A Case of Epidermolysis Bullosa Acquisita with Pseudomembranous Esophageal Involvement / 대한피부과학회지
Korean Journal of Dermatology
;
: 1289-1292, 2002.
Artigo
em Coreano
| WPRIM
| ID: wpr-126838
ABSTRACT
Epidermolysis bullosa acquisita (EBA) is an acquired subepidermal blistering disorder characterized by autoantibodies to anchoring fibril (type VII) collagen. EBA is known to have a wide clinical spectrum that includes a non-inflammatory mechanobullous presentation, an inflammatory vesiculobullous eruption akin to bullous pemphigoid, and a mucosal centered disease with scarring that is reminiscent of cicatrical pemphigoid. Patients with EBA often have lesions on the oral mucosa, but esophageal involvement has not been well documented. We report a case of EBA in a 63-year-old woman who had a pseudomembranous esophageal lumen. To our knowledge, this is the first report of EBA with pseudomembranous esophageal involvement.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Autoanticorpos
/
Epidermólise Bolhosa Adquirida
/
Vesícula
/
Colágeno
/
Epidermólise Bolhosa
/
Cicatriz
/
Penfigoide Bolhoso
/
Esôfago
/
Mucosa Bucal
Limite:
Feminino
/
Humanos
Idioma:
Coreano
Revista:
Korean Journal of Dermatology
Ano de publicação:
2002
Tipo de documento:
Artigo
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