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dc.contributor.author風間, 泰蔵ja
dc.contributor.author保田, 賢司ja
dc.contributor.author木村, 仁美ja
dc.contributor.alternativeKazama, Taizoen
dc.contributor.alternativeYasuda, Kenjien
dc.contributor.alternativeKimura, Hitomien
dc.contributor.transcriptionカザマ, タイゾウja-Kana
dc.contributor.transcriptionヤスダ, ケンジja-Kana
dc.contributor.transcriptionキムラ, ヒトミja-Kana
dc.date.accessioned2019-05-09T10:19:42Z-
dc.date.available2019-05-09T10:19:42Z-
dc.date.issued2019-02-28-
dc.identifier.issn0018-1994-
dc.identifier.urihttp://hdl.handle.net/2433/241224-
dc.description.abstractA 41-year-old male with the chief complaint of infertility was referred to our hospital. He presented withmild erectile dysfunction and reduced shaving frequency. Semen analysis indicated a decreased semen volume in addition to a low sperm count and motility. Hormone evaluation revealed the following details : follicle stimulating hormone (FSH) 1.7 mIU/ml (range 2.0-8.3 mIU/ml), luteinizing hormone (LH) 0.9 mIU/ml (range 0.8-5.7 mIU/ml), testosterone 86.6 ng/dl (range 225.0-1, 039 ng/dl), and prolactin (PRL) 242.0 ng/ml (range 3.6-12.8 ng/ml). Magnetic resonance imaging (MRI) of the patient's head showed empty sella turcica. He was diagnosed with acquired hypogonadotropic hypogonadism due to hyperprolactinemia. We suspected that the hyperprolactinemia was due to the pituitary lesion, although the possibility of coexisting pituitary microadenoma could not be discarded. Based on the diagnosis, cabergoline therapy was started. Four months after initiation of cabergoline therapy, the patient's hormone levels and semen parameters normalized, followed by improvement in his clinical symptoms. Furthermore, his wife spontaneously conceived.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2020/03/01に公開ja
dc.subjectMale infertilityen
dc.subjectHyperprolactinemiaen
dc.subjectEmpty sellaen
dc.subject.ndc494.9-
dc.titleトルコ鞍空洞症に伴う高プロラクチン血症が原因と考えられた男性不妊症の1例ja
dc.title.alternativeInfertility Due to Hyperprolactinemia in Empty Sella : A Case Reporten
dc.typedepartmental bulletin paper-
dc.type.niitypeDepartmental Bulletin Paper-
dc.identifier.ncidAN00208315-
dc.identifier.jtitle泌尿器科紀要ja
dc.identifier.volume65-
dc.identifier.issue2-
dc.identifier.spage55-
dc.identifier.epage59-
dc.textversionpublisher-
dc.sortkey05-
dc.address富山県済生会富山病院泌尿器科ja
dc.address富山県済生会富山病院泌尿器科ja
dc.address富山県済生会富山病院泌尿器科ja
dc.address.alternativeThe Department of Urology, Saiseikai Toyama Hospitalen
dc.address.alternativeThe Department of Urology, Saiseikai Toyama Hospitalen
dc.address.alternativeThe Department of Urology, Saiseikai Toyama Hospitalen
dc.identifier.pmid31067844-
dc.identifier.selfDOI10.14989/ActaUrolJap_65_2_55-
dcterms.accessRightsopen access-
datacite.date.available2020-03-01-
dc.identifier.pissn0018-1994-
dc.identifier.jtitle-alternativeActa urologica Japonicala
dc.identifier.jtitle-alternativeHinyokika Kiyoen
出現コレクション:Vol.65 No.2

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