A Case of Wells' Syndrome Treated with Systemic PUVA / 대한피부과학회지
Korean Journal of Dermatology
;
: 949-954, 2000.
Artículo
en Coreano
| WPRIM
| ID: wpr-131960
ABSTRACT
Wells' syndrome, or eosinophilic cellulitis, is characterized by recurrent cutaneous swellings which resemble acute bacterial cellulitis, and by distinctive histopathological changes. Skin lesions show dermal eosinophilic infiltration and the characteristic 'flame figures', but not pathognomonic, which are composed of eosinophil major protein deposited on collagen bundles. A 51-year-old woman developed a chronic, pruritic, erythematous to dark-brown colored, annular, infiltrated plaques with papules, vesicles and some crusts on the chest, abdomen, back and both forearms with the clinical and histological features of Wells' syndrome. Skin lesions had recurred frequently with systemic corticosteroids therapy, so we tried systemic PUVA and treated her successfully without recurrence until now.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Recurrencia
/
Piel
/
Tórax
/
Celulitis (Flemón)
/
Colágeno
/
Corticoesteroides
/
Eosinófilos
/
Abdomen
/
Antebrazo
Límite:
Femenino
/
Humanos
Idioma:
Coreano
Revista:
Korean Journal of Dermatology
Año:
2000
Tipo del documento:
Artículo
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