Adrenocortical Carcinoma with Hypercortisolism.

Abstract:

:Adrenocortical carcinoma (ACC) is a rare and aggressive tumor. ACC may be associated with different syndromes of hormone excess, most frequently Cushing's syndrome with or without hypersecretion of androgens. Recent data suggest that cortisol excess is a negative prognostic factor in advanced and localized ACC. Surgery with radical intent, when feasible, is the most effective treatment for ACC with hypercortisolism. Mitotane is the medical treatment of choice, both postoperatively and in inoperable or metastatic cases. Because of its slow onset of action, combination with other antisecretory agents (ie, metyrapone) is helpful to achieve more rapid and effective control of hypercortisolism.

authors

Puglisi S,Perotti P,Pia A,Reimondo G,Terzolo M

doi

10.1016/j.ecl.2018.02.003

subject

Has Abstract

pub_date

2018-06-01 00:00:00

pages

395-407

issue

2

eissn

0889-8529

issn

1558-4410

pii

S0889-8529(18)30011-2

journal_volume

47

pub_type

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