A Case of Wells' Syndrome Treated with Systemic PUVA / 대한피부과학회지
Korean Journal of Dermatology
;
: 949-954, 2000.
Article
Dans Coréen
| 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.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Récidive
/
Peau
/
Thorax
/
Cellulite sous-cutanée
/
Collagène
/
Hormones corticosurrénaliennes
/
Granulocytes éosinophiles
/
Abdomen
/
Avant-bras
Limites du sujet:
Femelle
/
Humains
langue:
Coréen
Texte intégral:
Korean Journal of Dermatology
Année:
2000
Type:
Article
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