Adrenocortical carcinoma pathophysiology: Difference between revisions
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==Overview== | ==Overview== | ||
Adrenocortical carcinoma may be linked to a cancer syndrome that is passed down through families (inherited). | |||
Adrenocortical carcinoma can produce the hormones [[cortisol]], [[aldosterone]], [[estrogen]], or [[testosterone]], as well as other hormones. In women the tumor often releases these hormones, which can lead to male characteristics. | |||
Studies suggest that [[mutations]] of the tumor suppressor genes TP53 and TP57 may be contributing factors for development of [[Adrenocortical carcinoma]]. | |||
==References== | ==References== | ||
Revision as of 06:46, 29 July 2012
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Adrenocortical carcinoma Microchapters |
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Differentiating Adrenocortical carcinoma from other Diseases |
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Diagnosis |
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Treatment |
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Case Study |
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Adrenocortical carcinoma pathophysiology On the Web |
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American Roentgen Ray Society Images of Adrenocortical carcinoma pathophysiology |
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Risk calculators and risk factors for Adrenocortical carcinoma pathophysiology |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Adrenocortical carcinoma may be linked to a cancer syndrome that is passed down through families (inherited).
Adrenocortical carcinoma can produce the hormones cortisol, aldosterone, estrogen, or testosterone, as well as other hormones. In women the tumor often releases these hormones, which can lead to male characteristics.
Studies suggest that mutations of the tumor suppressor genes TP53 and TP57 may be contributing factors for development of Adrenocortical carcinoma.