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dc.contributor.author壽美, 周平ja
dc.contributor.author國保, 昌紀ja
dc.contributor.author石橋, 克夫ja
dc.contributor.author山内, 民男ja
dc.contributor.author鷲塚, 誠ja
dc.contributor.author河合, 恒雄ja
dc.contributor.alternativeSUMI, Shuheien
dc.contributor.alternativeKOKUHO, Masanorien
dc.contributor.alternativeISHIBASHI, Yoshioen
dc.contributor.alternativeYAMAUCHI, Tamioen
dc.contributor.alternativeWASHIZUKA, Makotoen
dc.contributor.alternativeKAWAI, Tsuneoen
dc.date.accessioned2010-06-02T02:48:00Z-
dc.date.available2010-06-02T02:48:00Z-
dc.date.issued1988-05-
dc.identifier.issn0018-1994-
dc.identifier.urihttp://hdl.handle.net/2433/119568-
dc.description.abstractWe report 2 cases of adrenal myelolipoma which were suspected preoperatively and confirmed by surgical resection. As with most cases previously reported, the lesions were found in obese, middle-aged persons. Laboratory tests of adrenal function revealed values within the normal level. Excretory urography showed radiolucent masses in the suprarenal area displacing the kidney inferiorly. Computerized tomography revealed well-defined masses consisting of fat density areas and higher density areas. Ultrasonography demonstrated hyperechoic, heterogeneous tumors. The tumors were shown to be hypovascular and adrenal in origin on the angiogram. An operation was performed because of complaint of flank pain in the first case and hypertension associated with elevated plasma renin activity in the second case. The pathological study disclosed typical adrenal myelolipoma with a mixture of hematopoietic and adipose tissue. Adrenal myelolipoma is clinically unusual and only 41 cases with premortem diagnosis have been reported in English literature. We herein report the 14th and 15th cases in Japan. As computerized tomography and ultrasonography become more widely used, we believe that the number of cases difficult to differentiate from a malignancy will increase.en
dc.format.mimetypeapplication/pdf-
dc.language.isojpn-
dc.publisher泌尿器科紀要刊行会ja
dc.subjectAdrenal myelolipomaen
dc.subjectSuprarenal massen
dc.subject.ndc494.9-
dc.title副腎骨髄脂肪腫の2例ja
dc.title.alternativeAdrenal myelolipoma: two case reportsen
dc.typedepartmental bulletin paper-
dc.type.niitypeDepartmental Bulletin Paper-
dc.identifier.ncidAN00208315-
dc.identifier.jtitle泌尿器科紀要ja
dc.identifier.volume34-
dc.identifier.issue5-
dc.identifier.spage855-
dc.identifier.epage861-
dc.textversionpublisher-
dc.sortkey16-
dc.address癌研究会付属病院泌尿器科ja
dc.address癌研究会付属病院泌尿器科ja
dc.address癌研究会付属病院泌尿器科ja
dc.address癌研究会付属病院泌尿器科ja
dc.address癌研究会付属病院泌尿器科ja
dc.address癌研究会付属病院泌尿器科ja
dc.address.alternativethe Department of Urology, Cancer Institute Hospitalen
dc.address.alternativethe Department of Urology, Cancer Institute Hospitalen
dc.address.alternativethe Department of Urology, Cancer Institute Hospitalen
dc.address.alternativethe Department of Urology, Cancer Institute Hospitalen
dc.address.alternativethe Department of Urology, Cancer Institute Hospitalen
dc.address.alternativethe Department of Urology, Cancer Institute Hospitalen
dc.identifier.pmid3051940-
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.34 No.5

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