What is the management plan for a patient with a suspected adrenal adenoma, elevated cortisol levels, and symptoms of agitation?

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Management of Adrenal Adenoma with Elevated Cortisol and Agitation

For a patient with suspected adrenal adenoma, elevated cortisol levels, and agitation, surgical removal of the adenoma through adrenalectomy is the recommended management approach, especially given the presence of symptomatic cortisol excess. 1

Diagnostic Evaluation

Initial Imaging Assessment

  • Non-contrast CT is the first-line imaging modality for adrenal masses
    • Lesions with Hounsfield units (HU) ≤10 are likely benign adenomas
    • Lesions >4 cm, with HU >20, or inhomogeneous appearance suggest higher malignancy risk 1
  • For indeterminate lesions:
    • Contrast-enhanced CT washout studies (>60% washout at 15 minutes suggests benign lesion)
    • Chemical shift MRI (signal intensity loss in opposed-phase images indicates benign adenoma) 1

Hormonal Evaluation

A complete hormonal assessment is essential for all adrenal masses, regardless of imaging appearance:

  1. Cortisol Assessment:

    • 1mg overnight dexamethasone suppression test (DST)
    • Serum cortisol ≥1.8 μg/dL after DST suggests cortisol excess 1, 2
    • Assess diurnal rhythm of cortisol secretion (elevated late-night cortisol suggests Cushing's syndrome) 3
  2. Catecholamine Assessment:

    • Plasma-free or 24-hour urinary fractionated metanephrines
    • Critical to rule out pheochromocytoma before any invasive procedure 1
  3. Aldosterone Assessment:

    • Aldosterone-to-renin ratio to screen for primary aldosteronism 1

Management Algorithm for Adrenal Adenoma with Hypercortisolism

For Cortisol-Secreting Adenoma with Symptoms (as in this case):

  1. Surgical Management:

    • Adrenalectomy is the treatment of choice for cortisol-secreting adenomas causing clinical symptoms 1
    • Perioperative steroid coverage is mandatory to prevent adrenal crisis 1
    • Laparoscopic approach is preferred when technically feasible
  2. Preoperative Considerations:

    • Management of comorbid conditions (hypertension, diabetes, etc.)
    • Prophylactic antibiotics
    • Adequate steroid coverage to prevent adrenal insufficiency 4
  3. Postoperative Management:

    • Monitor for temporary adrenal insufficiency, which occurs in approximately 50% of patients after removal of cortisol-producing adenomas 5
    • Gradual tapering of glucocorticoid replacement therapy
    • Follow-up cortisol testing to assess recovery of HPA axis function

For Subclinical Cushing's Syndrome (if symptoms were less pronounced):

  • Shared decision-making between surgery vs. conservative management based on:
    • Patient preference
    • Severity of comorbidities
    • Risk of progression 4
  • Consider surgery if there are metabolic complications (hypertension, diabetes, obesity) 5

Management of Associated Symptoms

For Agitation and Neuropsychiatric Symptoms:

  • Recognize that cortisol excess commonly causes mood changes, anxiety, and agitation 1
  • Address these symptoms through:
    • Treating the underlying cause (adrenalectomy)
    • Temporary symptomatic management while awaiting surgery
    • Monitor for improvement after normalization of cortisol levels

Important Clinical Considerations

Pitfalls to Avoid:

  1. Do not delay diagnosis - subclinical Cushing's syndrome is the most common hormonal dysfunction caused by adrenal incidentalomas 4
  2. Do not skip hormonal evaluation based on benign imaging appearance, as even radiologically benign-appearing lesions can be hormonally active 1
  3. Do not perform biopsy of suspected adrenal masses, as biopsies are usually not informative and may trigger complications 1
  4. Do not forget perioperative steroid coverage for patients undergoing surgery for cortisol-producing adenomas 4

Expected Outcomes:

After surgical removal of cortisol-producing adenomas, patients typically experience:

  • Improvement in hypertension
  • Weight loss in obese patients
  • Better metabolic control of diabetes
  • Resolution of neuropsychiatric symptoms including agitation 5

Long-term follow-up is mandatory to ensure complete resolution of hypercortisolism and associated symptoms 3.

References

Guideline

Adrenal Nodule Evaluation

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Cushing's syndrome.

Journal of surgical oncology, 2012

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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