Ticlopidine Treatment in Idiopathic Plasmacytic Lymphadenopathy with Polyclonal Hyperimmunoglobulinemia Accompanied by Nephrotic Syndrome.
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- KATO Yoshiro
- the Second Department of Internal Medicine, Aichi Medical College
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- KOBAYASHI Hideo
- the Second Department of Internal Medicine, Aichi Medical College
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- MIHARA Hidetsugu
- the Second Department of Internal Medicine, Aichi Medical College
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- MIZUTANI Yasuko
- the Second Department of Internal Medicine, Aichi Medical College
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- KAMIJIMA Shinsuke
- the Second Department of Internal Medicine, Aichi Medical College
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- TANAKA Akihiko
- the Second Department of Internal Medicine, Aichi Medical College
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- TAKEDA Hiroyuki
- the Second Department of Internal Medicine, Aichi Medical College
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- KATO Ryoichi
- the Second Department of Internal Medicine, Aichi Medical College
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- OGURI Takashi
- the Second Department of Internal Medicine, Aichi Medical College
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A 36-year-old woman was admitted for idiopathic plasmacytic lymphadenopathy with polyclonal hyperimmunoglobulinemia (IPL) associated with nephrotic syndrome. She was expected to lapse into renal failure because renal biopsy showed focal glomerulosclerosis. VEMP chemotherapy and bolus methyl prednisolone were not effective against excessive urine protein of over 10g/day. We thus began administration of ticlopidine (6mg/kg/day), prednisolone (0.4mg/kg/day) and cyclophosphamide (1mg/kg/day). After 3 months of this regimen, the urine protein level decreased to less than 0.5g/day, and renal function was maintained for more than 3 years. It is suggested that ticlopidine is effective for nephropathy complications associated with IPL.<br>(Internal Medicine 31 : 504-507, 1992)
収録刊行物
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- Internal Medicine
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Internal Medicine 31 (4), 504-507, 1992
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
- 1390282679843763968
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- NII論文ID
- 130000770033
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- NII書誌ID
- AA10827774
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- COI
- 1:STN:280:By2A3sfkslw%3D
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- ISSN
- 13497235
- 09182918
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- PubMed
- 1633358
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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
- Crossref
- PubMed
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可