- A functioning adrenal tumor (secreting aldosterone, catecholamines, or cortisol)
- If an adrenal mass is suspected to harbor cancer:
- Attenuation and washout not consistent with benign lesions
- Size >4 cm, and enlarging with time
- Atypical imaging, irregular borders, enhancement of mass, heterogeneity, calcification, and necrosis
- Plasma-free metanephrines, which harbor a sensitivity of 97-100%, and a specificity of 85-89%.
- 24-hour urinary metanephrines
- Adequate hydration and salt intake
- Preoperative blockade with alpha-adrenergic blockade (for several weeks before surgery until the patient’s blood pressure has normalized). For this purpose, either phenoxybenzamine or doxazosin can be used.
- Administration of a beta blocker, which must be given after alpha blockade. For this purpose, either metoprolol, propranolol, or atenolol can be used.
- Alpha methyltyrosine (metyrosine), which is a tyrosine kinase inhibitor, can be given to the patients in an attempt to inhibit catecholamine production
Dr. Rogers concluded his talk and discussed the rare procedure of partial adrenalectomy. Its indications include:
- Bilateral disease
- Solitary adrenal gland
- Familial syndromes (VHL, MEN2, SDH, NF1)
During partial adrenalectomy, it is important to mobilize the adrenal limb with the tumor and use intraoperative ultrasound to delineate the exact location of the tumor. Clips should be used along the resection line to reduce bleeding, and it is preferable to avoid excessive thermal injury to the spared adrenal limb.
Presented by: Craig Rogers, MD, Henry Ford Health System, Detroit, Michigan
Written By: Hanan Goldberg, MD, Urologic Oncology Fellow (SUO), University of Toronto, Princess Margaret Cancer Centre @GoldbergHanan at 2019 3rd Annual North American Robotic Urology Symposium (NARUS), February 8-9, 2018 - Las Vegas, Nevada, United States