Management of adrenocortical carcinoma

11Citations
Citations of this article
54Readers
Mendeley users who have this article in their library.

Abstract

Adrenocortical carcinomas (ACCs) are rare tumors that arise from the cortex of the adrenal gland with an incidence 1 to 2 per million. The rarity of this tumor translates into a paucity of experience in managing patients in most medical centers. Because clinical series are small and prospective evaluation of treatment strategies is limited, the current state of knowledge is strongly influenced by expert consensus opinion from a few medical centers specializing in ACCs. This article describes the basic diagnostic and prognostic issues in adrenal cancer management, and presents detailed rationales for therapeutic management. © Journal of the National Comprehensive Cancer Network.

Cite

CITATION STYLE

APA

Strosberg, J. R., Hammer, G. D., & Doherty, G. M. (2009). Management of adrenocortical carcinoma. JNCCN Journal of the National Comprehensive Cancer Network, 7(7), 752–759. https://doi.org/10.6004/jnccn.2009.0051

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free