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Updated: Dec 20, 2025

A Novel Method: Super-selective Adrenal Venous Sampling
Published on: September 15, 2017
Management of adrenal incidentalomas: Working through uncertainty
Sophie Cambos1, Antoine Tabarin2
1Department of Endocrinology, Diabetes and Nutrition, University Hospital of Bordeaux, 33604 Pessac, France.
Abstract:
The European society of endocrinology, in association with the European network for the study of adrenal tumors, published recommendations for the diagnosis and treatment of adrenal incidentalomas in 2016. A thorough and critical analysis of the literature was performed to establish evidence-based recommendations and expert suggestions with the aim of avoiding 'over-diagnosis' and 'over-treatment' and to reduce unnecessary investigations, surgery and follow-up. The purpose of this review is to reconsider several recommendations that are open to debate, such as imaging of adrenal incidentalomas, diagnosis of pheochromocytoma, diagnosis and treatment of autonomous cortisol-secreting tumors, investigations of bilateral AI and follow-up of non-operated AIs, based on studies published after the release of the recommendations.
Insights
This review critically examines 2016 European guidelines for adrenal incidentalomas, focusing on controversial areas like imaging and diagnosis of specific adrenal conditions. It aims to refine management strategies based on recent research to prevent over-treatment.
Area of Science:
- Endocrinology
- Oncology
- Radiology
Background:
- The 2016 European Society of Endocrinology guidelines addressed adrenal incidentalomas to prevent over-diagnosis and over-treatment.
- These guidelines aimed to reduce unnecessary investigations, surgery, and follow-up for adrenal incidentalomas.
Purpose of the Study:
- To critically re-evaluate specific recommendations from the 2016 guidelines.
- To incorporate recent literature published after 2016 into the assessment of adrenal incidentaloma management.
- To address debated aspects including imaging, pheochromocytoma diagnosis, autonomous cortisol secretion, and follow-up strategies.
Main Methods:
- Comprehensive literature review of studies published after the 2016 recommendations.
- Critical analysis of evidence regarding imaging, biochemical testing, and surgical indications for adrenal incidentalomas.
- Evaluation of diagnostic criteria and management protocols for specific adrenal tumor types.
Main Results:
- Identified areas of debate in the 2016 guidelines requiring updated recommendations.
- Highlighted recent studies that challenge or support existing diagnostic and treatment algorithms.
- Provided an updated perspective on the management of adrenal incidentalomas, particularly concerning autonomous cortisol secretion and pheochromocytoma.
Conclusions:
- The 2016 guidelines require reconsideration in several areas based on evolving research.
- Updated evidence supports refining diagnostic and treatment strategies for adrenal incidentalomas.
- A balanced approach is needed to avoid both under- and over-management of these tumors.
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