- Clinically or biochemically apparent adrenal hormonal hyperfunction.
- Possible or certain malignant adrenal mass.
- Adrenal mass of uncertain significance.
- Primary hyperaldosteronism.
- Unilateral cortical adenoma causing Conn’s syndrome.
- Bilateral hyperplasia with unilateral dominance (established by adrenal vein sampling).
- Unilateral cortical adenoma causing Conn’s syndrome.
- Hypercortisolism.
- Unilateral cortical adenoma.
- Refractory Cushing’s syndrome (from Cushing’s disease, primary adrenal hyperplasia, or ectopic adrenocorticotropic hormone [ACTH] syndrome).
- Unilateral cortical adenoma.
- Pheochromocytoma.
- Unilateral cortical adenoma causing virilization.
- Myelolipoma (in selected situations).
- Adrenal cyst (if refractory or symptomatic).
- Adrenocortical carcinoma.
- Incidentaloma with indeterminate or concerning imaging characteristics.
- Adrenal metastases of other primary cancers (in selected situations).
- Adrenocortical carcinoma (certain or likely).
- Refractory coagulopathy.
- Comorbidities precluding safe general anesthesia.
- Previous ipsilateral partial adrenal resection.
- Previous extensive upper abdominal or retroperitoneal surgery.
- Very large adrenal tumors (> 6–8 cm).
- Suboptimal medical preparation for pheochromocytoma resection.