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dc.contributor.author高田, 昌幸ja
dc.contributor.author三好, 満ja
dc.contributor.author河野, 眞範ja
dc.contributor.author伊藤, 正典ja
dc.contributor.author小松, 和人ja
dc.contributor.author塚原, 健治ja
dc.contributor.alternativeTakata, Masayukien
dc.contributor.alternativeMiyoshi, Mitsuruen
dc.contributor.alternativeKohno, Masanorien
dc.contributor.alternativeIto, Masanorien
dc.contributor.alternativeKomatsu, Kazutoen
dc.contributor.alternativeTsukahara, Kenjien
dc.date.accessioned2012-12-20T01:33:17Z-
dc.date.available2012-12-20T01:33:17Z-
dc.date.issued2012-11-
dc.identifier.issn0018-1994-
dc.identifier.urihttp://hdl.handle.net/2433/166349-
dc.description.abstractCase 1 : The patient was a 68-year-old man. Abdominal computed tomography performed during hospitalization for the close observation of a pituitary gland tumor, showed a right renal mass. Percutaneus needle biopsy revealed IgG4-related disease of the kidney. Pituitary gland tumor biopsy also indicated that the lesion was associated with IgG4-related disease. The pancreas did not show abnormalities. The patient was treated with prednisolone, and both renal and pituitary lesions markedly decreased in size. Case 2 : the patient was an 80-year-old man. Right hydronephrosis was observed, and computed tomography showed a right pelvic tumor. Right renal pelvic tumor was diagnosed, and the patient underwent right nephroureterectomy. Pathological examination showed that this tumor was also associated with IgG4-related sclerotic disease. IgG4-related disease tends to occur in multiple organs. This condition should be considered when treating patients with multiple sclerotic diseases. However, in some patients, the disease may be localized to a single site. Further studies are required to elucidate the characteristics of IgG4-related disease.en
dc.format.mimetypeapplication/pdf-
dc.language.isojpn-
dc.publisher泌尿器科紀要刊行会ja
dc.rights許諾条件により本文は2013-12-01に公開ja
dc.subjectIgG4 related systemic diseaseen
dc.subjectRenal tumoren
dc.subjectRenal pelvisen
dc.subject.ndc494.9-
dc.title尿路に発生したIgG4関連硬化性疾患の2例ja
dc.title.alternativeTwo Cases of IgG4-Related Systemic Disease Arising from Urinary Tracten
dc.typedepartmental bulletin paper-
dc.type.niitypeDepartmental Bulletin Paper-
dc.identifier.ncidAN00208315-
dc.identifier.jtitle泌尿器科紀要ja
dc.identifier.volume58-
dc.identifier.issue11-
dc.identifier.spage613-
dc.identifier.epage616-
dc.textversionpublisher-
dc.sortkey04-
dc.address福井赤十字病院腎臓泌尿器科ja
dc.address福井赤十字病院腎臓泌尿器科ja
dc.address福井赤十字病院腎臓泌尿器科ja
dc.address福井赤十字病院腎臓泌尿器科ja
dc.address福井赤十字病院腎臓泌尿器科ja
dc.address福井赤十字病院腎臓泌尿器科ja
dc.startdate.bitstreamsavailable2013-12-01-
dc.address.alternativeThe Department of Nephrology and Urology, Japanese Fukui Red Cross Hospitalen
dc.address.alternativeThe Department of Nephrology and Urology, Japanese Fukui Red Cross Hospitalen
dc.address.alternativeThe Department of Nephrology and Urology, Japanese Fukui Red Cross Hospitalen
dc.address.alternativeThe Department of Nephrology and Urology, Japanese Fukui Red Cross Hospitalen
dc.address.alternativeThe Department of Nephrology and Urology, Japanese Fukui Red Cross Hospitalen
dc.address.alternativeThe Department of Nephrology and Urology, Japanese Fukui Red Cross Hospitalen
dc.identifier.pmid23254786-
dcterms.accessRightsopen access-
dc.identifier.pissn0018-1994-
dc.identifier.jtitle-alternativeActa urologica Japonicala
dc.identifier.jtitle-alternativeHinyokika Kiyoen
出現コレクション:Vol.58 No.11

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