Bullous Congenital Ichthyosiform Erythroderma: Report of a Case / 대한피부과학회지
Korean Journal of Dermatology
;
: 445-501, 1981.
Article
in Korean
| WPRIM
| ID: wpr-104852
ABSTRACT
We present a case of bullous congenital ichthyosiform erythroderma in a two year old female, in whom no hereditary background was found. The skin lesion was characterized clinically by blister formation with generalized erythematous hyperkeratosis which was especially prominent on the flexural surfaces of extremities and intertriginous areas. The histopathologic examination revealed marked hyperkeratosis, cavity changes of the malpighian cells with perinuclear vacuoles and markedly thickened granular layer containing many keratohyaline granules.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Skin
/
Vacuoles
/
Blister
/
Hyperkeratosis, Epidermolytic
/
Extremities
Limits:
Female
/
Humans
Language:
Korean
Journal:
Korean Journal of Dermatology
Year:
1981
Type:
Article
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