Adrenocortical carcinoma pathophysiology: Difference between revisions
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{{Adrenocortical carcinoma}} | {{Adrenocortical carcinoma}} | ||
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==Overview== | ==Overview== | ||
==Pathophysiology== | |||
Adrenocortical carcinoma may be linked to a cancer syndrome that is passed down through families (inherited). | Adrenocortical carcinoma may be linked to a cancer syndrome that is passed down through families (inherited). | ||
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Revision as of 17:30, 19 September 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 |
Please help WikiDoc by adding more content here. It's easy! Click here to learn about editing. Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Raviteja Guddeti, M.B.B.S. [2]
Overview
Pathophysiology
Adrenocortical carcinoma may be linked to a cancer syndrome that is passed down through families (inherited).
This tumor 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 might also be possible contributing factors for the development of Adrenocortical carcinoma.