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dc.contributor.author黒部, 匡広ja
dc.contributor.author小島, 崇宏ja
dc.contributor.author内田, 将央ja
dc.contributor.author宮川, 友明ja
dc.contributor.author堤, 雅一ja
dc.contributor.author杉田, 真太朗ja
dc.contributor.alternativeKurobe, Masahiroen
dc.contributor.alternativeKojima, Takahiroen
dc.contributor.alternativeUchida, Masahiroen
dc.contributor.alternativeMiyagawa, Tomoakien
dc.contributor.alternativeTsutsumi, Masakazuen
dc.contributor.alternativeSugita, Shintaroen
dc.date.accessioned2012-08-16T01:55:15Z-
dc.date.available2012-08-16T01:55:15Z-
dc.date.issued2012-07-
dc.identifier.issn0018-1994-
dc.identifier.urihttp://hdl.handle.net/2433/159085-
dc.description.abstractUreteral endometriosis is a rare but important clinical problem that requires early detection and treatment. The urinary tract is affected in approximately 2% of women with endometriosis. Even though the bladder is the most frequent urinary tract organ affected in these patients, the ureter is also affected in 10-40% of the cases, thus requiring immediate clinical attention. The majority of endometrial lesions is typically located in the lower segment of the ureter and is often difficult to differentiate between endometriosis and malignancy. Ureteral endmetriosis should be considered for women with hydronephrosis. In this report we present one clinical case of mixed-type ureteral endometriosis. A 37-year-old woman was referred to our hospital due to left hydronephrosis. Contrast-enhanced CT scan confirmed left hydronephrosis and also showed a solid mass at the left lower ureter. Retrograde pyelography revealed stenosis of the left lower ureter and Renogram revealed severely impaired renal function. Laparoscopic nephroureterectomy was performed. Pathologically, mixed-type endometriosis of the left ureter was diagnosed.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2013-08-01に公開ja
dc.subjectUreteral endometriosisen
dc.subject.ndc494.9-
dc.title混合性尿管子宮内膜症の1例と本邦文献例の検討ja
dc.title.alternativeMixed Type Ureteral Endometriosis : A Case Report and a Review of the Japanese Literatureen
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.issue7-
dc.identifier.spage329-
dc.identifier.epage333-
dc.textversionpublisher-
dc.sortkey04-
dc.address株式会社日立製作所日立総合病院泌尿器科ja
dc.address株式会社日立製作所日立総合病院泌尿器科ja
dc.address株式会社日立製作所日立総合病院泌尿器科ja
dc.address株式会社日立製作所日立総合病院泌尿器科ja
dc.address株式会社日立製作所日立総合病院泌尿器科ja
dc.address株式会社日立製作所日立総合病院病理科ja
dc.startdate.bitstreamsavailable2013-08-01-
dc.address.alternativeThe Department of Urology, Hitachi General Hospitalen
dc.address.alternativeThe Department of Urology, Hitachi General Hospitalen
dc.address.alternativeThe Department of Urology, Hitachi General Hospitalen
dc.address.alternativeThe Department of Urology, Hitachi General Hospitalen
dc.address.alternativeThe Department of Urology, Hitachi General Hospitalen
dc.address.alternativeThe Department of Pathology, Hitachi General Hospitalen
dc.identifier.pmid22895128-
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.7

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