What is the management plan for an adrenal mass?

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Last updated: August 22, 2025View editorial policy

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Management of Adrenal Masses

The management of adrenal masses requires a systematic approach including dedicated adrenal imaging, comprehensive hormonal evaluation, and risk stratification to determine the need for surgery or surveillance. 1, 2

Initial Evaluation

Imaging Assessment

  • Non-contrast CT is the first-line imaging modality:
    • Homogeneous lesions with Hounsfield units (HU) ≤10 are benign and require no additional imaging regardless of size 2, 3
    • Lesions with HU >10 require further evaluation with contrast-enhanced CT to assess washout characteristics
    • 60% washout at 15 minutes suggests benign lesion 2

Hormonal Evaluation

All patients with adrenal masses should undergo complete hormonal assessment:

  1. Cortisol Assessment:

    • 1mg overnight dexamethasone suppression test (DST)
    • Interpretation: <50 nmol/L excludes autonomous cortisol secretion; 51-138 nmol/L suggests possible autonomous cortisol secretion; >138 nmol/L indicates autonomous cortisol secretion 2
  2. Catecholamine Assessment:

    • Plasma free metanephrines or 24-hour urinary metanephrines
    • Particularly important for nodules with HU >10 on non-contrast CT
    • Values >2× upper limit of normal are diagnostic for pheochromocytoma 2
  3. Aldosterone Assessment:

    • Aldosterone-to-renin ratio for patients with hypertension and/or hypokalemia
    • Ratio >20 ng/dL per ng/mL/hr has >90% sensitivity/specificity for hyperaldosteronism 2

Management Decision Algorithm

Surgical Management Indications

Surgery is recommended for:

  1. Size-based criteria:

    • Adrenal masses >4 cm that are inhomogeneous or have HU >20 due to high risk of malignancy 3
  2. Hormone-producing tumors:

    • Pheochromocytoma: Adrenalectomy with preoperative alpha-blocker treatment 2
    • Aldosterone-secreting adenoma: Adrenalectomy (consider adrenal vein sampling prior to surgery) 2
    • Cortisol-secreting adenoma: Adrenalectomy, especially with clinically apparent Cushing's syndrome or progressive metabolic comorbidities 2
  3. Imaging characteristics concerning for malignancy:

    • Heterogeneous appearance
    • Irregular margins
    • Local invasion
    • Size >4 cm

Conservative Management

For non-functional, benign-appearing masses:

  • Asymptomatic, non-functioning unilateral adrenal masses with obvious benign features on imaging (HU <10, homogeneous) do not require surgery 3
  • Small myelolipomas (<4 cm) can be managed conservatively 2

Follow-up Protocol

For Non-operated Masses

  • Benign-appearing lesions (<10 HU; washout >50%), small (<3 cm), and non-functioning:

    • Repeat imaging in 6-12 months 2, 4
    • No further follow-up needed if stable and <4 cm 2
  • Indeterminate lesions:

    • Repeat evaluation for growth after 3-12 months 4
    • Consider surgery if growth >5 mm/year is observed 2
  • Mild Autonomous Cortisol Secretion (MACS):

    • Screen for potential cortisol-related comorbidities (hypertension, type 2 diabetes)
    • Ensure appropriate treatment of these comorbidities 3
    • Consider individualized surgical approach based on comorbidity severity 3

Special Considerations

Preoperative Preparation

  • For suspected pheochromocytoma: Preoperative alpha-blockade is essential to prevent dangerous intraoperative hypertensive crisis 2
  • For cortisol-producing tumors: Perioperative steroid coverage is required 2

Multidisciplinary Approach

  • Management requires collaboration between radiologists, endocrinologists, surgeons, and anesthesiologists 2
  • Multidisciplinary review is recommended when:
    • Imaging is not consistent with a benign lesion
    • There is evidence of hormone hypersecretion 2

Common Pitfalls to Avoid

  1. Skipping hormonal evaluation based on benign imaging appearance - Even classic-appearing myelolipomas can be hormonally active 2

  2. Overlooking subclinical hormone production - Mild autonomous cortisol secretion can contribute to metabolic comorbidities without overt Cushing's syndrome 2

  3. Inadequate preoperative preparation - Undiagnosed pheochromocytoma can lead to dangerous intraoperative hypertensive crisis 2

  4. Unnecessary surgery for small, benign, non-functioning lesions with clear benign characteristics on imaging 3

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Adrenal Myelolipoma Evaluation and Management

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Approach to the patient with an adrenal incidentaloma.

The Journal of clinical endocrinology and metabolism, 2010

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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