Systemic Amyloidosis in a Patient with Adult Onset Stills Disease
スポンサーリンク
概要
- 論文の詳細を見る
A 39-year-old woman presented clinical features of adult onset Stills disease. Seven years after the onset, she developed renal insufficiency and biopsy studies revealed amyloid deposits involving amyloid A protein, P component, λ chain and κ chain in the kidney and rectum. She died in 1992, primarily due to cardiac failure associated with amyloidosis, indicating that amyloidosis should be considered one of the fatal complications in adult onset Stills disease with a long history.(Internal Medicine 32: 50-52, 1993)
著者
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Yoshinaga Kaoru
The Second Department Of Internal Medicine Tohoku University School Of Medicine
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KAWANAMI Toru
The Third Department of Internal Medicine, Yamagata University School of Medicine
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Yoshinaga Kaoru
The Second Department of Internal Medicine, Tohoku University School of Medicine
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ISHII Tomonori
the Second Department of Internal Medicine, Tohoku University School of Medicine
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SASAKI Takeshi
the Second Department of Internal Medicine, Tohoku University School of Medicine
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MURYOI Tai
the Second Department of Internal Medicine, Tohoku University School of Medicine
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MURAI Chihiro
the Second Department of Internal Medicine, Tohoku University School of Medicine
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HATAKEYAMA Akira
the Second Department of Internal Medicine, Tohoku University School of Medicine
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OOSAKI Hirofumi
the Second Department of Internal Medicine, Tohoku University School of Medicine
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YUSA Akira
the Second Department of Internal Medicine, Tohoku University School of Medicine
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