R. Bellantone et al., ADRENAL CYSTIC LESIONS - REPORT OF 12 SURGICALLY TREATED CASES AND REVIEW OF THE LITERATURE, Journal of endocrinological investigation, 21(2), 1998, pp. 109-114
Adrenal cysts are rare (0,064%-0,18% in autopsy series) and less than
500 cases have been reported in the western literature. Incidental dia
gnosis of adrenal cysts, however, is reported with increasing rates. W
e observed 12 patients with adrenal cyst. Each of them had a careful l
aboratory and instrumental evaluation; all the patients were operated.
In our series about 67% of the patients were symptomatic (6 patients
with abdominal pain, 1 with palpable mass, 1 with hemorrhagic shock).
No biochemical alteration was observed. Conversely we observed an unus
ual subclinically hyperfunctioning cystic adenoma, potentially progres
sive to a clinically recognizable endocrine syndrome. US, CT and MRI h
ad a sensitivity of 66,7%, 80% and 100% respectively. Adrenalectomy wa
s performed in all patients. The pathological findings were: 1 epithel
ial cyst (cystic adenoma), 2 endothelial cysts (vascular cystic ectasi
a with adenomatous adrenocortical hyperplasia and 1 vascular cyst) and
9 pseudocysts. On the basis of these results, we conclude that a care
ful hormonal, morpho-functional and instrumental evaluation is indicat
ed in all adrenal cysts, even if the available diagnostic procedures,
even when combined, cannot always define their nature. Surgical excisi
on, when possible by laparoscopic approach, is indicated in presence o
f symptoms, endocrine abnormalities (even when subclinic), complicatio
ns, suspicion of malignancy and/or large size (>5 cm). Adrenal gland m
ust be excised en bloc, also because of the possible presence of other
adrenal lesions. (C) 1998, Editrice Kurtis.