Pituitary Tumors

The pituitary gland
The pituitary gland produces critical hormones, so even a benign tumor may interfere with or impair the gland’s function.

What Doctors Treat Pituitary Tumors?
A pituitary tumor is most commonly adenoma, which is a tumor that arises from the cells of the pituitary gland. Although it is usually benign (not cancerous), a pituitary tumor is not harmless. Since the pituitary gland produces critical hormones, a tumor may interfere with or destroy the gland’s function. Some pituitary tumors are “functioning” tumors, meaning the tumor itself produces hormones. The good news is that advanced new methods for diagnosing and removing pituitary tumors have made it possible for expert neurosurgeons to treat these lesions using minimally invasive techniques that leave little or no scarring (see Surgery for Pituitary Tumors).

When a pituitary tumor is said to be “functioning,” that means it’s producing one or more hormones: prolactin, adrenocorticotrophic hormone, growth hormone, or thyrotropin. Since these hormones play different roles in the body, the symptoms of a pituitary tumor can be very different depending on which hormone the tumor is producing.

The pituitary gland is located at the base of the skull, not technically within the brain itself. There are other tumors that may appear at the skull base near the pituitary gland, in an area called the sellar/parasellar region, but that are not technically pituitary tumors. These other tumors include:

In less common cases, a pituitary tumor may be an invasive adenoma or a carcinoma. Minimally invasive surgical techniques may be used to remove any of these tumors.

What Causes a Pituitary Tumor?
Researchers don’t know for sure what causes a pituitary tumor to develop. Some people seem to have a genetic predisposition to them — if a parent or grandparent had a pituitary tumor you may be at greater risk — but many tumors are “sporadic,” meaning they simply develop for no known reason. Very rarely a pituitary adenoma can be part of a genetic/familial syndrome such as multiple endocrine neoplasia, type I (MEN1). Since pituitary tumors do not always cause symptoms, you can have one and not know it — in fact they are fairly common and may be present in up to 10 percent of the population.

At Weill Cornell Medicine Neurological Surgery, our neurosurgeons are highly skilled in the most advanced procedures for treating brain tumors. Our relationship with NewYork/Presbyterian Hospital allows our surgeons access to the very best facilities and specialists, as well as the most leading-edge research laboratories, to ensure that you get the very best treatment available. We use specialized imaging sequences to identify the tumors and, in some circumstances, we use a new procedure called inferior petrosal sinus sampling to identify and localize ACTH-producing tumors.

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Our Care Team

  • Chief of Neurological Surgery, NewYork-Presbyterian Brooklyn Methodist
  • Professor, Neurological Surgery
  • Director, Brain Metastases Program
  • Co-director, William Rhodes and Louise Tilzer-Rhodes Center for Glioblastoma
Phone: 212-746-1996 (Manhattan) / 718-780-3070 (Brooklyn)
  • Associate Professor of Neuroendocrinology in Neurological Surgery, Weill Cornell Medicine
Phone: 646-962-3556
  • Associate Professor, Neurological Surgery
Phone: 718-670-1837
  • Professor of Clinical Neurological Surgery
Phone: 212-746-2438
  • Chief of Neurological Surgery, NewYork-Presbyterian Queens
  • Professor of Clinical Neurological Surgery
  • Co-director, Weill Cornell Medicine CSF Leak Program
Phone: (718) 670-1837
  • Associate Professor of Clinical Neurological Surgery
Phone: 718-780-5176
  • Endocrinologist
Phone: (646) 962-8690
  • Endocrinologist
Phone: (646) 962-8690

Reviewed by: Georgiana Dobri, M.D.
Last reviewed/last updated: September 2023
Illustration by Thom Graves, CMI

Weill Cornell Medicine Neurological Surgery 525 East 68 Street, Box 99 New York, NY 10065 Phone: 866-426-7787