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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
|
pubmed:dateCreated |
1990-12-21
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pubmed:abstractText |
Although 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.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0022-5347
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
144
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1454-6
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:2231941-Adrenal Cortex Neoplasms,
pubmed-meshheading:2231941-Aged,
pubmed-meshheading:2231941-Carcinoma,
pubmed-meshheading:2231941-Humans,
pubmed-meshheading:2231941-Hyperaldosteronism,
pubmed-meshheading:2231941-Karyotyping,
pubmed-meshheading:2231941-Klinefelter Syndrome,
pubmed-meshheading:2231941-Male,
pubmed-meshheading:2231941-Mosaicism
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pubmed:year |
1990
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pubmed:articleTitle |
Isolated primary aldosteronism in a patient with adrenal carcinoma and XY/XXY mosaic Klinefelter's syndrome.
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pubmed:affiliation |
Department of Nephrology, Hospital Ramón y Cajal, Madrid, Spain.
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pubmed:publicationType |
Journal Article,
Case Reports
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