Epidermolysis bullosa pruriginosa: a rare autosomal dominant variant.
J Indian Med Assoc
;
2007 Jul; 105(7): 388, 390
Artigo
em Inglês
| IMSEAR
| ID: sea-97572
ABSTRACT
A 35 years female presented with extremely pruritic, violaceous, small vesiculopapular lesions over both shins since 11/12 years of age. The intensity of pruritus slightly descreased following oozing of fluid. History of similar incidence in her mother and maternal grandfather was present. There was no toe-nail dystrophy. Histopathology report showed the lesions had hyperkeratotic, mild acanthosis, dermal lymphohistiocytic infiltrate and subepidermal cleft. The case was diagnosed to be a case of epidermolysis bullosa pruriginosa.
Texto completo:
DisponíveL
Índice:
IMSEAR (Sudeste Asiático)
Assunto principal:
Feminino
/
Humanos
/
Epidermólise Bolhosa Distrófica
/
Progressão da Doença
/
Adulto
/
Colágeno Tipo VII
/
Mutação
Idioma:
Inglês
Revista:
J Indian Med Assoc
Ano de publicação:
2007
Tipo de documento:
Artigo
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