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pubmed-article:2231941pubmed:abstractTextAlthough breast cancer, germ cell tumors and other neoplasms are known to occur in patients with Klinefelter's syndrome, adrenal carcinoma has not yet been reported in such patients. We describe a rare case of severe primary aldosteronism as the unique manifestation of a large adrenocortical carcinoma in a patient with Klinefelter's syndrome. Complete biological and hormonal evaluation was performed. Surgical treatment was successful and the patient remained asymptomatic with normal biological and hormonal values after 1 year of followup.lld:pubmed
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pubmed-article:2231941pubmed:issn0022-5347lld:pubmed
pubmed-article:2231941pubmed:authorpubmed-author:PascualJJlld:pubmed
pubmed-article:2231941pubmed:authorpubmed-author:LiañoFFlld:pubmed
pubmed-article:2231941pubmed:authorpubmed-author:OrtuñoJJlld:pubmed
pubmed-article:2231941pubmed:authorpubmed-author:HerreroJ AJAlld:pubmed
pubmed-article:2231941pubmed:authorpubmed-author:SalvadorJ LJLlld:pubmed
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pubmed-article:2231941pubmed:dateRevised2004-11-17lld:pubmed
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pubmed-article:2231941pubmed:year1990lld:pubmed
pubmed-article:2231941pubmed:articleTitleIsolated primary aldosteronism in a patient with adrenal carcinoma and XY/XXY mosaic Klinefelter's syndrome.lld:pubmed
pubmed-article:2231941pubmed:affiliationDepartment of Nephrology, Hospital Ramón y Cajal, Madrid, Spain.lld:pubmed
pubmed-article:2231941pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:2231941pubmed:publicationTypeCase Reportslld:pubmed