An adrenal incidentaloma is now established as a common endocrine diagnosis that
requires a multidisciplinary approach for effective management. The majority of patients can …

Adrenal tumors are commonly discovered incidentally on cross-sectional abdominal
imaging performed for reasons other than adrenal mass. Incidence of adrenal tumors …

Adrenal incidentalomas are adrenal masses detected on imaging performed for reasons
other than suspected adrenal disease. In most cases, adrenal incidentalomas are …

Two different primary malignancies can arise from the adrenal gland: adrenocortical
carcinoma (ACC) from the adrenal cortex and malignant phaeochromocytoma from the …

Adrenocortical carcinoma (ACC) is a rare and in most cases steroid hormone-producing
tumor with variable prognosis. The purpose of these guidelines is to provide clinicians with …

Steroid biosynthesis and metabolism are reflected by the serum steroid metabolome and, in
even more detail, by the 24-hour urine steroid metabolome, which can provide unique …

Adrenocortical carcinoma (ACC) is an aggressive and rare neoplasm that originates in the
cortex of the adrenal gland. The disease is associated with heterogeneous but mostly poor …

Background Adrenocortical carcinoma (ACC) is an aggressive and rare malignant tumor
and is prone to local invasion and metastasis. And, overexpressed Centromere Protein F …

Adrenocortical carcinoma is a rare malignancy with an annual worldwide incidence of 1–2
cases per 1 million and a 5-year survival rate of< 60%. Although adrenocortical carcinoma is …

Objective Current workup for the pre-operative distinction between frequent adrenocortical
adenomas (ACAs) and rare but aggressive adrenocortical carcinomas (ACCs) combines …