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dc.contributor.author服部, 愼一ja
dc.contributor.author麦谷, 荘一ja
dc.contributor.author栗田, 豊ja
dc.contributor.author佐藤, 滋則ja
dc.contributor.author今西, 武志ja
dc.contributor.author春日井, 震ja
dc.contributor.alternativeHattori, Shinichien
dc.contributor.alternativeMugiya, Souichien
dc.contributor.alternativeKurita, Yutakaen
dc.contributor.alternativeSato, Shigenorien
dc.contributor.alternativeImanishi, Takeshien
dc.contributor.alternativeKasugai, Shinen
dc.contributor.transcriptionハットリ, シンイチja-Kana
dc.contributor.transcriptionムギヤ, ソウイチja-Kana
dc.contributor.transcriptionクリタ, ユタカja-Kana
dc.contributor.transcriptionサトウ, シゲノリja-Kana
dc.contributor.transcriptionイマニシ, タケシja-Kana
dc.contributor.transcriptionカスガイ, シンja-Kana
dc.date.accessioned2021-02-05T08:15:39Z-
dc.date.available2021-02-05T08:15:39Z-
dc.date.issued2021-01-31-
dc.identifier.issn0018-1994-
dc.identifier.urihttp://hdl.handle.net/2433/261225-
dc.description.abstractA 70-year-old man complaining of pain in his right leg presented to the Department of Orthopedics in our hospital. X-ray findings revealed calcifications around the left kidney. He was referred to our department for further examination. Computed tomography revealed a tumor 3 cm in diameter with calcifications and an obscure border that was located on the caudal side of the pancreas, anterior to the left iliopsoas muscle and at the left side of the aorta. Magnetic resonance imaging showed that the tumor had comparatively low intensity in diffusion-weighted images and the cell density was not high. The contrast of the tumor by enhanced computed tomography was weak, and we had difficulty judging whether the tumor was benign or malignant. Each tumor marker, immunity factor, and hormone-like catecholamine were within the normal range. We considered the retroperitoneal tumor with calcifications as Castleman disease or tumor of nerve origin. It is believed that most retroperitoneal tumors are malignant. We performed laparoscopic surgery to resect the retroperitoneal tumor. Histopathological diagnosis was a primary retroperitoneal venous malformation. Vascular malformation derived from the retroperitoneum is rare. Furthermore, very few cases of venous malformation in the retroperitoneum have been reported.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2022/02/01に公開ja
dc.subjectVenous malformationen
dc.subjectRetroperitoneal tumoren
dc.subject.ndc494.9-
dc.title後腹膜に発生した静脈奇形の1例ja
dc.title.alternativeA Case of Venous Malformation that Occurred in the Retroperitoneumen
dc.typedepartmental bulletin paper-
dc.type.niitypeDepartmental Bulletin Paper-
dc.identifier.ncidAN00208315-
dc.identifier.jtitle泌尿器科紀要ja
dc.identifier.volume67-
dc.identifier.issue1-
dc.identifier.spage11-
dc.identifier.epage15-
dc.textversionpublisher-
dc.sortkey03-
dc.addressすずかけセントラル病院泌尿器科ja
dc.address浜松とよおか病院ja
dc.addressすずかけセントラル病院泌尿器科ja
dc.addressすずかけセントラル病院泌尿器科ja
dc.address丸山病院泌尿器科ja
dc.addressすずかけセントラル病院泌尿器科ja
dc.address.alternativeThe Department of Urology, Suzukake Central Hospitalen
dc.address.alternativeHamamatsu Toyooka Hospitalen
dc.address.alternativeThe Department of Urology, Suzukake Central Hospitalen
dc.address.alternativeThe Department of Urology, Suzukake Central Hospitalen
dc.address.alternativeThe Department of Urology, Maruyama Hospitalen
dc.address.alternativeThe Department of Urology, Suzukake Central Hospitalen
dc.identifier.pmid33535291-
dc.identifier.selfDOI10.14989/ActaUrolJap_67_1_11-
dcterms.accessRightsopen access-
datacite.date.available2022-02-01-
dc.identifier.pissn0018-1994-
dc.identifier.jtitle-alternativeActa urologica Japonicala
dc.identifier.jtitle-alternativeHinyokika Kiyoen
出現コレクション:Vol.67 No.1

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