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dc.contributor.author市川, 智彦ja
dc.contributor.author始関, 吉生ja
dc.contributor.author角谷, 秀典ja
dc.contributor.author井坂, 茂夫ja
dc.contributor.author島崎, 淳ja
dc.contributor.author寺野, 隆ja
dc.contributor.author小林, 弘一ja
dc.contributor.author山本, 和男ja
dc.contributor.author田村, 泰ja
dc.contributor.author古田, 尚ja
dc.contributor.author松嵜, 理ja
dc.contributor.alternativeIchikawa, Tomohikoen
dc.contributor.alternativeShiseki, Yoshioen
dc.contributor.alternativeSumiya, Hidenorien
dc.contributor.alternativeIsaka, Shigeoen
dc.contributor.alternativeShimazaki, Junen
dc.contributor.alternativeTerano, Takashien
dc.contributor.alternativeKobayashi, Hirokazuen
dc.contributor.alternativeYamamoto, Kazuoen
dc.contributor.alternativeTamura, Yasushien
dc.contributor.alternativeYoshida, Shouen
dc.contributor.alternativeMatsuzaki, Osamuen
dc.date.accessioned2010-06-01T02:55:56Z-
dc.date.available2010-06-01T02:55:56Z-
dc.date.issued1992-09-
dc.identifier.issn0018-1994-
dc.identifier.urihttp://hdl.handle.net/2433/117652-
dc.description.abstractA 66-year-old female was admitted to Chiba University Hospital for the evaluation of a left adrenal mass which was incidentally discovered by computerized tomography. The patient had no clinical signs of Cushing's syndrome. Although the plasma ACTH level was suppressed, serum cortisol and urinary 17-OHCS levels were normal. Serum cortisol was not suppressed by dexamethasone and loss of diurnal rhythm of cortisol was observed. Uptake of 131I-aldosterone in the left adrenal gland was noted, but no accumulation was observed in the right one. Left adrenalectomy was performed. The tumor resected was 20 x 22 x 26 mm in size. Pathological diagnosis was adreno-cortical adenoma. Whether slight abnormality of adrenocortical function without clinical symptoms observed in the present case would develop into a clinically typical Cushing's syndrome remains to be solved.en
dc.format.mimetypeapplication/pdf-
dc.language.isojpn-
dc.publisher泌尿器科紀要刊行会ja
dc.subjectIncidentalomaen
dc.subjectAdrenocortical adenomaen
dc.subjectPre-Cushing's syndromeen
dc.subject.ndc494.9-
dc.titlePre-Cushing症候群の1例ja
dc.title.alternativeA case of pre-Cushing's syndromeen
dc.typedepartmental bulletin paper-
dc.type.niitypeDepartmental Bulletin Paper-
dc.identifier.ncidAN00208315-
dc.identifier.jtitle泌尿器科紀要ja
dc.identifier.volume38-
dc.identifier.issue9-
dc.identifier.spage1031-
dc.identifier.epage1035-
dc.textversionpublisher-
dc.sortkey08-
dc.address千葉大学医学部泌尿器科学教室ja
dc.address千葉大学医学部泌尿器科学教室ja
dc.address千葉大学医学部泌尿器科学教室ja
dc.address千葉大学医学部泌尿器科学教室ja
dc.address千葉大学医学部泌尿器科学教室ja
dc.address千葉大学医学部第二内科学教室ja
dc.address千葉大学医学部第二内科学教室ja
dc.address千葉大学医学部第二内科学教室ja
dc.address千葉大学医学部第二内科学教室ja
dc.address千葉大学医学部第二内科学教室ja
dc.address千葉県がんセンター臨床病理部ja
dc.address.alternativethe Department of Urology, School of Medicine, Chiba Universityen
dc.address.alternativethe Department of Urology, School of Medicine, Chiba Universityen
dc.address.alternativethe Department of Urology, School of Medicine, Chiba Universityen
dc.address.alternativethe Department of Urology, School of Medicine, Chiba Universityen
dc.address.alternativethe Department of Urology, School of Medicine, Chiba Universityen
dc.address.alternativethe2nd Department of Internal Medicine, School of Medicine, Chiba Universityen
dc.address.alternativethe2nd Department of Internal Medicine, School of Medicine, Chiba Universityen
dc.address.alternativethe2nd Department of Internal Medicine, School of Medicine, Chiba Universityen
dc.address.alternativethe2nd Department of Internal Medicine, School of Medicine, Chiba Universityen
dc.address.alternativethe2nd Department of Internal Medicine, School of Medicine, Chiba Universityen
dc.address.alternativethe Division of Surgical Pathology, Chiba Cancer Center Hospitalen
dc.identifier.pmid1329452-
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.38 No.9

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