Adrenal Disorders: Incidentalomas
With improvements in the resolution and availability of abdominal scanning (i.e., CT, MRI, and USG), many small tumors are being found in the adrenal glands incidentally—i.e. when the scan is performed during the work-up for another reason. Up to 5% of patients undergoing an abdominal CT scan will have a small adrenal mass.
(of all Incidentalomas)
55% are nonfunctioning, benign adenomas
20% are a metastasis from another primary cancer, such as breast, lung, kidney, melanoma, or lymphoma
5% are a primary adrenal cancer
20% are a hormone producing tumor—i.e., a cortisol producing tumor, an aldosteronoma (CONN SYNDROME), or a pheochromocytoma
A tumor with a mass of 5 cm or larger has a greater likelihood of being malignant.
DiagnosisThe work up of an incidental mass discovered through abdominal imaging begins by evaluating the patient for signs and symptoms of hormone overproduction. The treatment for incidentalomas depends on 2 major factors: 1) whether or not the tumor is making excess hormone and 2) the chance of the tumor being cancer. These two factors are determined by obtaining the screening blood and urine tests previously outlined, as well as a CT or MRI scan. It is vitally important to exclude the possibility of pheochromocytoma prior to operating (on any part of the body for any indication), since surgery on unprepared patients with pheochromocytoma can be fatal.
TreatmentFunctioning adrenal tumors should be surgically removed to eliminate the source of the excess hormone production. Patients with a nonfunctioning adrenal mass that is less than 3 cm should be followed by abdominal imaging every six months. The likelihood of an adrenal tumor being a cancer is heavily dependent on the tumor size. Once a tumor has reached 5 cm, the risk of developing cancer outweighs the risks of surgical removal. Tumors that are 5 cm or greater, or that are rapidly growing should, therefore, be surgically removed. Typically the surgery can be performed laparoscopically, through several very small incisions. Tumors that are between 3 cm and 5 cm may be either removed or observed depending on the patient's overall health and preferences.
CONN syndrome with adrenal incidentaloma in 51y Doctor's wife missed by Rochester Mayo clinic after five days OUT-PATIENT investigation. Also diagnosis delayed for another eight years OUT-PATIENT investigation by Toronto Teaching Hospitals internists even though BP rising, Potassium supplements needed together with severe Nocturnal polyuria. Pseudo-Diagnoses of "Chronic Fatigue Syndrome" & "Fibromyalgia" until trial of Spironolactone. BP fell immediately. Adrenal venous sampling followed soon after by L.Adrenalectomy. BP now normal without meds. No nocturnal polyuria. Rochester Mayo and Toronto University Network now actively looking for Conn syndrome.
ReplyDeleteOld style admission for investigation would have provided quick & accurate diagnosis Japanese live longest with highest hospital bed ratio.