characterized by circulating...