Adrenal incidentalomas: report of 126 cases.
- Author:
Han-zhong LI
1
;
Wei-gang YAN
;
Wei WANG
;
Ming XIA
;
Hui-jun WANG
;
Guang-hua LIU
Author Information
- Publication Type:Journal Article
- MeSH: Adolescent; Adrenal Gland Neoplasms; classification; diagnosis; therapy; Adrenocortical Adenoma; diagnosis; therapy; Adult; Aged; Child; Female; Humans; Hyperaldosteronism; diagnosis; therapy; Male; Middle Aged; Pheochromocytoma; diagnosis; therapy
- From: Chinese Journal of Surgery 2004;42(2):97-99
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo evaluate the diagnosis and treatment of adrenal incidentalomas.
METHODSOne hundred and twenty-six patients were analyzed, in which 98 patients underwent operation.
RESULTSOf all types of the adrenal incidentalomas, 52 (41.3%) of them were adenomas and they were the most often; 43 (34.1%) of them were hypersecretory adrenal tumors, most of them were pheochromocytomas and Conn adenomas; all nonhypersecretory adrenal adenomas were under 6 cm, and all adrenal carcinomas were above 6 cm.
CONCLUSIONSIt is important to search for hypersecretory adrenal tumors and to detect malignant adrenal tumors. To nonhypersecretory adrenal adenomas, the sizes of tumors are the most important indexes in determining weather the tumors are benign or malignant and weather the tumors need to be treated with operation or not.