Dominant Dystrophic Epidermolysis Bullosa / 대한피부과학회지
Korean Journal of Dermatology
;
: 889-892, 2010.
Artigo
em Coreano
| WPRIM
| ID: wpr-182728
ABSTRACT
Dystrophic epidermolysis bullosa is a rare, chronic non-inflammatory bullous disease with a hereditary pattern of occurrence, and this disease easily produces bullae that heal with scarring and milium formation. A 13-month-old female baby was brought to the department of dermatology with multiple variable sized bullae and erythematous to dark brownish patches and crusts on both her feet. The histopathologic findings showed subepidermal non-inflammatory blisters and the electron microscopic findings showed vacuolization of the sublamina densa and broken anchoring fibrils. On the basis of the clinical and microscopic findings, she was diagnosed as having dominant dystrophic epidermolysis bullosa. We report here on a case of dominant dystrophic epidermolysis bullosa with the clinical, histological and electron microscopic findings, as well as the family history of the patient.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Epidermólise Bolhosa Distrófica
/
Epidermólise Bolhosa Simples
/
Vesícula
/
Cicatriz
/
Dermatologia
/
Elétrons
/
Pé
Limite:
Feminino
/
Humanos
/
Lactente
Idioma:
Coreano
Revista:
Korean Journal of Dermatology
Ano de publicação:
2010
Tipo de documento:
Artigo
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