書誌事項
- タイトル別名
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- A Case of Bence Jones Protein Kappa Type Myeloma with Adult Fanconi syndrome
- セイヒトガタ Fanconi ショウコウグン オ テイシタ Bence Jon
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Recently we experienced adult Fanconi syndrome seemed as being secondary to Bence Jones protein kappa type myeloma.<br>The patient was a thirty-one year old man who had had glycosuria and proteinuria since about seven years. In the bone marrow were observed myeloma cells containing needle-shaped cytoplasmic inclusion bodies. Bence Jones protein kappa type was detected by urine protein immunoelectrophoresis. Kidney biopsy specimen showed remarkable deposition of protein-like bodies in proximal tubules.<br>In the future, the presence of plasma cell dyscrasia should be taken into consideration in patients with adult Fanconi syndrome.<br>However, monoclonal increase of immunoglobulin is rare in this type of myeloma, therefore, it appears necessary to detect Bence Jones protein thoroughly by such means as urine protein immunoelectrophoresis.
収録刊行物
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- 臨床血液
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臨床血液 19 (3), 234-239, 1978
一般社団法人 日本血液学会
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詳細情報 詳細情報について
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- CRID
- 1390282680012265728
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- NII論文ID
- 130004497931
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- NII書誌ID
- AN00252940
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- COI
- 1:STN:280:CSaD3s%2FgvFw%3D
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- ISSN
- 18820824
- 04851439
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- NDL書誌ID
- 1936647
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- PubMed
- 100635
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- 本文言語コード
- ja
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- データソース種別
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- JaLC
- NDL
- PubMed
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可