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Differences Between Bilateral Adrenal Incidentalomas and Unilateral Lesions
Jesse D Pasternak1, Carolyn D Seib1, Natalie Seiser1
1Section of Endocrine Surgery, Department of Surgery, University of California, San Francisco.
Bilateral adrenal incidentalomas are more often linked to subclinical Cushing syndrome and rarely pheochromocytomas. This finding suggests a need for increased vigilance for Cushing syndrome in patients with bilateral adrenal lesions.
Area of Science:
- Endocrinology
- Oncology
- Radiology
Background:
- Adrenal incidentalomas are common findings during abdominal imaging.
- While unilateral adrenal lesions have established workups, bilateral incidentalomas are less understood.
- Limited data exists on the natural history and clinical implications of bilateral adrenal incidentalomas.
Purpose of the Study:
- To compare the natural history of patients with bilateral adrenal incidentalomas versus those with unilateral adrenal incidentalomas.
- To identify differences in prevalence of endocrine disorders between bilateral and unilateral adrenal incidentalomas.
- To inform clinical management strategies for patients with bilateral adrenal incidentalomas.
Main Methods:
- Retrospective analysis of a prospective database from a tertiary care university hospital.
- Inclusion of 500 patients with adrenal lesions evaluated between July 2009 and July 2014.
- Comparison of patient demographics, imaging characteristics, biochemical workup, interventions, and diagnoses between bilateral and unilateral incidentaloma groups.
Main Results:
- Twenty-three patients had bilateral incidentalomas, and 112 had unilateral incidentalomas.
- Bilateral incidentalomas showed a higher prevalence of subclinical Cushing syndrome (21.7% vs 6.2%) and a lower prevalence of pheochromocytoma (4.3% vs 19.6%) compared to unilateral lesions.
- Rates of hyperaldosteronism were similar between groups; no occult adrenocortical carcinomas were found.
Conclusions:
- Bilateral adrenal incidentalomas are significantly associated with subclinical Cushing syndrome and less frequently with pheochromocytoma.
- Despite similar workups, the distinct natural history of bilateral incidentalomas necessitates a higher index of suspicion for subclinical Cushing syndrome.
- These findings underscore the importance of tailored diagnostic approaches for bilateral adrenal incidentalomas.
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