A Case of Churg-Strauss Syndrome Showing Severe Skin Necrosis / 대한피부과학회지
Korean Journal of Dermatology
; : 216-219, 2006.
Article
de Ko
| WPRIM
| ID: wpr-11583
Bibliothèque responsable:
WPRO
ABSTRACT
Churg-Strauss syndrome is a disorder characterized by asthma, fever, systemic vasculitis, extravascular granulomas and hypereosinophilia. A 70-year-old woman with a 2-year history of bronchial asthma was admitted to hospital, due to extensive hemorrhagic bullae embedded in necrotic tissue on both extremities, the buttocks and trunk. The patient showed abnormal laboratory findings including significant peripheral blood eosinophilia and p-ANCA (+), and histopathologically leukocytoclastic vasculitits with marked eosinophlilic infiltration. Based on the clinical course, laboratory data and pathologic findings, the diagnosis of Churg-Strauss syndrome was made. Treatment with oral prednisolone was started, and the clinical findings improved.
Mots clés
Texte intégral:
1
Indice:
WPRIM
Sujet Principal:
Asthme
/
Peau
/
Fesses
/
Prednisolone
/
Syndrome de Churg-Strauss
/
Anticorps anti-cytoplasme des polynucléaires neutrophiles
/
Diagnostic
/
Éosinophilie
/
Membres
/
Vascularite systémique
Type d'étude:
Diagnostic_studies
Limites du sujet:
Aged
/
Female
/
Humans
langue:
Ko
Texte intégral:
Korean Journal of Dermatology
Année:
2006
Type:
Article