Adrenocortical adenomas (ACA) are frequently discovered at autopsy. No
wadays, modern radiologic techniques incidentally uncover the usually
silent ACA during lifetime. On the basis of various reports and the re
sults of endocrine tests, i.e. dexamethasone suppression (DST) and CRH
response, we characterize 3 major types of functioning ACA. Type I AC
A (cortisol <100 nmol/l after 1 mg dexamethasone (DXM)) comprises the
majority of the so-called 'nonfunctioning' adrenocortical adenomas. Ho
wever, these adenomas may not be 'truly nonfunctioning' ACA, as their
mean F(MAX)/ACTH(MAX)-ratio after CRH is significantly higher than in
controls without ACA. Also, 19-iodocholesterol adrenal scan has shown
persistent adrenal uptake despite DXM administration in some patients
with normal DST. Type II ACA ('pre-Cushing's') is comparable to the eu
thyroid autonomous adenoma. The results of function tests suggest the
existence of an ACTH-hyperresponsive subtype. Finally, type III ACA ar
e associated with overt hypercortisolism. An ACTH-responsive and an AC
TH-unresponsive form can be characterized. A continuous functional spe
ctrum and the transition between the different types of adenomas is di
scussed.