Current status and controversies in adrenal incidentalomas

被引:17
作者
Kaltsas, Gregory [1 ]
Chrisoulidou, Alexandra [2 ]
Piaditis, Georgios [3 ]
Kassi, Eva [4 ]
Chrousos, George [5 ]
机构
[1] Natl Tech Univ Athens, Dept Pathophysiol, Athens 11527, Greece
[2] Theagenio Hosp, Unit Endocrinol & Endocrine Oncol, Thessaloniki 54007, Greece
[3] George Genimatas Hosp, Dept Endocrinol Diabet, Athens 11527, Greece
[4] Natl Tech Univ Athens, Dept Biochem, Athens 11527, Greece
[5] Natl Tech Univ Athens, Dept Pediat 1, Athens 11527, Greece
关键词
SUBCLINICAL CUSHINGS-SYNDROME; TERM-FOLLOW-UP; PRIMARY ALDOSTERONISM; DIAGNOSTIC-ACCURACY; AUTONOMOUS CORTISOL; HIGH PREVALENCE; RISK-FACTORS; HYPERCORTISOLISM; ASSOCIATION; MANAGEMENT;
D O I
10.1016/j.tem.2012.09.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Adrenal incidentalomas (AI) are serendipitously discovered lesions during abdominal imaging studies that need to be investigated for evidence of hormonal hypersecretion and/or malignancy. Because imaging modalities can reliably identify lesions that carry a high risk of malignancy, we focus on the identification of hypersecretory lesions and those with subclinical activity, particularly Cushing syndrome. Because diverse diagnostic tests and cut-offs are employed, the prevalence of hypersecretory AI varies widely, and there is controversy regarding their long-term sequelae. In this article we provide information regarding current radiological means to define the nature of AI, and the most appropriate biochemical tests for delineating hypersecretory states. We also discuss the duration and intensity of AI follow-up as well as the identification of AI that require specific therapeutic intervention.
引用
收藏
页码:602 / 609
页数:8
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