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dc.contributor.authorBabiker, Tarig
dc.contributor.authorKyrodimou, Efstathia
dc.contributor.authorBerney, Daniel M
dc.contributor.authorGurnell, Mark
dc.contributor.authorDrake, William M
dc.contributor.authorBrooke, Antonia
dc.date.accessioned2018-11-14T00:30:55Z
dc.date.available2018-11-14T00:30:55Z
dc.date.issued2017-11
dc.identifier.issn2050-0904
dc.identifier.urihttps://www.repository.cam.ac.uk/handle/1810/285035
dc.description.abstractA 60-year-old man with a pre-existing stable sacrococcygeal teratoma developed acromegaly, ectopic Cushing's syndrome, and 5HIAA secretion. To our knowledge, this represents the first reported case of ACTH and serotonin secretion, and likely GHRH or GH cosecretion, from a sacrococcygeal teratoma in an adult.
dc.format.mediumElectronic-eCollection
dc.languageeng
dc.publisherWiley
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleAcromegaly and Cushing's syndrome caused by a neuroendocrine tumor arising within a sacrococcygeal teratoma.
dc.typeArticle
prism.endingPage1771
prism.issueIdentifier11
prism.publicationDate2017
prism.publicationNameClin Case Rep
prism.startingPage1768
prism.volume5
dc.identifier.doi10.17863/CAM.32405
dcterms.dateAccepted2017-07-20
rioxxterms.versionofrecord10.1002/ccr3.1148
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.licenseref.startdate2017-11
dc.contributor.orcidBabiker, Tarig [0000-0001-8759-8516]
dc.contributor.orcidGurnell, Mark [0000-0001-5745-6832]
dc.identifier.eissn2050-0904
rioxxterms.typeJournal Article/Review
cam.issuedOnline2017-09-14


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Attribution 4.0 International
Except where otherwise noted, this item's licence is described as Attribution 4.0 International