神戸大学附属図書館デジタルアーカイブ
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学内刊行物
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https://hdl.handle.net/20.500.14094/0100491443
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2025-05-24
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0100491443 (fulltext)
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1.81 MB
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メタデータID
0100491443
アクセス権
open access
出版タイプ
Accepted Manuscript
タイトル
IgA nephropathy in a boy with frequently relapsing nephrotic syndrome
著者
Ichikawa, Yuta ; Horinouchi, Tomoko ; Tanaka, Yu ; Ueda, Chika ; Kitakado, Hideaki ; Kondo, Atsushi ; Sakakibara, Nana ; Yoshikawa, Norishige ; Nozu, Kandai
著者名
Ichikawa, Yuta
著者ID
A2532
研究者ID
1000030754593
ORCID
0000-0003-1655-6030
KUID
https://kuid-rm-web.ofc.kobe-u.ac.jp/search/detail.html?systemId=050f3887e6a59356520e17560c007669
著者名
Horinouchi, Tomoko
堀之内, 智子
ホリノウチ, トモコ
所属機関名
医学部附属病院
著者名
Tanaka, Yu
著者ID
A3398
KUID
https://kuid-rm-web.ofc.kobe-u.ac.jp/search/detail.html?systemId=1daabfccb982e297520e17560c007669
著者名
Ueda, Chika
上田, 知佳
ウエダ, チカ
所属機関名
医学部附属病院
著者ID
A3433
KUID
https://kuid-rm-web.ofc.kobe-u.ac.jp/search/detail.html?systemId=aff7d2fcc0ea7e1e520e17560c007669
著者名
Kitakado, Hideaki
北角, 英晶
キタカド, ヒデアキ
所属機関名
医学研究科
著者ID
A3176
研究者ID
1000030936076
KUID
https://kuid-rm-web.ofc.kobe-u.ac.jp/search/detail.html?systemId=f9d169de91b89fa5520e17560c007669
著者名
Kondo, Atsushi
近藤, 淳
コンドウ, アツシ
所属機関名
医学部附属病院
著者ID
A3093
研究者ID
1000090814319
KUID
https://kuid-rm-web.ofc.kobe-u.ac.jp/search/detail.html?systemId=87805f1de4c169a8520e17560c007669
著者名
Sakakibara, Nana
榊原, 菜々
サカキバラ, ナナ
所属機関名
医学研究科
著者名
Yoshikawa, Norishige
著者ID
A1366
研究者ID
1000070362796
KUID
https://kuid-rm-web.ofc.kobe-u.ac.jp/search/detail.html?systemId=cfe7f9e40ab7db60520e17560c007669
著者名
Nozu, Kandai
野津, 寛大
ノヅ, カンダイ
所属機関名
医学研究科
言語
English (英語)
収録物名
CEN Case Reports
巻(号)
13(1)
ページ
14-18
出版者
Springer Nature
刊行日
2024-02
公開日
2024-08-22
注記
Published online: 24 April 2023
抄録
A Japanese boy developed nephrotic syndrome (NS) and had microscopic hematuria at 8 years old. Renal biopsy was performed. Light microscopy study revealed mesangial proliferation and all immunofluorescent stains (including IgA) were negative, so he was diagnosed with non-IgA diffuse mesangial proliferation (DMP). Complete remission was achieved at 13 days after the initiation of oral prednisolone, and hematuria also disappeared 3 days later, but the patient developed frequently relapsing nephrotic syndrome. Cyclosporine A (CyA) was introduced at 10 years old, and there were no relapses between then and when it was discontinued at 12 years old. A second renal biopsy revealed minimal change without CyA nephrotoxicity. However, there was repeated relapse of NS after discontinuation, so CyA was reintroduced 8 months later, and NS remained in remission thereafter. Microscopic hematuria appeared at 13 years old, however, with gross hematuria appearing at the time of infection. A third renal biopsy revealed mesangial proliferation with IgA-dominant deposition, so the patient was diagnosed with IgA nephropathy. Currently (14 years old), CyA treatment has been discontinued and the patient is undergoing lisinopril therapy for IgA nephropathy, but there are still relapses of NS. To the best of our knowledge, there have been no previous reports of a patient with non-IgA DMP at the onset of NS who had later development of IgA nephropathy. The patient showed non-IgA DMP at the onset, suggesting that NS with non-IgA DMP and IgA nephropathy has some common pathophysiology. Treatment for NS, such as PSL and/or CyA treatment, may suppress the clinical manifestation of late IgA nephropathy.
キーワード
Nephrotic syndrome (NS)
Non-IgA diffuse mesangial proliferation (DMP)
Frequently relapsing nephrotic syndrome (FRNS)
Cyclosporine A (CyA)
IgA nephropathy
カテゴリ
医学研究科
医学部附属病院
学術雑誌論文
権利
This version of the article has been accepted for publication, after peer review (when applicable) and is subject to Springer Nature's AM terms of use, but is not the Version of Record and does not reflect post-acceptance improvements, or any corrections. The Version of Record is available online at: https://doi.org/10.1007/s13730-023-00791-w
関連情報
DOI
https://doi.org/10.1007/s13730-023-00791-w
PMID
37088833
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資源タイプ
journal article
eISSN
2192-4449
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