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A Case of Polyarteritis Nodosa Mimicking Systemic Lupus Erythematosus / 대한류마티스학회지
The Journal of the Korean Rheumatism Association ; : 427-430, 2007.
Article in Korean | WPRIM | ID: wpr-227627
ABSTRACT
Polyarteritis nodosa (PAN) is a rare systemic necrotizing vasculitis involving multiple organ system. Systemic lupus erythematousus (SLE) also presented as a vasculitic symptoms. So, systemic vasculitis and SLE share some clinical features. We report a case of polyarteritis nodosa mimicking SLE. A 45-year-old woman was admitted due to oliguria. She diagnosed SLE because of pericardial effusion, hemolytic anemia, proteinuria, hematuria, and positivity of anti-dsDNA antibody. But she re-diagnosed as PAN through renal angiography and renal biopsy afterwards. She was treated with high dose steroid, cyclophosphamide, and anti-TNF-alpha antibody, but didn't respond those therapies.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Oliguria / Polyarteritis Nodosa / Pericardial Effusion / Proteinuria / Vasculitis / Biopsy / Angiography / Cyclophosphamide / Systemic Vasculitis / Hematuria Limits: Female / Humans Language: Korean Journal: The Journal of the Korean Rheumatism Association Year: 2007 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Oliguria / Polyarteritis Nodosa / Pericardial Effusion / Proteinuria / Vasculitis / Biopsy / Angiography / Cyclophosphamide / Systemic Vasculitis / Hematuria Limits: Female / Humans Language: Korean Journal: The Journal of the Korean Rheumatism Association Year: 2007 Type: Article