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==Overview==
==Overview==


The most potent risk factor in the development of adrenocortical cancer is [[TP53| TP53 mutation]].
The most potent risk factors in the development of adrenocortical cancer are [[TP53| TP53 mutation]], [[Beckwith-Wiedemann syndrome]] and [[Carney complex]].<ref name="cancergov">National Cancer Institute. Physician Data Query Database 2015.http://www.cancer.gov/types/adrenocortical/patient/adrenocortical-treatment-pdq#section/_1</ref>
==Common Risk Factors==
==Common Risk Factors==
Families with [[Li-Fraumeni syndrome]] (TP53 mutation) have increased risk for adrenocortical cancer.
Families with [[Li-Fraumeni syndrome]] (TP53 mutation), [[Beckwith-Wiedemann syndrome]] and [[Carney complex]] have increased risk for adrenocortical cancer.
 
==References==
==References==
{{Reflist|2}}
{{Reflist|2}}
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{{WH}}

Revision as of 13:57, 26 August 2015

Adrenocortical carcinoma Microchapters

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Ahmad Al Maradni, M.D. [2]

Overview

The most potent risk factors in the development of adrenocortical cancer are TP53 mutation, Beckwith-Wiedemann syndrome and Carney complex.[1]

Common Risk Factors

Families with Li-Fraumeni syndrome (TP53 mutation), Beckwith-Wiedemann syndrome and Carney complex have increased risk for adrenocortical cancer.

References

  1. National Cancer Institute. Physician Data Query Database 2015.http://www.cancer.gov/types/adrenocortical/patient/adrenocortical-treatment-pdq#section/_1

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