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A Case of Wegener's Granulomatosis with Delayed Diagnosis due to Clinical Features of Henoch-Schonlein Purpura / 결핵및호흡기질환
Article in Ko | WPRIM | ID: wpr-134814
Responsible library: 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.
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Full text: 1 Index: WPRIM Main subject: Arteries / Arterioles / IgA Vasculitis / Respiratory System / Vasculitis / Venules / Biopsy / Granulomatosis with Polyangiitis / Diagnosis / Systemic Vasculitis Type of study: Diagnostic_studies Language: Ko Journal: Tuberculosis and Respiratory Diseases Year: 2007 Type: Article
Full text: 1 Index: WPRIM Main subject: Arteries / Arterioles / IgA Vasculitis / Respiratory System / Vasculitis / Venules / Biopsy / Granulomatosis with Polyangiitis / Diagnosis / Systemic Vasculitis Type of study: Diagnostic_studies Language: Ko Journal: Tuberculosis and Respiratory Diseases Year: 2007 Type: Article