ENDOCRINE EVALUATION OF INCIDENTALLY DISCOVERED ADRENAL MASSES (INCIDENTALOMAS)

Citation
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
Citations number
49
Categorie Soggetti
Endocrynology & Metabolism
ISSN journal
0021972X
Volume
79
Issue
6
Year of publication
1994
Pages
1532 - 1539
Database
ISI
SICI code
0021-972X(1994)79:6<1532:EEOIDA>2.0.ZU;2-4
Abstract
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.