G. Osella et al., ENDOCRINE EVALUATION OF INCIDENTALLY DISCOVERED ADRENAL MASSES (INCIDENTALOMAS), The Journal of clinical endocrinology and metabolism, 79(6), 1994, pp. 1532-1539
Since 1989, 45 patients [pts; 26 females and 19 males, aged 19-79 yr (
median, 58)] bearing incidentally discovered adrenal masses were studi
ed. The aim of the study was to verify the prevalence of hormone activ
ity in clinically silent adrenal masses. Endocrine work-up included de
termination of urinary catecholamines and their metabolites, measureme
nt of PRA and aldosterone levels in clino- and orthostatic posture, an
d basal and dynamic [dexamethasone (dex) suppression and ovine CRH sti
mulation] evaluation of hypothalamic-pituitary-adrenal axis. The most
frequent finding was the reduction of dehydroepiandrosterone sulfate (
DHEA-S) levels below the third percentile of controls in 19 (42%) pts.
DHEA-S levels were significantly lower in pts than in controls [68 (r
ange, 5-1000) us. 208 (34-326) mu g/dL; 1.8 (0.1-27.1) us. 5.6 (0.9-8.
8) mu mol/L; P < 0.001]. Three pts (7%) had high 24-h mean serum corti
sol levels, and 6 (14%) had blunted day-night amplitude of cortisol rh
ythm. Defective dex suppressibility was found in 15% of pts vs. 8% of
controls (P < 0.05). ACTH and cortisol responses to ovine CRH did not
significantly differ between pts and controls, although blunted ACTH r
esponses were found in 22% of the cases. The above-mentioned endocrine
alterations could be accounted for by autonomous cortisol secretion b
y the adrenal nodule at a rate not sufficient to give clinical express
ion, but able to inhibit to some extent the hypothalamic-pituitary-adr
enal axis. These results indicate that silent cortisol hypersecretion
is frequently observed in pts with adrenal incidentaloma even if progr
ession to overt Cushing's syndrome seems unlikely. Indeed, the size of
the mass and the hormone pattern remained substantially unchanged in
9 pts followed up for 12 months. From merely a cost/benefit ratio, the
evaluation of DHEA-S levels and dex suppression has sufficient sensit
ivity to identify the occurrence of silent hypercortisolism.