Adrenocortical carcinoma epidemiology and demographics: Difference between revisions
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*Adrenocortical carcinoma is a rare [[cancer]], with [[incidence]] of 0.1-0.2 per 100,000 individuals annually. | *Adrenocortical carcinoma is a rare [[cancer]], with [[incidence]] of 0.1-0.2 per 100,000 individuals annually. | ||
===Age=== | ===Age=== | ||
*Adrenocortical carcinoma has a [[bimodal distribution]] by age, with cases clustering in children under 6, and in adults 30-40 years old. | *Adrenocortical carcinoma has a [[bimodal distribution]] by age, with cases clustering in children under 6, and in adults 30-40 years old. | ||
==References== | ==References== |
Revision as of 21:22, 27 August 2015
Adrenocortical carcinoma Microchapters |
Differentiating Adrenocortical carcinoma from other Diseases |
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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
Adrenocortical carcinoma is a rare cancer that tends to affect children and young adults.
Epidemiology and Demographics
Incidence
- Adrenocortical carcinoma is a rare cancer, with incidence of 0.1-0.2 per 100,000 individuals annually.
Age
- Adrenocortical carcinoma has a bimodal distribution by age, with cases clustering in children under 6, and in adults 30-40 years old.