Worsening Fluid Retention in a Patient with Hereditary Angioedema and End-stage Renal Disease
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- OHSAWA Isao
- Internal Medicine II, Nihon University School of Medicine
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- SATOMURA Atsushi
- Internal Medicine II, Nihon University School of Medicine
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- FUKE Yoshinobu
- Internal Medicine II, Nihon University School of Medicine
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- HIDAKA Mutsuko
- Internal Medicine II, Nihon University School of Medicine
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- ENDO Morito
- Internal Medicine II, Nihon University School of Medicine
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- FUJITA Takayuki
- Internal Medicine II, Nihon University School of Medicine
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- OHI Hiroyuki
- Internal Medicine II, Nihon University School of Medicine
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A 60-year-old woman who was diagnosed with hereditary angioedema (HAE) developed nephrotic syndrome, with end-stage renal disease (ESRD) occurring about 2.5 years later. During her slide toward ESRD, she experienced three severe episodes of angioedema that each resulted in significant fluid retention. Though the therapeutic administration of C1-inhibitor concentrate was effective in controlling her angioedema, seemed ineffective in preventing her from developing ESRD requiring hemodialysis treatment. We theorized that the patient’s low colloid osmolality and glomerular perfusion were important facilitators of her attacks of angioedema.
収録刊行物
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- Internal Medicine
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Internal Medicine 43 (8), 708-712, 2004
一般社団法人 日本内科学会
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詳細情報 詳細情報について
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- CRID
- 1390282679844891520
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- NII論文ID
- 130000084887
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- NII書誌ID
- AA10827774
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- COI
- 1:STN:280:DC%2BD2crgtVGktA%3D%3D
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- ISSN
- 13497235
- 09182918
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- NDL書誌ID
- 7059639
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- PubMed
- 15468971
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- NDL
- Crossref
- PubMed
- CiNii Articles
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- 使用不可