A Case of Churg-Strauss Syndrome With Acute Glomerulonephritis / 대한피부과학회지
Korean Journal of Dermatology
;
: 995-999, 2001.
Artigo
em Coreano
| WPRIM
| ID: wpr-160304
ABSTRACT
Churg-Strauss syndrome is a rare systemic vasculitis diagnosed by the presence of any four or more of six criteria which include asthma, eosinophilia>10%, mono- or poly-neuropathy, nonfixed pulmonary infiltrate, paranasal sinus abnormality, extravascular eosinophils. In a 65 year-old-woman, multiple purpura and crusted ulcer with central necrosis were developed on the both extremities and buttocks 1 month ago. She has been suffered from asthma, sinusitis and recurrent pneumonia since ten years ago Laboratory findings showed hematuria, hypereosinophilia and hyperIgE. On the histological examination of ulcerative nodule on the right leg, leukocytoclastic vasculitis and many neutrophils and eosinophils around the cutaneous vessels were seen and the other findings were fibrinoid necrosis and thickening of vessels wall without eosinophilic granulomatous changes. Renal biopsy showed focal segmental glomerulonephritis and sclerosing nephritis. We report a rare case of Churg-Strauss syndrome with acute glomerulonephritis.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Pneumonia
/
Púrpura
/
Asma
/
Sinusite
/
Úlcera
/
Vasculite
/
Biópsia
/
Nádegas
/
Síndrome de Churg-Strauss
/
Eosinófilos
Idioma:
Coreano
Revista:
Korean Journal of Dermatology
Ano de publicação:
2001
Tipo de documento:
Artigo
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