Adrenocortical carcinoma epidemiology and demographics: Difference between revisions
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{{Adrenocortical carcinoma}} | {{Adrenocortical carcinoma}} | ||
{{CMG}}; {{AE}} {{RT}} | {{CMG}}; {{AE}} {{RT}}{{AAM}} | ||
==Overview== | |||
==Epidemiology and Demographics== | ==Epidemiology and Demographics== | ||
Adrenocortical carcinoma is a rare | *Adrenocortical carcinoma is a rare [[cancer]], with [[incidence]] of 10-20 per 100,000 population annually.<ref name="DeVita">{{cite book |author=edited by Vincent T. DeVita, Samuel Hellman, Steven A. Rosenberg |title=Cancer: principles & practice of oncology |publisher=Lippincott-Raven |location=Philadelphia |year=2005 |pages=|isbn=0-7817-4865-8 |oclc= |doi=}}</ref> | ||
*Adrenocortical carcinoma has a bimodal distribution by age, with cases clustering in children under 6, and in adults 30-40 years old.<ref name="DeVita"/> | |||
==References== | ==References== | ||
Revision as of 15:41, 25 August 2015
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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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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Raviteja Guddeti, M.B.B.S. [2]Ahmad Al Maradni, M.D. [3]
Overview
Epidemiology and Demographics
- Adrenocortical carcinoma is a rare cancer, with incidence of 10-20 per 100,000 population annually.[1]
- Adrenocortical carcinoma has a bimodal distribution by age, with cases clustering in children under 6, and in adults 30-40 years old.[1]
References
- ↑ 1.0 1.1 edited by Vincent T. DeVita, Samuel Hellman, Steven A. Rosenberg (2005). Cancer: principles & practice of oncology. Philadelphia: Lippincott-Raven. ISBN 0-7817-4865-8.