|
:
Endocrine Service:
Surgery Tutorials:
Adrenal Mass
Hypercalcemia
(High Calcium Levels) and Parathyroid Disease
Neck
(Thyroid) Mass
Thyroid
Cancer
Surgical Approach to the Adrenal
Surgical Approach for Hyperparathyroidism
Surgical
Approach for Thyroid Mass
|
|
The adrenal glands are two glands situated on
either side of the body above the right and left kidney. Each is
approximately 4 centimeters long and 1 centimeter in width. The adrenal
glands produce a variety of important metabolic hormones. A single adrenal
gland can be removed without significant consequence to hormone levels.
However, the patient with both adrenal glands removed will require adrenal
hormone supplementation for the remainder of his or her life.
The patient with an adrenal mass is usually diagnosed in one of two
ways. The first, and more common, is the incidental finding of an adrenal
mass found on a CT scan, obtained for other reasons such as trauma or
backache. The second would be the finding of an adrenal mass in the
evaluation of a patient who has a hormone excess state. This finding may
be indicative of a mass that is over secreting one of its important
hormones.
The evaluation of the patient with an adrenal mass in either category
includes the referral to an endocrine surgeon by their primary care
physician or a referring specialist endocrinologist. The workup will
include a careful family history, in order to evaluate for a familial
endocrine pattern of such masses. Further workup will involve blood work
and usually one or two 24-hour urine collections for hormones.
Functioning adrenal tumors are usually one of four varieties:
- Aldosterone Secreting Tumors:
These are usually unilateral tumors
of the adrenal cortex, which secrete a hormone called aldosterone.
Elevated aldosterone levels result in low potassium levels and high
blood pressure levels. These patients have a significant history of high
blood pressure and require potassium supplementation.
- Pheochromocytoma:
These can occur in families (MEN II syndrome)
or be non-familial or sporadic. Such patients classically have a history
of flushing or hypertension. These patients will have their diagnosis
confirmed by 24-hour urinary levels looking for a hypertensive hormone
secreted by the tumor. Familial screening and evaluation for pituitary,
thyroid, and parathyroid dysfunction may be recommended.
- Cushing's syndrome:
In this circumstance, an unexplained stimulus
causes the adrenal glands to secrete too much cortisol or steroids. This
can result in a patient with obesity and hypertension, muscle weakness
and edema. The stimulus may occur from within the adrenal gland itself.
The diagnosis is usually made from the analysis of 24-hour urine for
cortisol levels. If a single lesion causes the abnormality in one of the
adrenal glands then surgical removal is recommended. It may also occur
as a result of a mass or dysfunction elsewhere within the body such as
the pituitary gland (near the brain). If treatment of the pituitary
gland abnormality is not successful, removal of the adrenal glands may
be required.
- Adreno-genital syndrome:
The patients with this type of adrenal
dysfunction are usually children who present with sex hormone
abnormalities and inappropriate genital growth. A pediatric
endocrinologist will evaluate these patients through CT and urine
collections.
- Non-functioning adrenal masses:
The patient with the incidentally
discovered adrenal mass must be carefully evaluated looking at the
family history, personal history, evaluation of the image and by
chemical evaluation is mentioned above. In an asymptomatic mass the
physician must consider the possibility of a very rare form of primary
cancer within the adrenal gland. Adrenal cancer is very deadly and
rapidly progressive. Most patients with an adrenal mass of less than 3
centimeters have very little to worry about concerning the diagnosis of
cancer. These patients should have a follow-up CT scan within six months
and, if any growth or symptoms develop, consider resection. If a
follow-up six-month CT scan confirms that this is a stable lesion, it
may be safely followed without surgery. In most cases this growth has
probably been there many years prior to its discovery (adrenal adenoma).
The prevailing opinion about non-functional adrenal masses over 4 to
5 centimeters is that they should be removed. It is generally noted that
the incidence of cancer is increased in adrenal masses over 4
centimeters in size.
|