A Case of Epidermolysis Bullosa Dystrophica / 대한피부과학회지
Korean Journal of Dermatology
;
: 387-391, 1985.
Artigo
em Coreano
| WPRIM
| ID: wpr-106116
ABSTRACT
Epidermolysis bullosa dystrophica(EBD) is a rare, hereditary and chronic mechanobullous disease characterized by blistering and erosions of the skin in response to even minor trauma. A 5-year old girl visited with a complaint of continuous vesicobullous skin eruptions since birth. On examination, bullae, vesicles, atrophic scars, crusts and eroions were scattered on whole body. Loss of finger and toe nails, partial syndactyly of all toe webs and milia on dorsa of feet were noticed. We present a case of EBD that seems to be a recessive type considering the absence of family history with histopathologic and electron microscopic findings.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Pele
/
Dedos do Pé
/
Epidermólise Bolhosa Distrófica
/
Vesícula
/
Epidermólise Bolhosa
/
Cicatriz
/
Sindactilia
/
Parto
/
Dedos
/
Pé
Limite:
Criança, pré-escolar
/
Feminino
/
Humanos
Idioma:
Coreano
Revista:
Korean Journal of Dermatology
Ano de publicação:
1985
Tipo de documento:
Artigo
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