A Case of Wegener's Granulomatosis with Delayed Diagnosis due to Clinical Features of Henoch-Schonlein Purpura / 결핵및호흡기질환
Tuberculosis and Respiratory Diseases
; : 531-536, 2007.
Artigo
em Coreano
| WPRIM (Pacífico Ocidental)
| ID: wpr-134814
Biblioteca responsável:
WPRO
ABSTRACT
Wegener's granulomatosis is a systemic vasculitis of the medium and small arteries, as well as of the venules, arterioles, and occasionally large arteries, and primarily involves the upper and lower respiratory tracts and the kidneys. Renal symptoms of Wegener's granulomatosis are indistinguishable from those of vasculitis such as Henoch-Schonlein purpura and microscopic polyangiitis. This case, though initially diagnosed as Henoch-Schonlein purpura, was confirmed as Wegener's granulomatosis from a lung biopsy fifteen years after the initial diagnosis. We report this case with a review of the literature.
Texto completo:
Disponível
Base de dados:
WPRIM (Pacífico Ocidental)
Assunto principal:
Artérias
/
Arteríolas
/
Vasculite por IgA
/
Sistema Respiratório
/
Vasculite
/
Vênulas
/
Biópsia
/
Granulomatose com Poliangiite
/
Diagnóstico
/
Vasculite Sistêmica
Tipo de estudo:
Estudo diagnóstico
Idioma:
Coreano
Revista:
Tuberculosis and Respiratory Diseases
Ano de publicação:
2007
Tipo de documento:
Artigo