A Case of Acrokeratoelastoidosis / 대한피부과학회지
Korean Journal of Dermatology
; : 1574-1577, 2004.
Article
em Ko
| WPRIM
| ID: wpr-147533
Biblioteca responsável:
WPRO
ABSTRACT
Acrokeratoelastoidosis (AKE) is a rare skin disorder initially described by Costa, which is inherited by autosomal dominant, but also may be sporadic. Clinically, it consists of small, firm papules with occasional keratosis or umbilication, characteristically along the margins of hands and feet. Histopathologically, it shows hyperkeratosis, acanthosis in the epidermis and fragmentation and rarefaction of elastic fibers-elastorrhexis-in the dermis. A 32-year-old man presented with multiple papules along the border of the hands and feet, and from histopathology, AKE was diagnosed. Herein we report a case of acrokeratoelastoidosis and review the clinical and histopathologic features, etiology, differential diagnosis and treatment.
Palavras-chave
Texto completo:
1
Índice:
WPRIM
Assunto principal:
Pele
/
Derme
/
Diagnóstico Diferencial
/
Epiderme
/
Pé
/
Mãos
/
Ceratose
Tipo de estudo:
Diagnostic_studies
Limite:
Adult
/
Humans
Idioma:
Ko
Revista:
Korean Journal of Dermatology
Ano de publicação:
2004
Tipo de documento:
Article