
- Abnormal slowing of growth.
- Delayed puberty.
- Excessive thirst and excessive urination.
- Less frequent menstrual periods.
- Low blood sugar (hypoglycemia)
- Prolonged jaundice in infants.
- Sensitivity to cold.
- Poor appetite.
What are the symptoms of hypopituitarism?
They are sometimes subtle and may be overlooked for months or even years. Signs and symptoms of hypopituitarism vary, depending on which pituitary hormones are deficient and how severe the deficiency is. They may include: Fatigue. Weight loss. Decreased sex drive. Sensitivity to cold or difficulty staying warm.
What is panhypopituitarism in children?
Panhypopituitarism in Children 1 Panhypopituitarism is a condition in which the production... 2 Causes of panhypopituitarism. Pituitary hormone production is regulated by the hypothalamus... 3 Signs and symptoms of panhypopituitarism. Symptoms of panhypopituitarism vary widely,... 4 Testing and diagnosis for panhypopituitarism. Your doctor...
Should I talk to my doctor about my panhypopituitarism symptoms?
Most cases of panhypopituitarism require lifelong treatment and monitoring of your hormones, so it’s important to see your provider regularly. Be sure to contact your provider if you have new or concerning symptoms. They’re available to help. Last reviewed by a Cleveland Clinic medical professional on 08/03/2022.
What are the risks of panhypopituitarism?
If panhypopituitarism develops slowly or rapidly. How quickly you get a diagnosis and receive treatment. Panhypopituitarism is associated with significant decreases in quality of life and life expectancy. People with panhypopituitarism often develop obesity, decreased lean body mass and an increased risk of cardiovascular disease.

How is panhypopituitarism diagnosed?
Hormone tests for diagnosing panhypopituitarism Hormone level tests include: Blood tests: Pituitary gland hormones that providers can measure through simple blood tests include thyroid-stimulating hormone (TSH), prolactin, follicle-stimulating hormone (FSH) and luteinizing hormone (LH).
What is a panhypopituitarism mean?
(pan-HY-poh-pih-TOO-ih-tuh-rih-zum) A rare condition in which the pituitary gland stops making most or all hormones. Pituitary hormones help control the way many parts of the body work.
What is the difference between hypopituitarism and panhypopituitarism?
The pituitary makes hormones that are needed for normal body functions. When you do not have two or more of the pituitary hormones, it is known as hypopituitarism (hahy-poh-pi-too-i-tuh-riz-uh m). The lack of all pituitary hormones is known as panhypopituitarism.
Is panhypopituitarism life threatening?
pituitary hormones is known as panhypopituitarism, a serious and sometimes fatal disorder.
How do you treat panhypopituitarism?
TreatmentCorticosteroids. These drugs, such as hydrocortisone (Cortef) or prednisone (Rayos), replace the adrenal hormones that aren't being produced because of an adrenocorticotropic hormone (ACTH) deficiency. ... Levothyroxine (Levoxyl, Synthroid, others). ... Sex hormones. ... Growth hormone. ... Fertility hormones.
How common is panhypopituitarism?
Hypopituitarism is listed as a rare disorder by the National Institutes of Health (NIH), affecting less than 200,000 individuals in the United States.
Does panhypopituitarism shorten life expectancy?
Growing, but not completely conclusive, evidence indicates that childhood hypopituitarism may be associated with a shortened adult lifespan, even with adequate hormonal replacement.
What is the most common cause of hypopituitarism?
Pituitary adenomas: One of the most common causes of primary hypopituitarism is a pituitary adenoma (a benign, or noncancerous, tumor).
What happens if hypopituitarism is left untreated?
It is essential that the condition is diagnosed and treated as soon as possible, because untreated hypopituitarism has the potential to lead to permanent disability or death.
Who is at risk of panhypopituitarism?
Risk Factors Factors that may increase your chance of panhypopituitarism include: Damage to the pituitary gland, which may occur from trauma , radiation therapy , cancer spread, bleeding after childbirth (postpartum hemorrhage) Tumor of the pituitary gland.
Is panhypopituitarism curable?
It is treatable, and a patient with this condition should be able to perform normal activities as long as the appropriate hormonal therapy is used consistently and properly. Even after the proper regimen has been established, a patient with hypopituitarism requires lifelong medical follow-up.
How do you know if your pituitary gland is not working?
In adults, symptoms include low energy, decreased strength and exercise tolerance, weight gain, decreased muscle mass, and feelings of anxiety or depression.
Does Panhypopituitarism shorten life expectancy?
Growing, but not completely conclusive, evidence indicates that childhood hypopituitarism may be associated with a shortened adult lifespan, even with adequate hormonal replacement.
Is Panhypopituitarism curable?
It is treatable, and a patient with this condition should be able to perform normal activities as long as the appropriate hormonal therapy is used consistently and properly. Even after the proper regimen has been established, a patient with hypopituitarism requires lifelong medical follow-up.
Are Prolactinomas cancerous?
Prolactinoma is a noncancerous tumor of the pituitary gland. This tumor causes the pituitary gland to make too much of a hormone called prolactin. The major effect of a prolactinoma is decreased levels of some sex hormones — namely, estrogen and testosterone. A prolactinoma isn't life-threatening.
Can you get disability for pituitary tumor?
Pituitary disorders and pituitary tumors are deemed disabling conditions under Section 9.00 – Endocrine Disorders. It states that if any individual suffers from hormone production disruption, which affects the normal functioning of the other endocrine glands then such an individual qualifies for benefits.
What is panhypopituitarism?
Panhypopituitarism is a condition in which the production and secretion of all hormones by the pituitary gland is reduced. The pituitary gland, also called the “master gland of the body”, is a pea-sized organ located in the center of the brain. It produces and regulates the release of many different chemicals, or hormones, that control growth, sexual development and function, metabolism, and the body’s response to stress.
What is the goal of hypopituitarism treatment?
Treatment of hypopituitarism depends on its cause. The goal of treatment is to restore normal levels of hormones in the body.
What are some examples of pituitary hormones?
Some examples of pituitary hormones are: Growth hormone (GH): helps children grow in height and helps adults optimize fat and muscle development. This hormone also plays a role in the development and maintenance of bone strength. Thyroid stimulating hormone (TSH): Directs the thyroid gland in the neck to produce thyroid hormone, ...
Why is my pituitary hormone lowering?
Pituitary hormone production is regulated by the hypothalamus the area just above the pituitary that helps regulate hormone release from the gland. Reduced hormone output could be due to a problem with either the hypothalamus or the pituitary gland. Those problems, in turn, may be caused by: A tumor, or cyst, on or near ...
How to treat pituitary tumors?
Surgeons may reach the tumor through an incision in the upper lip or at the bottom of the nose, or by cutting through the skull. Radiation therapy may be used to kill tumor cells or to keep them from growing. Radiation therapy for a pituitary tumor must be narrowly targeted to minimize damage to nearby brain tissue.
Can panhypopituitarism be determined?
Sometimes, no exact cause of panhypopituitarism can be determined.
Can hormone replacement therapy help with panhypopituitarism?
Outlook. For most children and adolescents with panhypopituitarism , treatment with hormone replacement therapy is effective in restoring normal hormone levels. Hormone replacement therapy substitutes medically administered hormones for those normally produced by the pituitary gland. Even if the underlying cause of panhypopituitarism cannot be found ...
What diseases are associated with panhypopituitarism?
Infiltrative diseases such as hemochromatosis, sarcoidosis, and histiocytosis may be associated with the development of panhypopituitarism. Pituitary apoplexy is a medical emergency and is due to acute ischaemic infarction or hemorrhage of the pituitary gland. Pituitary apoplexy may occur in the presence of a pituitary adenoma ...
What causes panhypopituitarism?
Other causes of panhypopituitarism include injury to the pituitary gland following traumatic brain injury or iatrogenically during surgery or cranial irradiation. Inflammatory conditions of the pituitary may also be responsible for the occurrence of panhypopituitarism.
What are the symptoms of pituitary tumors?
Presenting signs and symptoms may be linked to that of a deficiency of pituitary hormone, mass effects in the presence of pituitary tumors, and/or features of the causative disease. Mass effects include visual field defects known as bitemporal hemianopsia. Visual field defects may also occur unilaterally. Patients may also present with headaches, secondary to the mass lesions. Manifestations that suggest congenital anterior hypopituitarism include micropenis, midline defects, optic atrophy, hypoglycemia, and poor growth 4). The presence of a secretory pituitary tumor may result in features of hormone excess for the particular hormone produced by a tumor while other pituitary hormones may be deficient 5).
How much of the pituitary needs to be damaged to result in panhypopituitarism?
Panhypopituitarism symptoms. It appears that that 75% of the pituitary needs to be damaged to result in panhypopituitarism. Clinical features of panhypopituitarism are diverse and may be subtle and ill-defined or severe with the acute presentation.
Can pituitary tumors cause acromegaly?
Pituitary tumors may cause the increased production of one hormone with resultant deficiency of the other pituitary hormones as in acromegaly (excess growth hormone with panhypopituitarism from the macroadenoma). Most pituitary tumors are benign and may be secretory or non-secretory.
How do you know if you have panhypopituitarism?
Other general symptoms of panhypopituitarism are hypersensitivity to cold, decreased appetite, anemia, infertility, loss of pubic hair , lack of body hair, facial swelling, inhibited sexual desire, etc. Excessive thirst and exaggerated increase in urine secretion may also occur, which come from diabetes insipidus.
What is hypopituitarism and panhypopituitarism?
The terms hypopituitarism and panhypopituitarism are sometimes used interchangeably, although the latter concept usually refers to a total deficit of certain hormones produced by the anterior lobe of the pituitary.
What is a condition characterized by inadequate or absent production of hormones from the anterior pituitary?
He Panhypopituitarism Is a condition characterized by inadequate or absent production of hormones from the anterior pituitary.
Why is my child's stature low?
The absence of hormones produces different symptoms according to what they are. Thus, a lack of growth hormone (GH) causes low stature in children.
Can panhypopituitarism cause short stature?
Some of them are short stature, low blood pressure, dizziness, muscle weakness, micropenis, optic atrophy, hypoglycemia, dry skin, fatigue, constipation, etc. However, these symptoms depend on the hormones that are affected and will vary if the condition is congenital or acquired. Panhypopituitarism can have multiple causes.
Can panhypopituitarism be removed?
In cases in which there are tumors that have produced panhypopituitarism, surgery is necessary to remove them. While, if the pituitary is under pressure, it can be opted for a decompression of the latter through transsphenoidal surgery (bypassing the Sphenoid bone ). This last treatment is the most appropriate to treat pituitary apoplexy.
Is hypopituitarism rare?
Both hypopituitarism and panhypopituitarism are very rare conditions. There are really few studies that examine the prevalence of this condition. Most are focused on hypopituitarism in general. According to Bajo Arenas (2009), the prevalence of hypopituitarism is 45.5 out of 100 000.
How to know if you have hypopituitarism?
See your doctor if you develop any of the signs and symptoms associated with hypopituitarism. Contact your doctor immediately if signs or symptoms of hypopituitarism develop suddenly or are associated with a severe headache, visual disturbances, confusion or a drop in blood pressure.
What is hypopituitarism caused by?
Hypopituitarism has a number of causes. In many cases, hypopituitarism is caused by a tumor of the pituitary gland. As a pituitary tumor increases in size, it can compress and damage pituitary tissue, interfering with hormone production. A tumor can also compress the optic nerves, causing visual disturbances.
What causes hypopituitarism in children?
Severe loss of blood during childbirth, which may cause damage to the front part of the pituitary gland (Sheehan's syndrome or postpartum pituitary necrosis) In some cases, hypopituitarism is caused by a genetic mutation ( inherited). These mutations affect the pituitary gland's ability to produce one or more of its hormones, ...
What are the symptoms of a woman having a low sex drive?
Women may also have symptoms such as: Hot flashes. Irregular or no periods. Loss of pubic hair. An inability to produce milk for breast-feeding.
What is the best treatment for hypopituitarism?
If you have hypopituitarism, you'll likely need to take medication for the rest of your life. Medication helps replace the missing hormones, which helps control your symptoms.
Can hypopituitarism affect blood pressure?
Symptoms typically vary, based on which hormone or hormones you are missing. If you have hypopituitarism, you'll likely need to take medication for the rest of your life.
Can a GH deficiency cause short stature?
In children, GH deficiency may cause growth problems and short stature. Most adults who have GH deficiency don't have any symptoms, but for some adults it can cause:
What are the symptoms of hypopituitarism in children?
Other symptoms and signs include. weakness, headache, abdominal pain, low blood pressure, vision problems, facial swelling, hoarseness,
What causes hypopituitarism?
A pituitary tumor is sometimes the cause of hypopituitarism. Other causes can include surgery or trauma to the brain, including stroke, radiation treatment, infections of the brain, loss of blood during childbirth (Sheehan syndrome), genetic conditions that result in impaired pituitary hormone production, autoimmune inflammation ...
What is it called when all the pituitary hormones are affected?
When all the pituitary hormones are affected, the condition is known as panhypopituitarism. Isolated or partial hypopituitarism results when the production of one or more hormones is decreased. The symptoms are variable and depend on the severity of the condition and the number of hormones that are affected. Symptoms can include.
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.
How to teach patients about panhypopituitarism?
Patient education is an important part of nursing care for patients with panhypopituitarism. Nurses need to teach patients about the pituitary gland and the crucial role pituitary hormones play in homeostasis. Emphasize the need for lifelong hormone replacement therapy, increased glucocorticoid replacement preceding and/or during stressful events, and prompt medical attention as appropriate. Tell them that regular follow-up visits with a healthcare provider are essential to ensure adequate hormone replacement and to prevent excessive hormone replacement. Encourage all patients to wear a medical-alert tag. 1
Why is LR at risk for panhypopituitarism?
The excision of a pituitary tumor and radiation therapy placed LR at risk for panhypopituitarism due to damage of the pituitary gland and resulting deficiency of anterior pituitary hormones . Although the hypothalamus may still attempt to control the level of pituitary hormones by releasing and inhibiting hormones, the anterior pituitary can't respond appropriately. This means that blood levels of anterior pituitary hormones—FSH, LH, ACTH, TSH, GH, and prolactin—become deficient. Similarly, damage to the posterior pituitary gland inhibits the release of oxytocin and ADH.1
What diseases are associated with the pituitary gland?
Diseases of the pituitary gland include infections, infarction, pituitary adenomas, pituitary surgery (such as pituitary adenoma excision), and radiation therapy of pituitary adenoma . The excision of a pituitary tumor and radiation therapy placed LR at risk for panhypopituitarism due to damage of the pituitary gland and resulting deficiency ...
What is the term for the decreased secretion of one, a few, or all the anterior pituit?
Hypopituitarism refers to decreased secretion of one, a few (isolated or partial hypopituitarism), or all the anterior pituitary hormones, which is known as panhypopituitarism . 1,2 A rare disorder, panhypopituitarism affects fewer than 200,000 patients in the United States according to the National Institutes of Health. 3
What are the symptoms of TSH deficiency?
Signs and symptoms include fatigue, cold intolerance, anorexia, constipation, facial puffiness, dry skin, bradycardia, delayed relaxation phase of the deep tendon reflexes, and anemia, although some patients with TSH deficiency have few or no symptoms. 6. GH deficiency.
Does the hypothalamus control the anterior pituitary?
Although the hypothalamus may still attempt to control the level of pituitary hormones by releasing and inhibiting hormones, the anterior pituitary can't respond appropriately. This means that blood levels of anterior pituitary hormones—FSH, LH, ACTH, TSH, GH, and prolactin—become deficient.

Panhypopituitarism Causes
Panhypopituitarism Symptoms
- It appears that that 75% of the pituitary needs to be damaged to result in panhypopituitarism. Clinical features of panhypopituitarism are diverse and may be subtle and ill-defined or severe with the acute presentation. Conditions such as Sheehan’s syndrome/pituitary apoplexy, pituitary infection, hypophysitis and traumatic brain injury present with acute findings 3. Presenting signs …
Panhypopituitarism Diagnosis
- Laboratory investigations Initial testing involves baseline levels of pituitary hormones and hormones produced by target hormones. Due to the variation of hormone levels related to the time of day, season and pulsatile secretion of certain pituitary hormones, baseline levels may not be helpful. In this instance, dynamic function testing may be performed to confirm biochemical d…
Panhypopituitarism Treatment
- Management is dependent on the cause of panhypopituitarism. Initial treatment is to address the underlying cause of panhypopituitarism. Mass lesions may be removed surgically and other medical conditions treated accordingly. Many patients may require hormone replacement therapy. Adrenocorticotropic hormone (ACTH) deficiency: Corticosteroid replacement should be initiated …