All patients with suspected adrenocortical carcinoma should be carefully evaluated for signs and symptoms of hormonal syndromes.
12.
Mir-210 has been suggested as a useful biomarker to distinguish adrenocortical carcinoma from adrenocortical adenoma.
13.
Mir-210 has been suggested as a useful biomarker to distinguish adrenocortical carcinoma from adrenocortical adenoma.
14.
Cerebral cavernomas and massive, macronodular adrenocortical disease have also been reported in association with this syndrome.
15.
Bilateral primary hyperaldosteronism due to hyperplasia of the zona glomerulosa or metastasized adrenocortical adenocarcinoma should be treated medically.
16.
The pituitary-adrenocortical and pituitary-gonadal systems are thought to affect readiness or potentiation for anger responding.
17.
The synthesis of adrenocortical steroid hormones involves a chain of oxidation-reduction reactions catalyzed by a series of enzymes.
18.
Most of the adrenocortical adenomas are less than 2 cm in greatest dimension and less than 50 gram in weight.
19.
Grossly, adrenocortical adenomas are encapsulated, well-circumscribed, solitary tumors with solid, homogeneous yellow-cut surface.
20.
The ACTH stimulation test does not distinguish between primary adrenal insufficiency and secondary insufficiency or adrenocortical destruction caused by mitotane overdose.
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