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Primary hyperaldosteronism caused by adrenocortical carcinoma

dc.contributor.authorSussman, Craig R.en_US
dc.contributor.authorPage, David L.en_US
dc.contributor.authorScott, H. Williamen_US
dc.contributor.authorLloyd, Ricardo V.en_US
dc.contributor.authorThompson, Norman W.en_US
dc.contributor.authorGross, Milton D.en_US
dc.date.accessioned2006-09-08T19:04:52Z
dc.date.available2006-09-08T19:04:52Z
dc.date.issued1986-08en_US
dc.identifier.citationScott, H. William; Sussman, Craig R.; Page, David L.; Thompson, Norman W.; Gross, Milton D.; Lloyd, Ricardo; (1986). "Primary hyperaldosteronism caused by adrenocortical carcinoma." World Journal of Surgery 10(4): 646-652. <http://hdl.handle.net/2027.42/41275>en_US
dc.identifier.issn0364-2313en_US
dc.identifier.issn1432-2323en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/41275
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=3751090&dopt=citationen_US
dc.description.abstractSince the syndrome of primary hyperaldosteronism was described by Jerome Conn in 1955, over 300 patients with this disorder have been identified in the medical centers of Vanderbilt University and the University of Michigan. The most frequent cause of this endocrinopathy has been a solitary adenoma of the adrenal cortex (72%); bilateral adrenocortical hyperplasia has been the cause of primary hyperaldosteronism in 27% of cases; less frequently, the cause has been multiple and/or bilateral adenomas (1%). During the last 4 years in these 2 medical centers, we have encountered 3 patients who have had biochemically proven primary hyperaldosteronism due to adrenocortical carcinoma. Each of these unusual cases is summarized with review of the recent literature . Depuis que le syndrome d'hyperaldostéronisme primitif a été décrit par Jerôme Conn en 1955 plus de 300 sujets qui en étaient victimes ont été identifiés à la Vanderbilt University de Nashville et à l'University of Michigan de Ann Arbor. La cause la plus fréquente de cette endocrinopathie répond à un adénome solitaire de la cortico-surrénale (72%) alors que l'hyperplasie corticale des 2 surrénales est plus rarement à son origine (27%), les adénomes multiples et/ou bilatéraux étant rarissimes (1%). Au cours des 4 dernières années 3 cas d'hyperaldosteronisme dû à un cancer de la cortico-surrénale ont été observés dans les 2 centres. Chacun de ces cas exceptionnels est exposé cependant que la littérature récente concernant l'hyperalderosteronisme est analysée. Desde la descripción del síndrome de hiperaldosteronismo primario por Jeremo Conn en 1955, más de 300 pacientes con esta entidad han sido identificados en nuestros 2 centros médicos, la Universidad de Vanderbilt (Nashville) y la Universidad de Michigan (Ann Arbor). La causa más frecuente de esta endocrinopatía ha sido el adenoma solitario de la corteza suprarrenal (72%); la hiperplasia adrenocortical bilateral ha sido la causa del hiperaldosteronismo primario en 27% de los casos; con menor frecuencia se han presentado los adenomas multiples y/o bilaterales (1%). En los 4 últimos años hemos encontrado 3 pacientes con hiperaldosteronismo primario comprobado bioquímicamente producido por carcinoma adrenocortical. Se presenta cada uno de estos casos poco usuales junto con una revisión de la literatura reciente.en_US
dc.format.extent1988078 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlag; Société Internationale de Chirurgieen_US
dc.subject.otherTraumatic Surgeryen_US
dc.subject.otherCardiac Surgeryen_US
dc.subject.otherThoracic Surgeryen_US
dc.subject.otherGeneral Surgeryen_US
dc.subject.otherAbdominal Surgeryen_US
dc.subject.otherMedicine & Public Healthen_US
dc.subject.otherVascular Surgeryen_US
dc.titlePrimary hyperaldosteronism caused by adrenocortical carcinomaen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelSurgery and Anesthesiologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartments of Surgery, Pathology, and Nuclear Medicine, Vanderbilt University, Nashville, Tennessee; University of Michigan, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDepartments of Surgery, Pathology, and Nuclear Medicine, Vanderbilt University, Nashville, Tennessee; University of Michigan, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDepartments of Surgery, Pathology, and Nuclear Medicine, Vanderbilt University, Nashville, Tennessee; University of Michigan, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDepartments of Surgery, Pathology, and Nuclear Medicine, Vanderbilt University, Nashville, Tennessee; University of Michigan, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDepartments of Surgery, Pathology, and Nuclear Medicine, Vanderbilt University, Nashville, Tennessee; University of Michigan, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDepartments of Surgery, Pathology, and Nuclear Medicine, Vanderbilt University, Nashville, Tennessee; University of Michigan, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid3751090en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/41275/1/268_2005_Article_BF01655546.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF01655546en_US
dc.identifier.sourceWorld Journal of Surgeryen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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