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.
Artículo
en Coreano
| WPRIM
| ID: wpr-134815
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:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Arterias
/
Arteriolas
/
Vasculitis por IgA
/
Sistema Respiratorio
/
Vasculitis
/
Vénulas
/
Biopsia
/
Granulomatosis con Poliangitis
/
Diagnóstico
/
Vasculitis Sistémica
Tipo de estudio:
Estudio diagnóstico
Idioma:
Coreano
Revista:
Tuberculosis and Respiratory Diseases
Año:
2007
Tipo del documento:
Artículo
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