Adrenal Incidentaloma

Author:

Sherlock Mark12ORCID,Scarsbrook Andrew3,Abbas Afroze4ORCID,Fraser Sheila5,Limumpornpetch Padiporn6,Dineen Rosemary12ORCID,Stewart Paul M6ORCID

Affiliation:

1. Department of Endocrinology, Beaumont Hospital, Dublin, Ireland

2. Royal College of Surgeons in Ireland, Dublin, Ireland

3. Department of Radiology, Leeds Teaching Hospitals NHS Trust, St James University Hospital, Leeds, UK

4. Department of Endocrinology, Leeds Teaching Hospitals NHS Trust, St James University Hospital, Leeds, UK

5. Department of Endocrine Surgery, Leeds Teaching Hospitals NHS Trust, St James University Hospital, Leeds, UK

6. Faculty of Medicine & Health, University of Leeds, Worsley Building, Clarendon Way, Leeds, UK

Abstract

Abstract An adrenal incidentaloma is now established as a common endocrine diagnosis that requires a multidisciplinary approach for effective management. The majority of patients can be reassured and discharged, but a personalized approach based upon image analysis, endocrine workup, and clinical symptoms and signs are required in every case. Adrenocortical carcinoma remains a real concern but is restricted to <2% of all cases. Functional adrenal incidentaloma lesions are commoner (but still probably <10% of total) and the greatest challenge remains the diagnosis and optimum management of autonomous cortisol secretion. Modern-day surgery has improved outcomes and novel radiological and urinary biomarkers will improve early detection and patient stratification in future years to come.

Publisher

The Endocrine Society

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

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