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Treatment of symptomatic empty sella syndrome would typically involve replacement therapy for any deficient hormones.

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Treatment of symptomatic empty sella syndrome would typically involve replacement therapy for any deficient hormones.

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yes

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Primary empty sella syndrome is thought to be congenital (present at birth) in most cases, and is caused by a failure or opening of the diaphragma sella. This may be an accidental occurrence, with no known triggering or causative factors.

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You might have a pituary growth. This is called empty sella syndrome.

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Definition

Empty sella syndrome is a condition in which the pituitary gland shrinks or becomes flattened.

Causes, incidence, and risk factors

The pituitary gland is a small gland located at the base of the brain. It sits in a saddle-like compartment in the skull called the "sella turcica," which in Latin means "Turkish saddle."

When the pituitary gland shrinks or becomes flattened, it cannot be seen on MRIscans, giving the appearance of an "empty sella." This is referred to as empty sella syndrome.

The pituitary makes several hormones that control the other glands in the body, including the:

  • Adrenal glands
  • Ovaries
  • Testicles
  • Thyroid

Primary empty sella syndrome occurs when a hole in the membrane covering the pituitary gland allows fluid in, which presses on the pituitary.

Secondary empty sella syndrome occurs when the sella is empty because the pituitary gland has been damaged by:

  • A tumor
  • Radiation therapy
  • Surgery

Empty sella syndrome may be seen in a condition called pseudotumor cerebri. This is a condition seen most commonly in obese women.

Symptoms

Often, there are no symptoms or loss of pituitary function.

Patients with empty sella syndrome may have symptoms caused by a partial or complete loss of pituitary gland function. For more information, see hypopituitarism.

Symptoms include:

Signs and tests

Primary empty sella syndrome is most often discovered during radiological imaging of the brain. Pituitary function is usually normal.

The health care provider may test pituitary gland function to make sure that the gland is working normally.

Sometimes tests for high pressure in the brain will be done, such as:

  • Examination of the retina by an ophthalmologist
  • Lumbar puncture (spinal tap)

The hormone prolactin is a little high in a small percentage of patients, which may interfere with the normal function of the testicles or ovaries.

Treatment

For primary empty sella syndrome:

  • There is no specific treatment if pituitary function is normal.
  • Medications, such as bromocriptine, which lower prolactin levels, may be prescribed if the prolactin levels are high and interfering with function of the ovaries or testes.

For secondary empty sella syndrome:

  • Treatment involves replacing the hormones that are lacking.
Expectations (prognosis)

Primary empty sella syndrome does not cause health problems, and it does not affect life expectancy.

Complications

Complications of primary empty sella syndrome include mild hyperprolactinemia.

Complications of secondary empty sella syndrome are related to the cause of pituitary gland disease or to the effects of too little pituitary hormone.

Calling your health care provider

Contact your health care provider if you develop symptoms of abnormal pituitary function, such as a disrupted menstrual cycle or impotence.

References

Melmed S, Kleinberg D. Anterior pituitary. In: Kronenberg HM, Melmed S, Polonsky KS, Larsen PR, eds. Williams Textbook of Endocrinology. Philadelphia, PA: Saunders Elsevier; 2008:chap 8.

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