Adrenal incidentaloma: Does an adequate workup rule out surprises?

被引:25
作者
Grogan, Raymon H. [1 ]
Mitmaker, Elliot [1 ]
Vriens, Menno R. [1 ]
Harari, Avital [1 ]
Gosnell, Jessica E. [1 ]
Shen, Wen T. [1 ]
Clark, Orlo H. [1 ]
Duh, Quan-Yang [1 ]
机构
[1] Univ Calif San Francisco, Dept Endocrine Surg, San Francisco, CA 94143 USA
关键词
ADRENOCORTICAL CARCINOMA; PHEOCHROMOCYTOMA; DIAGNOSIS;
D O I
10.1016/j.surg.2010.05.001
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background. Adrenal incidentaloma remains a diagnostic challenge. Despite well-established management guidelines, the long-term results of following these guidelines are unknown We sought to determine how accurately these guidelines identify functioning incidentalomas and how glen these guidelines result in adrenalectomy for benign tumors Methods. We catalogued adrenal incidentalomas from a retrospective review of 500 consecutive adrenlaectomies at a single institution The outcome measures studied were patient demographics, preoperative biochemical analysis, imaging characteristics, tumor size, type of operation performed, and postoperative histologic diagnosis. Results. Eighty-one of the 500 adrenaletomies performed were for incidentalomas. Size was the only significant characteristic that distinguished cortical cancers from benign adenomas. Only 1 out of 26 functioning tumors was incorrectly identified on preoperative workup We also found that 25% of cortisol-secreting incidentalomas were cystic, and that benign adenomas accounted for 42% of all tumors resected Conclusion. Current guidelines accurately predict the functional status of adrenal incidentalomas Some cystic lesions may be functioning and should therefore be screened for hormonal hypersecretion. However; even with the most up-to-date diagnostic tools available, most adrenal incidentalomas resected are benign tumors. (Surgery 2070,148:392-7.)
引用
收藏
页码:392 / 397
页数:6
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