The Efficacy of Interferon-alpha in a Patient with Resistant Familial Mediterranean Fever Complicated by Polyarteritis Nodosa
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概要
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Familial Mediterranean fever (FMF) is a recurrent self-limiting polyserositis. Polyarteritis nodosa (PAN) complicating FMF is very rare. Here, we present a 17-year-old male patient with FMF who subsequently developed PAN 2 weeks after hepatitis A infection. This case was also complicated with perirenal haematoma, and right nephrectomy was performed. The clinical condition of the patient was improved after therapy with intravenous and oral corticosteroid and intravenous cyclophosphamide. However, the FMF attacks and vasculitic skin lesions again occurred while he was using colchicine plus immunosuppressive agents a few months later. Interferon-alpha therapy was administered and the attacks were resolved within 3 months. He has not experienced any other symptom during the follow-up period of 28 months.
- 社団法人 日本内科学会の論文
- 2004-07-01
著者
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Ozturk M.
Gazi University Faculty Of Medicine Internal Medicine Department Section Of Rheumatology
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Apras Sule
Hacettepe University Faculty Of Medicine Internal Medicine Department Section Of Rheumatology
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Calguneri Meral
Hacettepe University Faculty Of Medicine Internal Medicine Department Section Of Rheumatology
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OZBALKAN Zeynep
Hacettepe University Faculty of Medicine, Internal Medicine Department, Section of Rheumatology
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OZBALKAN Zeynep
Ankara Numune Training and Research Hospital, Internal Medicine Department, Section of Rheumatology
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Ozbalkan Zeynep
Ankara Numune Training And Research Hospital Internal Medicine Department Section Of Rheumatology
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