Epidermolysis bullosa pruriginosa: a rare autosomal dominant variant.
J Indian Med Assoc
;
2007 Jul; 105(7): 388, 390
Artículo
en Inglés
| 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:
Disponible
Índice:
IMSEAR (Asia Sudoriental)
Asunto principal:
Femenino
/
Humanos
/
Epidermólisis Ampollosa Distrófica
/
Progresión de la Enfermedad
/
Adulto
/
Colágeno Tipo VII
/
Mutación
Idioma:
Inglés
Revista:
J Indian Med Assoc
Año:
2007
Tipo del documento:
Artículo
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