Identifying and Treating Hypercortisolism in Adrenal Incidentalomas

Article Figures & Data

Figures

  • Figure 1.

    Mutation of ARMC5 Resulting in BMAH in a Large Family

    CT=computed tomography; DST=dexamethasone suppression test; PMAH=primary macronodular adrenal hyperplasia.Reproduced from Alencar GA et al. ARMC5 mutations are a frequent cause of primary macronodular adrenal hyperplasia. J Clin Endocrinol Metab. 2014;99(8):E1501–E1509. With permission from The Endocrine Society.
  • Figure 2.

    All-Cause Mortality Among Patients With Adrenal Incidentalomas

    Reproduced from Di Dalmazi G et al. Cardiovascular events and mortality in patients with adrenal incidentalomas that are either non-secreting or associated with intermediate phenotype or subclinical Cushing's syndrome: a 15-year retrospective study. Lancet Diabetes Endocrinol. 2014;2:396–405. With permission from Elsevier.
  • Figure 3.

    Cardiovascular Risk Factors Among Patients With Adrenal Incidentalomas

    Reproduced with permission from M. Debono, MD. Adapted from Di Dalmazi et al. Progressively increased patterns of subclinical cortisol hypersecretion in adrenal incidentalomas differently predict major metabolic and cardiovascular outcomes: a large cross-sectional study. Eur J Endocrinol. 2012;166:669–677.