Treating pituitary tumors

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Last update26th Jan 2021

Once you have identified that a patient has a pituitary tumor, it’s important to know how to manage the patient’s treatment. Treatment approaches differ depending on whether the tumor is secreting hormones or not, and which hormones are affected.

How to treat small non-secreting pituitary tumors

Patients with small, non-secreting tumors can be monitored without treatment. These tumors will often remain unchanged in size over several decades, and patients will typically remain asymptomatic.

With the advent of modern imaging, patients with non-secreting pituitary tumors can be easily followed, and minimal increases in size will be caught. To follow a newly discovered, small, non-secreting tumor, repeat magnetic resonance imaging (MRI) after 6 months and then annually, watching for tumor growth.

If the tumor does enlarge, consult neurosurgery. The only time that a small non-secreting pituitary tumor needs to be addressed surgically is if it has shown definitive growth.

Figure 1. The magnetic resonance imaging (MRI) follow up schedule for small, non-secreting pituitary tumors involves a follow up in 6 months and then yearly afterward if no growth is seen.

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How to treat prolactin-secreting pituitary tumors

Prolactin-secreting tumors (even large ones) are initially treated with dopamine agonists such as bromocriptine or cabergoline. Generally, these medications will effectively lower prolactin levels and halt tumor growth.

Figure 2. Prolactin-secreting pituitary tumors are treated with dopamine agonists.

During treatment of a prolactin-secreting pituitary tumor, monitor prolactin levels every 3–4 months for treatment response. Usually, the initial response will involve a dramatic drop in serum prolactin within a few days. An increase in prolactin at any time may indicate tumor progression.

Figure 3. During treatment of a prolactin-secreting pituitary tumor, prolactin levels should be monitored every 3–4 months.

Prolactin-secreting tumors sometimes respond so well to dopamine agonists that they actually begin to shrink and can completely involute! If prolactin values come down to normal, continue treatment for 2–4 years and then consider gradually discontinuing the medication.

Figure 4. Dopamine agonists should be continued for 2–4 years for prolactin-secreting pituitary tumors even if prolactin levels return to normal during the treatment.

After dopamine agonists are discontinued, obtain prolactin levels every 3–4 months, and repeat the MRI at 6 and 18 months. If there is no further tumor growth at this point, and prolactin levels remain normal, the follow-up appointments can be lengthened to every two years. Sometimes (but not always) this medical regimen seems to be curative.

Figure 5. Prolactin levels should be monitored every 3–4 months, and magnetic resonance imaging (MRI) repeated at 6 and 18 months after dopamine agonist treatment is discontinued for a prolactin-secreting pituitary tumor.

Surgery should be performed for prolactin-secreting tumors if the medication fails to respond or is poorly tolerated. Some patients have significant side effects with dopamine agonists such as dizziness, headaches, nausea, vomiting, and other gastrointestinal complaints.

How to treat large non-secreting and all other hormone-secreting pituitary tumors


For large non-secreting tumors (particularly those compressing the optic apparatus), and for all other hormone-secreting tumors, surgery is the primary treatment. This is particularly true of growth hormone-, thyrotropin-, and corticotropin-secreting tumors. Large tumors can compress critical structures such as the optic chiasm, and hormone-secreting tumors can cause major metabolic and physiological derangements.

Surgery is generally performed through the nose. To best understand this approach, simply look at a midline sagittal MRI scan. There is a direct route through the nose and into the sphenoid sinus. The sella turcica, and therefore the pituitary gland, lies in the roof of the sphenoid sinus.

Figure 6. The preferred route for performing surgery on a pituitary gland tumor is the transsphenoidal route.

The surgery is generally performed using an operating microscope or endoscope. Often, otolaryngologists and neurosurgeons will perform the surgery together. This surgery is relatively safe and straightforward in the hands of an experienced neurosurgeon. Post-surgery hospitalization is generally just a few days to assure hormonal stability.

Stereotactic radiation

Stereotactic radiation has been used on some recalcitrant tumors (e.g., cannot be completely removed surgically), but it carries a risk of panhypopituitarism and optic chiasm injury. Recurrent tumors have sometimes been treated with stereotactic radiation, particularly if re-do surgery has been performed (but there is a significant residual tumor).

Figure 7. Stereotactic radiation can be used for the treatment of recalcitrant and recurrent pituitary tumors.

What to watch for after resection of a pituitary tumor

Abnormal hormone levels

After a pituitary tumor resection, ask the patient about urinary frequency and fluid ingestion. Frequent urination and increased fluid intake can be signs of diabetes insipidus caused by a deficiency in an antidiuretic hormone. These patients may urinate in tremendous volumes each day. If they are fully cognizant and can manage their oral intake well, they will compensate by drinking a lot of fluids. Nonetheless, this can result in significant electrolyte abnormalities.

Temporary diabetes insipidus is not uncommon after surgery and often resolves spontaneously. However, it can sometimes become a long-term problem. Generally, persistent diabetes insipidus should be treated with an antidiuretic hormone (ADH) analog such as desmopressin.

Consider prescribing desmopressin if the urinary frequency and the drive to drink fluids persists and reaches the nuisance level, such as causing the patient to be up multiple times at night to urinate.

Figure 8. Desmopressin can be used to treat urinary frequency after a pituitary tumor resection.

If not done by the neurosurgery or endocrinology teams, obtain a full battery of pituitary hormone levels 1–3 months postoperatively. Make sure to keep the patient involved with endocrinology specialists.

Although it is uncommon, be alert for signs of hypoadrenalism. Untreated hypoadrenalism can result in multisystem collapse and death. If you are unsure whether the patient is experiencing hypoadrenalism, it’s best to consult an endocrinologist.

Figure 9. Hormone levels, such as thyroid-stimulating hormone (TSH), T4 and prolactin, should be checked 1–3 months after a pituitary tumor resection.

Spinal fluid leakage

Spinal fluid leakage is not uncommon after pituitary surgery, particularly for macroadenomas. Be on the look-out for a spinal fluid leak. This appears as persistent clear discharge from the nose—particularly if the patient is leaning forward.

Figure 10. Spinal fluid leakage from the nose is not uncommon after pituitary tumor resection.

Sometimes, spinal fluid leakage can feel like a constant postnasal drip or a recurrent salty taste in the mouth. Imaging may not help to diagnose this issue. If the clear fluid can be collected, it can be tested for beta-2 transferrin, which would secure the diagnosis. If you suspect a spinal fluid leak, get the patient back to their surgeon.

When to obtain imaging after pituitary tumor resection

Order a contrast MRI 3–4 months after surgery to assess the tumor resection. MRI earlier than this is messy due to the detritus of surgery, and the findings are often inconclusive. Follow-up MRI and hormonal testing should be obtained 1 year postoperatively and every 1–2 years afterward if the patient is stable.

Figure 11. Follow-up hormone testing (including thyroid-stimulating hormone (TSH), T4, and prolactin) should be ordered 1-year post-surgery and every 1–2 years afterward. Magnetic resonance imaging (MRI) should be obtained 3–4 months after a pituitary tumor resection, 1 year, and every 1–2 years afterward.

That’s it for now. If you want to improve your understanding of key concepts in medicine, and improve your clinical skills, make sure to register for a free trial account, which will give you access to free videos and downloads. We’ll help you make the right decisions for yourself and your patients.

Recommended reading

  • American Association of Neurological Surgeons. 2020. Pituitary gland and pituitary tumors. American Association of Neurological Surgeons.
  • Laws, ER, Ezzat, S, Asa, SL, et al. 2013. Pituitary Disorders: Diagnosis and Management. 1st edition. New Jersey: Wiley-Blackwell.
  • Mulinda, JR. 2020. Pituitary macroadenomas. Medscape.

About the author

Gary R. Simonds, MD MHCDS FAANS
Gary is a professor at Virginia Tech Carilion School of Neuroscience and Virginia Tech Carilion School of Medicine.
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