Adrenal incidentaloma: a diagnostic challenge

被引:53
作者
Anagnostis, Panagiotis [2 ]
Karagiannis, Asterios [2 ]
Tziomalos, Konstantinos [1 ]
Kakafika, Anna I. [2 ]
Athyros, Vasilios G. [2 ]
Mikhailidis, Dimitri P. [1 ]
机构
[1] UCL, Dept Clin Biochem, Vasc Prevent Clin, London NW3 2QG, England
[2] Aristotle Univ Thessaloniki, Hippokrat Hosp, Sch Med, Propedeut Dept Internal Med 2, GR-54006 Thessaloniki, Greece
来源
HORMONES-INTERNATIONAL JOURNAL OF ENDOCRINOLOGY AND METABOLISM | 2009年 / 8卷 / 03期
关键词
Adrenal mass; Aldosteronoma; Cushing's syndrome; Incidentaloma; Pheochromocytoma; FINE-NEEDLE-ASPIRATION; SUBCLINICAL CUSHINGS-SYNDROME; POSITRON-EMISSION-TOMOGRAPHY; DEXAMETHASONE-SUPPRESSION TEST; CLINICAL-PRACTICE GUIDELINE; MIDNIGHT SALIVARY CORTISOL; TERM-FOLLOW-UP; OF-THE-ART; PRIMARY ALDOSTERONISM; ADRENOCORTICAL CARCINOMA;
D O I
10.14310/horm.2002.1233
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
The widespread application of abdominal imaging procedures has resulted in an increased frequency of clinically silent adrenal masses. Adrenal incidentaloma (AI) is a term applied to an accidentally discovered adrenal mass on imaging performed for the investigation of an unrelated complaint. Adrenal incidentalomas (AIs) are a cluster of different pathologies, the majority of which are benign and non-functioning adrenal adenomas. However, mild hormonal alterations as well as metabolic abnormalities may be present in patients with AIs. Thus, a multidisciplinary approach with biochemical and radiologic evaluation is needed to characterize these lesions and identify patients who are at high risk for hormonal or malignant evolution. Significant new information has helped resolve controversies regarding the most reliable approach to this clinical problem. The present review considers the prevalence, pathology and natural history of AIs. We also discuss the reliability of available screening methods and localization techniques and consider optimal management and follow-up strategies.
引用
收藏
页码:163 / 184
页数:22
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