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IgG4-related tubulointerstitial nephritis and hepatic inflammatory pseudotumor without hypocomplementemia
http://hdl.handle.net/2297/28339
http://hdl.handle.net/2297/28339069021a3-3bb3-4c69-92a4-c635613e7d43
名前 / ファイル | ライセンス | アクション |
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HO-PR-KAWANO-M-1239.pdf (1.6 MB)
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Item type | 学術雑誌論文 / Journal Article(1) | |||||
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公開日 | 2017-10-05 | |||||
タイトル | ||||||
タイトル | IgG4-related tubulointerstitial nephritis and hepatic inflammatory pseudotumor without hypocomplementemia | |||||
言語 | ||||||
言語 | eng | |||||
資源タイプ | ||||||
資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||
資源タイプ | journal article | |||||
著者 |
Kim, Fae
× Kim, Fae× Yamada, Kazunori× Inoue, Dai× Nakajima, Kenichi× Mizushima, Ichiro× Kakuchi, Yasushi× Fujii, Hiroshi× Narumi, Kenta× Matsumura, Masami× Umehara, Hisanori× Yamagishi, Masakazu× Kawano, Mitsuhiro |
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提供者所属 | ||||||
内容記述タイプ | Other | |||||
内容記述 | 金沢大学附属病院リウマチ・膠原病内科 | |||||
書誌情報 |
Internal Medicine 巻 50, 号 11, p. 1239-1244, 発行日 2011-01-01 |
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ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 0918-2918 | |||||
NCID | ||||||
収録物識別子タイプ | NCID | |||||
収録物識別子 | AA10827774 | |||||
DOI | ||||||
関連タイプ | isIdenticalTo | |||||
識別子タイプ | DOI | |||||
関連識別子 | 10.2169/internalmedicine.50.5102 | |||||
出版者 | ||||||
出版者 | The Japanese Society of Internal Medicine = 日本内科学会 | |||||
抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | Immunoglobulin G4 (IgG4)-related tubulointerstitial nephritis (TIN) is often accompanied by autoimmune pancreatitis (AIP) or chronic sclerosing dacryoadenitis and sialoadenitis. However, IgG4-related TIN without AIP or lacrimal and/or salivary gland lesions has not been well recognized. Here, we report a case of IgG4-related TIN associated with hepatic inflammatory pseudotumor without AIP or lacrimal and/or salivary gland lesions. A 58-year-old Japanese man with epigastralgia underwent contrast-enhanced computed tomography (CT), which revealed multiple low-density lesions in both kidneys and a low density hepatic mass. Laboratory tests showed an extremely high level of serum IgG4. Percutaneous renal and hepatic biopsies showed diffuse infiltration of lymphocytes and IgG4-positive plasma cells with fibrosis in both tissues. Two months after administration of oral prednisolone, both lesions decreased in size on follow-up CT, and the serum cre-atinine level also improved. No recurrence has been detected for two years with a maintenance dose of pred-nisolone. © 2011 The Japanese Society of Internal Medicine. | |||||
権利 | ||||||
権利情報 | Copyright (c) 2011 by The Japanese Society of Internal Medicine | |||||
著者版フラグ | ||||||
出版タイプ | VoR | |||||
出版タイプResource | http://purl.org/coar/version/c_970fb48d4fbd8a85 | |||||
関連URI | ||||||
識別子タイプ | URI | |||||
関連識別子 | https://japanlinkcenter.org/JST.JSTAGE/internalmedicine/50.5102 | |||||
関連URI | ||||||
識別子タイプ | URI | |||||
関連識別子 | http://www.naika.or.jp/ |