
What is the pituitary stalk?
The pituitary stalk (also known as the infundibular stalk, Fenderson's funnel, or simply the infundibulum) is the connection between the hypothalamus and the posterior pituitary.
How does the pituitary gland communicate with the hypothalamus?
Your pituitary gland is connected to your hypothalamus through a stalk of blood vessels and nerves (the pituitary stalk). Through that stalk, your hypothalamus communicates with the anterior pituitary lobe via hormones and the posterior lobe through nerve impulses.
What does the pituitary gland do?
It sits in its own little chamber under your brain known as the sella turcica. It’s a part of your endocrine system and is in charge of making several essential hormones. Your pituitary gland also tells other endocrine system glands to release hormones.
What is pituitary stalk interruption syndrome?
Pituitary Stalk Interruption Syndrome PSIS is a congenital defect of the pituitary gland characterized by a thin or interrupted pituitary stalk, anterior pituitary hypoplasia, and an ectopic posterior pituitary. Patients may present with an isolated pituitary hormone deficiency or with combined hypothalamic-pituitary hormone deficiencies.

What happens if pituitary stalk is cut?
The pituitary stalk is the thin vertical blue portion. This connection is called the hypothalamo-hypophyseal tract or hypothalamo-neurohypophyseal tract. Damage to the pituitary stalk blocks the release of antidiuretic hormone, resulting in polydipsia (abusive water intake) and polyuria (excessive urination).
What is the pituitary gland stalk?
The pituitary stalk, known as the infundibulum or infundibular stalk, is the connection between the hypothalamus and the pituitary gland, especially the posterior pituitary gland.
Does the pituitary stalk produce hormones?
The pituitary gland is located inferior to the hypothalamus and is connected to the hypothalamus by a stalk. Hormonal secretion by the anterior pituitary is controlled by hypothalamic-releasing hormones that reach their target endocrine tissues in the anterior pituitary via the pituitary stalk.
What causes a deviated pituitary stalk?
Patients with leukemia and pituitary stalk thickening, clinically, also have DI [1 ]. In conclusion, pituitary stalk lesions have diverse causes. The abnormalities of the pituitary stalk fall into three main categories: congenital lesions, inflammatory/ infectious lesions, and neoplasms.
Is the pituitary stalk part of the brain?
The pituitary stalk acts as a physical connection between the pituitary gland and brain and contains the hypophyseal (hypothalamic-pituitary) portal system as well as the neuronal connections traversing across the hypothalamic median eminence.
Can you live without your pituitary gland?
You can live without your pituitary gland as long as you take medication to replace the pituitary hormones that you're missing. The pituitary gland hormones are very important for maintaining several bodily functions. An untreated lack of all the pituitary hormones is life-threatening.
What is stalk effect?
Abstract. Most patients with large pituitary tumors do not exhibit hyperprolactinemia as a result of pituitary lactotroph disinhibition (stalk effect). Studies have demonstrated that increased intrasellar pressure is associated with both "stalk effect" hyperprolactinemia and pituitary insufficiency.
What happens if pituitary gland is not functioning properly?
For example, if the pituitary gland does not produce enough growth hormone in a child, they may have a permanently short stature. If it doesn't produce enough follicle-stimulating hormone or luteinizing hormone, it might cause problems with sexual function, menstruation, and fertility.
What size pituitary tumor is considered large?
Large pituitary tumors — those measuring about 1 centimeter (slightly less than a half-inch) or larger — are known as macroadenomas. Smaller tumors are called microadenomas. Because of the size of macroadenomas, they can put pressure on the normal pituitary gland and nearby structures.
What are the symptoms of a tumor on your pituitary gland?
Pituitary Gland Tumor: Symptoms and SignsHeadaches.Vision problems.Unexplained tiredness.Mood changes.Irritability.Unexplained changes in menstrual cycles.Erectile dysfunction, which is the inability to achieve or maintain an erection and is caused by hormone changes.Infertility, which is the inability to have children.More items...
Is a pituitary tumor a brain tumor?
A tumor that develops in the pituitary gland is typically considered to be a type of brain cancer. The pituitary gland, which is responsible for producing and releasing hormones into the body, is located inside the skull, just beneath the brain and above the nasal passages.
What is stalk effect?
Abstract. Most patients with large pituitary tumors do not exhibit hyperprolactinemia as a result of pituitary lactotroph disinhibition (stalk effect). Studies have demonstrated that increased intrasellar pressure is associated with both "stalk effect" hyperprolactinemia and pituitary insufficiency.
What does thickening of the pituitary stalk mean?
Conclusion: Pituitary stalk width could indicate the presence of anterior pituitary dysfunction, especially in central diabetes insipidus patients. With the use of a diagnostic model, the neoplastic and inflammatory causes of pituitary stalk thickening could be preliminarily differentiated.
What is a pituitary stalk transection?
Pituitary stalk transection was described after the introduction of MRI and comprises a small anterior pituitary gland, thin or absent infundibulum after gadolinium administration, and an ectopic location of the posterior pituitary [12].
What is pituitary stalk interruption syndrome?
Pituitary stalk interruption syndrome is characterized by absence or marked thinning of the pituitary stalk, nonidentification of the normal posterior bright spot of the neurohypophysis, the presence of the bright spot in the floor of the third ventricle in the region of the median eminence or along the infundibulum (ectopic posterior pituitary), and commonly small size of the adenohypophysis (Abernethy, 1998) ( Fig. 63.25 ). Isolated growth hormone deficiency or multiple pituitary hormone deficiencies occur. Mutations of HESX1, LHX4, OTX2, and SOX3 genes have been occasionally implicated. The severity of abnormality of the stalk (absence versus thinning) correlates with the severity and multiplicity of hormone deficiencies ( Wang et al., 2014 ).
What is incomplete pituitary isolation syndrome?
An incomplete pituitary isolation syndrome may occur with the empty sella syndrome, intrasellar cysts, or pituitary adenomas. 335,336 Anterior pituitary failure after stalk section is in part due to loss of specific neural and vascular links to the hypothalamus and in part due to pituitary infarction.
What is the thickness of the pituitary stalk?
The thickness of the normal pituitary stalk is approximately 2 mm. The normal stalk enhances markedly on CT and MRI with contrast. The most common clinical problem associated with disease of the pituitary stalk is diabetes insipidus. When this is present, there usually is absence of the normal hyperintensity of the posterior pituitary noted on T1-weighted MRI. Diabetes insipidus may also occur as a result of transection of the pituitary stalk.
What causes hypertrophy in rats?
Following transection of the pituitary stalk or presence of hypothalamic lesions which destroy the supraoptic and paraventricular nuclei, the intermediate lobe of the rat and other species may show hypertrophy and hyperplasia.67 Hypertrophy and hyperplasia can also result from interference with dopaminergic-control mechanisms by administration of xenobiotics. Chronic treatment of rats with haloperidol, a dopamine receptor antagonist, stimulates the secretion of α-MSH and β endorphin and accelerates the synthesis of pro-opiomelanocortin. This is associated with an increase in the number of cell layers in the intermediate lobe. The thickened gland contains many dark melanotrophs which do not appear increased in size but contain more mRNA for pro-opiomelanocortin than controls as shown by in situ hybridization. 36 Hyperplasia of the intermediate lobe is also observed spontaneously in Syrian hamsters with advancing age. 68
What is the role of the hypothalamus in the nervous system?
This small subdivision of the ventral diencephalon communicates extensively with other regions of the neuraxis via classical synaptic interactions, and plays an essential role in coordinating behavioral and emotional state with peripheral physiology through its regulatory influences over the autonomic nervous system and pituitary gland. In essence, it is directly responsible for the regulation of homeostatic systems essential for the survival of the parent organism and perpetuation of the species . The ability of this subdivision of the diencephalon to exert such profound influences over behavioral state and physiology is reflected in both the properties of hypothalamic neurons and the mechanisms through which they communicate. This article reviews basic organizational principles fundamental to hypothalamic function, focusing upon well-studied hypothalamic systems that illustrate the functional diversity of this small but influential region of the brain. We begin with a brief historical perspective, progress to a description of basic features of hypothalamic structure and connectivity, and finish with a consideration of four regulatory systems through which hypothalamic neurons exert their influence. Throughout we emphasize the cooperative interactions among functionally diverse systems that permit precise adjustments of physiology in support of adaptive behavior.
What connects the pituitary gland to the hypothalamus?
The pituitary stalk, which connects the hypothalamus to the pituitary gland, carries both blood vessels and nerve fibres. The anterior pituitary is connected to the hypothalamus by a vascular connection through the hypophyseal portal system. A portal system is a vascular connection with two sets of capillary beds. The first set of capillaries is in the hypothalamus and blood passes through the portal veins in the pituitary stalk to the second set of capillaries in the anterior pituitary (Fig. 3.4 ). In this way, agents released from the hypothalamus can be delivered to the pituitary where they act on pituitary cells to control hormone synthesis and release.
Overview
Hypopituitarism is a rare condition in which there’s a lack (deficiency) of one, multiple or all of the hormones made by your pituitary gland. Hormones are chemicals that coordinate different functions in your body by carrying messages through your blood to your organs, muscles and other tissues.
Symptoms and Causes
The symptoms of hypopituitarism depend on which pituitary hormone (s) are affected and deficient (lacking). The following factors also affect what kind of symptoms you’ll experience:
Diagnosis and Tests
Your healthcare provider may order any of the following tests to diagnose hypopituitarism:
Management and Treatment
Treatment for hypopituitarism depends on which pituitary hormone (s) are deficient and the cause of the hypopituitarism. For that reason, treatment is very individualized. Your healthcare team will determine what the best treatment plan is for you. Common treatment options for hypopituitarism include:
Prevention
The following conditions or situations are considered risk factors for hypopituitarism:
Living With
In most cases, hypopituitarism requires close, lifelong monitoring of the hormones affected. Be sure to see your healthcare provider regularly to make sure your treatment plan is working. If you’re experiencing new or concerning symptoms, contact your healthcare provider as soon as possible.
What is the Pacific Pituitary Disorders Center?
At the Pacific Pituitary Disorders Center we have one of the world’s largest and most extensive experiences in diagnosing and treating patients with hypopituitarism of all causes. Our team of pituitary endocrinologists and neurosurgeons work closely together to preserve or restore pituitary gland function and quality of life.
How to treat hypophysitis?
Treatment of hypophysitis is typically with hormone replacement therapy and with high dose glucocorticoids (steroids) to reduce inflammation. Despite long-term treatment with steroids, most patients do develop some degree of permanent pituitary gland failure.
Can a pituitary biopsy confirm hypophysitis?
In a minority of patients with presumed hypophysitis, a pituitary biopsy may be warranted to confirm the diagnosis if MRI findings are not completely convincing. Pituitary surgery may also be indicated for patients with visual loss from the enlarged pituitary gland impinging upon the optic nerves or optic chiasm.
