Prolactin, Acromegaly & Pituitary Adenoma
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Questions and Answers

A 30-year-old female presents with secondary amenorrhea, galactorrhea, and persistent headaches. Initial prolactin levels are significantly elevated. After excluding pregnancy and medication-induced hyperprolactinemia, which of the following is the MOST appropriate next step in evaluating the cause of her symptoms?

  • Order a high-resolution MRI of the pituitary gland. (correct)
  • Administer a dopamine agonist and monitor prolactin levels.
  • Initiate thyroid hormone replacement therapy.
  • Perform a lumbar puncture to rule out meningitis.

A patient is diagnosed with a pituitary macroadenoma causing visual field defects and panhypopituitarism. Which of the following hormonal deficiencies would MOST likely present the GREATEST immediate threat to the patient's life if left untreated?

  • Thyroid-stimulating hormone (TSH) deficiency
  • Growth hormone (GH) deficiency
  • Luteinizing hormone (LH) and follicle-stimulating hormone (FSH) deficiency
  • Adrenocorticotropic hormone (ACTH) deficiency (correct)

A researcher is investigating the regulatory mechanisms of prolactin secretion. Which of the following substances is the PRIMARY inhibitory regulator of prolactin release from the anterior pituitary?

  • Thyrotropin-releasing hormone (TRH)
  • Dopamine (correct)
  • Growth hormone-releasing hormone (GHRH)
  • Corticotropin-releasing hormone (CRH)

A 45-year-old male presents with progressive acromegaly. Despite undergoing transsphenoidal surgery to remove the pituitary adenoma, his growth hormone (GH) and IGF-1 levels remain elevated. Which of the following represents the MOST appropriate next step in his management?

<p>Referral for stereotactic radiosurgery or fractionated radiation therapy. (C)</p> Signup and view all the answers

A patient with known panhypopituitarism is started on hydrocortisone replacement therapy. Which of the following instructions is MOST crucial to provide to the patient regarding their medication?

<p>Double the dose during periods of significant stress, such as illness or surgery. (A)</p> Signup and view all the answers

A 50-year-old male presents with new-onset erectile dysfunction, decreased libido, and fatigue. His lab results show low testosterone, normal to low FSH and LH, and elevated prolactin. After ruling out other causes of hyperprolactinemia, what is the MOST likely underlying etiology for his hormonal abnormalities?

<p>Prolactinoma (D)</p> Signup and view all the answers

Which of the following mechanisms BEST explains how a non-functioning pituitary adenoma can cause hypopituitarism?

<p>Compression of the pituitary stalk, interfering with hypothalamic hormone delivery. (C)</p> Signup and view all the answers

A 32-year-old female with a history of a large pituitary adenoma treated with surgery and radiation presents with persistent headaches, fatigue, and new-onset diabetes insipidus. Which of the following hormonal deficiencies is MOST likely responsible for her diabetes insipidus?

<p>Antidiuretic hormone (ADH) (C)</p> Signup and view all the answers

Clinically silent pituitary adenomas, despite often staining positive for Gonadotrophin histologically, typically do not secrete. In the rare instances when they do secrete, what are the potential clinical manifestations observed in premenopausal women?

<p>Ovarian hyperstimulation. (D)</p> Signup and view all the answers

Panhypopituitarism is characterized by a deficiency in most or all of the hormones secreted by the pituitary gland. Which of the following combinations represents the most clinically relevant anterior pituitary hormone deficiencies associated with this condition?

<p>ACTH, TSH, FSH/LH, and Growth Hormone (GH). (A)</p> Signup and view all the answers

Pituitary macroadenomas are often associated with hypopituitarism due to the pressure they exert on pituitary cells. Besides pituitary adenomas, which of the following factors can lead to pituitary hormone deficiency?

<p>Pituitary surgery, radiation therapy, infiltration, hypophysitis and injury (B)</p> Signup and view all the answers

Sheehan's syndrome is a specific cause of panhypopituitarism that results from ischemic necrosis of the pituitary gland. What is the primary event that leads to this ischemic necrosis in Sheehan's syndrome?

<p>Hypotension from postpartum hemorrhage. (C)</p> Signup and view all the answers

A patient presents with decreased muscle mass, increased fat mass, and decreased bone mineral density. Based on the information provided, which of the following hormonal deficiencies is MOST likely contributing to these signs and symptoms?

<p>Growth Hormone (GH) deficiency. (B)</p> Signup and view all the answers

A female patient is experiencing a notable decrease in lactation following childbirth. Which hormonal deficiency is most likely the primary cause of this clinical manifestation?

<p>Prolactin deficiency. (D)</p> Signup and view all the answers

In cases of ACTH deficiency leading to secondary adrenal insufficiency, the clinical presentation is primarily due to a lack of what hormone?

<p>Cortisol. (A)</p> Signup and view all the answers

Secondary adrenal insufficiency results from a deficiency in ACTH, impacting the adrenal gland's ability to produce cortisol and adrenal androgens. How does the clinical presentation of secondary adrenal insufficiency MOST distinctly differ from that of primary adrenal failure (Addison's Disease)?

<p>Almost exclusively manifesting as cortisol deficiency symptoms. (D)</p> Signup and view all the answers

A patient presents with fatigue, anorexia, and abdominal pain. Lab results reveal hyponatremia and hypoglycemia. Which hormonal deficiency is MOST likely causing these symptoms?

<p>Adrenocorticotropic hormone (ACTH) deficiency (A)</p> Signup and view all the answers

A patient with known secondary adrenal insufficiency is admitted to the hospital with severe hypotension and dehydration. What is the MOST likely cause of this adrenal crisis?

<p>Non-compliance with glucocorticoid replacement during an acute illness. (D)</p> Signup and view all the answers

A male patient reports decreased libido, erectile dysfunction, and fatigue. Which hormonal deficiency is MOST likely responsible for these symptoms?

<p>Gonadotrophin (FSH/LH) deficiency (A)</p> Signup and view all the answers

Which of the following signs is MOST indicative of adrenal crisis, a life-threatening complication of adrenal insufficiency?

<p>Cardiovascular collapse (shock) (A)</p> Signup and view all the answers

A young female patient presents with primary amenorrhea. Which of the following deficiencies could MOST likely be the cause?

<p>Gonadotrophin deficiency (A)</p> Signup and view all the answers

A 45-year-old male presents with fatigue, muscle weakness, and joint pain. His blood tests reveal low cortisol levels. Further investigation reveals that the issue originates in the pituitary gland. Which of the following is the MOST likely diagnosis?

<p>Secondary adrenal insufficiency due to ACTH deficiency (B)</p> Signup and view all the answers

A patient with a history of pituitary adenoma develops sudden, severe headache, visual disturbances, and cardiovascular collapse. Which of the following conditions is the MOST likely cause of their current presentation?

<p>Pituitary apoplexy leading to acute secondary adrenal insufficiency. (B)</p> Signup and view all the answers

Which of the following conditions is LEAST likely to be mistaken for gonadotrophin deficiency in the differential diagnosis of fatigue and low libido in a young male?

<p>Long-term use of high-dose corticosteroids (D)</p> Signup and view all the answers

A patient presents with a pituitary adenoma alongside pancreatic endocrine and parathyroid tumors. Which genetic syndrome is most likely associated with this presentation?

<p>Multiple endocrine neoplasia (MEN) type 1 syndrome (D)</p> Signup and view all the answers

A patient with known acromegaly exhibits persistent headaches and blurred vision. Which of the following additional findings would most strongly suggest macroadenoma-related compression of the optic chiasm?

<p>Bitemporal hemianopia (C)</p> Signup and view all the answers

A 45-year-old male presents with decreased libido, erectile dysfunction, and is found to have elevated prolactin levels. Which of the following etiologies would be LEAST likely to be the primary cause of his hyperprolactinemia?

<p>High-dose estrogen therapy for prostate cancer (C)</p> Signup and view all the answers

A 32-year-old female presents with secondary amenorrhea and galactorrhea. Her prolactin level is significantly elevated. After ruling out pregnancy and medication use, what is the next most appropriate step in evaluating the cause of her hyperprolactinemia?

<p>Perform an MRI of the pituitary (A)</p> Signup and view all the answers

In the diagnosis of acromegaly, which of the following test results would provide the strongest evidence supporting the diagnosis?

<p>Elevated growth hormone (GH) levels after an oral glucose tolerance test (OGTT) (C)</p> Signup and view all the answers

A researcher is studying the mechanism of action of dopamine on prolactin secretion. Which of the following statements BEST describes the role of dopamine in regulating prolactin secretion?

<p>Dopamine directly inhibits prolactin secretion from lactotroph cells. (D)</p> Signup and view all the answers

A patient presents with visual disturbances, headaches, and symptoms of hypopituitarism. Imaging reveals a lesion in the sella turcica. Which of the following lesions, based on its origin, would be LEAST likely to cause hypersecretion of a pituitary hormone?

<p>Craniopharyngioma (B)</p> Signup and view all the answers

A patient is diagnosed with acromegaly. Besides elevated IGF-1 levels, what other diagnostic finding is crucial for confirming that the source of the excess growth hormone is a pituitary adenoma rather than ectopic production?

<p>Lack of growth hormone suppression following an oral glucose load (C)</p> Signup and view all the answers

A 50-year-old male presents with symptoms suggestive of acromegaly. His initial IGF-1 level is borderline elevated. Which of the following is the MOST appropriate next step to confirm the diagnosis?

<p>Perform an oral glucose tolerance test (OGTT) with serial GH measurements (C)</p> Signup and view all the answers

A patient with a known prolactinoma is being treated with a dopamine agonist. Which of the following clinical findings would warrant the MOST urgent evaluation and potential adjustment of their treatment?

<p>Development of new visual field defects (B)</p> Signup and view all the answers

A patient with long-standing, untreated acromegaly is MOST at risk for developing which of the following complications?

<p>Cardiomyopathy (C)</p> Signup and view all the answers

Why would the presence of galactorrhea be a less common symptom in men with prolactinomas compared to premenopausal women?

<p>Men have less developed mammary gland tissue, making galactorrhea less apparent. (D)</p> Signup and view all the answers

Which of the following findings would be most suggestive of a pituitary stalk compression interfering with dopamine delivery, rather than a primary prolactinoma?

<p>Both C and D (E)</p> Signup and view all the answers

A patient with acromegaly undergoes transsphenoidal surgery for removal of a somatotroph adenoma. Postoperatively, their IGF-1 levels normalize, but they develop persistent diabetes insipidus. What is the most likely cause of this new complication?

<p>Damage to the posterior pituitary or hypothalamus during surgery. (A)</p> Signup and view all the answers

What is the MOST likely long-term consequence of untreated acromegaly that directly contributes to increased mortality?

<p>Cardiovascular disease, including hypertension and cardiomyopathy. (B)</p> Signup and view all the answers

A patient presents with symptoms suggestive of acromegaly. Which of the following diagnostic findings would be most indicative of this condition, considering the complexities of hormone regulation and feedback?

<p>Elevated levels of insulin-like growth factor 1 (IGF-1) that fail to suppress adequately following an oral glucose tolerance test. (A)</p> Signup and view all the answers

A young female patient is diagnosed with a prolactinoma. Considering the nuances of dopamine agonist therapy, which of the following statements represents the most comprehensive understanding of its mechanism and expected outcomes?

<p>Dopamine agonists primarily reduce prolactin secretion by binding to dopamine receptors on lactotroph cells, which often leads to tumor shrinkage over time and can restore ovulatory function and menstrual cycles; however, the timeline for prolactin normalization and tumor size reduction varies. (B)</p> Signup and view all the answers

In differentiating between Cushing's disease and ectopic ACTH production as causes of Cushing's syndrome, which of the following clinical and biochemical findings would most strongly suggest ectopic ACTH production?

<p>Markedly elevated ACTH levels with hypokalemia, hyperpigmentation, and resistance to dexamethasone suppression, coupled with identification of a tumor on chest CT. (A)</p> Signup and view all the answers

A 5-year-old child is diagnosed with Prader-Willi syndrome. Considering the endocrine abnormalities associated with this genetic disorder, which of the following hormonal deficiencies is most commonly observed and requires careful monitoring and management?

<p>Growth hormone deficiency, contributing to short stature and altered body composition. (B)</p> Signup and view all the answers

A patient with known Hashimoto's thyroiditis presents with worsening fatigue, weight gain, and cold intolerance despite being on a stable dose of levothyroxine for several years. Which of the following factors should be most carefully evaluated to optimize their thyroid hormone replacement therapy?

<p>Assessing the patient's adherence to levothyroxine therapy, evaluating potential drug interactions affecting levothyroxine absorption or metabolism, and checking for significant changes in body weight or composition. (B)</p> Signup and view all the answers

What is the primary mechanism of action of cabergoline in the treatment of prolactinomas?

<p>Agonist activity at dopamine receptors, inhibiting prolactin secretion from lactotroph cells. (A)</p> Signup and view all the answers

A patient with Cushing's disease undergoes pituitary surgery, but post-operative cortisol levels remain elevated. Which of the following medical therapies would be most appropriate to consider next, taking into account the various mechanisms by which hypercortisolism can be managed medically?

<p>Initiation of metyrapone or ketoconazole, which inhibit steroidogenesis in the adrenal glands, reducing cortisol synthesis. (C)</p> Signup and view all the answers

In the management of acromegaly, somatostatin receptor ligands (SRLs) are frequently used when surgery is not curative. Which of the following mechanisms underlies the therapeutic effect of SRLs in this context?

<p>SRLs bind to somatostatin receptors on the pituitary adenoma cells, inhibiting GH secretion and potentially reducing tumor size. (B)</p> Signup and view all the answers

A patient is diagnosed with central diabetes insipidus following a traumatic brain injury. Considering the complexity of vasopressin regulation, which of the following hormonal profiles would be most consistent with this diagnosis?

<p>Elevated serum osmolality with low or undetectable levels of vasopressin. (C)</p> Signup and view all the answers

A patient is suspected of having autonomous cortisol secretion from an adrenal adenoma. Which of the following test results would provide the strongest evidence for this diagnosis, reflecting the disruption of normal hypothalamic-pituitary-adrenal (HPA) axis feedback?

<p>Suppressed plasma ACTH levels with elevated serum cortisol levels that do not suppress with low-dose dexamethasone. (B)</p> Signup and view all the answers

Flashcards

Pituitary Hormone Excess

Conditions caused by excessive secretion of pituitary hormones.

Pituitary Hormone Deficiency

Conditions resulting from insufficient secretion of pituitary hormones.

Cardinal Symptoms

Main symptoms associated with pituitary hormone disorders, such as headaches or fatigue.

Pathophysiology

The study of functional changes in the body caused by hormone excess or deficiency.

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Differential Diagnosis

A process to distinguish between different diseases presenting similar symptoms.

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Adenohypophysis

The anterior lobe of the pituitary gland, responsible for most hormone production.

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Neurohypophysis

The posterior lobe of the pituitary gland, which stores and releases hormones.

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Prolactin Levels

Measurement of the hormone prolactin in the blood, elevated in certain disorders.

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Pituitary adenomas

Tumors in the pituitary gland that may not secrete hormones.

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Hypopituitarism

Deficiency in one or more hormones from the pituitary gland.

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Panhypopituitarism

A deficiency in most or all pituitary hormones.

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ACTH deficiency

Leads to secondary adrenal insufficiency affecting cortisol levels.

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Secondary Hypothyroidism

Result of TSH deficiency, leading to insufficient thyroid hormone levels.

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Growth Hormone Deficiency

Results in short stature and decreased muscle mass.

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Sheehan’s syndrome

Ischemic necrosis of the pituitary after postpartum hemorrhage.

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Hypogonadism

Result of LH and FSH deficiency, affecting reproductive functions.

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Hypogonadotropic Hypogonadism

A condition caused by deficiency in gonadotrophins (FSH and LH), leading to low sex hormone levels.

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Symptoms of ACTH Deficiency

Common signs include fatigue, anorexia, weight loss, low glucose, and hyponatraemia due to low cortisol.

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Adrenal Crisis

A severe, life-threatening condition due to adrenal insufficiency, often marked by cardiovascular collapse.

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Gonadotrophin Deficiency Symptoms

Fatigue, low libido, muscle loss, and amenorrhoea caused by low FSH and LH levels.

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Primary vs Secondary Adrenal Insufficiency

Primary (Addison's disease) directly affects adrenal glands; secondary is due to ACTH deficiency.

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Signs of Low Cortisol Levels

Includes weight loss, hypoglycaemia, hyponatraemia, cartilaginous calcification in men due to cortisol deficiency.

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Differentials for Deficiencies

Possible causes for deficiencies in cortisol or gonadotrophins include primary disorders, hypopituitarism, or long-term medications.

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Prolactinoma

A common type of pituitary adenoma that secretes prolactin.

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Hypersecretion

Excessive hormone production by pituitary adenomas.

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Hyposecretion

Deficiency of hormones from the pituitary or hypothalamus.

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Somatotroph Adenoma

A pituitary tumor causing excess Growth Hormone (GH), leading to acromegaly or gigantism.

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Acromegaly

Condition in adults from excess GH, characterized by enlarged features.

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Gigantism

Excess GH in children before epiphyseal plate closure, resulting in tall stature.

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IGF-1

Insulin-like Growth Factor 1, elevated in GH excess conditions.

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Cortisol and ACTH

Excess ACTH from a corticotroph adenoma can cause Cushing’s disease.

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Prolactin Effects

Increased levels lead to amenorrhea, galactorrhea in women, and sexual dysfunction in men.

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Thyrotroph Adenoma

A rare adenoma causing excess TSH and central hyperthyroidism.

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Diabetes Mellitus

A potential complication of acromegaly due to insulin resistance.

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Carpal Tunnel Syndrome

Nerve entrapment condition that can occur in acromegaly.

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Hyperprolactinemia

Elevated prolactin levels often resulting from lactotroph adenomas.

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Pressure Symptoms

Symptoms arising from pituitary tumor pressure on surrounding tissues.

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Mortality Increase

Acromegaly-associated risk leading to higher death rates from complications.

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Prader-Willi Syndrome

A genetic disorder causing obesity, intellectual disability, and short stature.

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Cushing's Disease

A condition caused by excess cortisol due to a pituitary adenoma.

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Gonadotrophin Disorders

Hormonal imbalances often tied to pituitary adenomas.

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Malnutrition

A state of poor nutrition, leading to various health issues including hormone imbalances.

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Dopamine Agonists

Medications used to treat prolactinomas by mimicking dopamine.

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Somatostatin Receptor Ligands

Medications that inhibit growth hormone release, used in acromegaly treatment.

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ACTH

Adrenocorticotropic hormone that stimulates cortisol production from the adrenal glands.

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Study Notes

Conditions Due to Excess/Deficiency of Pituitary Hormones

  • Pituitary hormones control many physiological processes
  • Dysfunction can lead to various conditions, ranging from mild to severe
  • Excessive or insufficient hormone levels result in distinct symptoms and signs

Learning Outcomes

  • Define pituitary hormone excess/deficiency conditions
  • Explain the pathophysiology of pituitary hormone excess/deficiency
  • List cardinal symptoms and signs of pituitary hormone excess/deficiency
  • Explain how symptoms and signs arise in pituitary hormone excess/deficiency
  • Develop a differential diagnosis for pituitary hormone excess/deficiency

Case Study

  • A 24-year-old woman presents with amenorrhea, beginning at age 13
  • Menstruation became regular at age 15, then irregular and ceased completely by age 23
  • Milky discharge from nipples noted two months prior to presentation
  • Review of systems reveals headaches, fatigue, depression, cold intolerance, and difficulty losing weight, associated with a previous pregnancy
  • No medications
  • Physical examination: normal skin, hair, pelvic examination, mature breasts, and bilateral milk expression

Case Study - Initial Evaluation

  • Pregnancy test: negative
  • Thyroid Stimulating Hormone (TSH): normal
  • Prolactin: 6000 mU/L (normal range 90-500 mU/L)

Pituitary Hormones

  • Distinct hormones secreted by the anterior (adenohypophysis) and posterior (neurohypophysis) pituitary lobes
  • Most pituitary hormones secreted by the anterior pituitary gland
  • Regulate various physiological processes, including stress, growth, reproduction, metabolism, and lactation
  • Pituitary damage can be acute or chronic (over time), varying in severity
  • Clinical presentation depends on the affected hormones and severity of damage

Diseases of the Pituitary

  • Tumours: Pituitary Neuroendocrine Tumours
    • Adenomas arising from anterior pituitary cells
    • Can be clinically silent or secretory (e.g., prolactinoma, corticotroph adenomas)
    • Can be part of larger syndromes like Multiple Endocrine Neoplasia (MEN) type 1
  • Non-pituitary lesions (e.g., craniopharyngiomas, Rathke's cleft cysts) arising from cell rests in or near the sella turcica
  • Infiltrative diseases (e.g., sarcoid, hemochromatosis)
  • Inflammatory lesions (e.g., hypophysitis)
  • Infections
  • Trauma, hemorrhage, metastases

Hormonal Consequences

  • Hypersecretion: Only pituitary adenomas (or fragments thereof) can hypersecrete hormones
  • Hyposecretion: Any pituitary or hypothalamic disease can cause a deficiency in any hormone produced by the anterior pituitary

Pituitary Hormone Excess

  • Hyperpituitarism: Defined as an excess of one or more hormones normally secreted by the pituitary gland
  • Primarily relates to a single hormone
  • Clinically significant anterior pituitary excesses
    • Prolactin
    • Growth Hormone (GH)
    • Adrenocorticotropic Hormone (ACTH)
    • Thyroid Stimulating Hormone (TSH)
    • Follicle-stimulating Hormone (FSH) and Luteinizing Hormone (LH) - rare

Growth Hormone Excess (Acromegaly/Gigantism)

  • Excess GH causes:
    • Gigantism (childhood, before epiphyseal closure): longitudinal bone growth, resulting in tall stature and long extremities
    • Acromegaly (adults): enlargement of bones and soft tissues, particularly in the hands, feet, face, and head

Growth Hormone Excess (Acromegaly/Gigantism) - Clinical Presentation

  • Frontal bossing, coarsened facial features, prognathism, enlarged hands/feet/tongue, thickened skin, hyperhidrosis, skin tags
  • Nerve entrapment (e.g., carpal tunnel syndrome)
  • Associated symptoms (e.g., headaches, blurred vision, bitemporal hemianopia, diplopia) indicative of a pituitary mass
  • May present due to other pituitary hormone deficiency

Growth Hormone Excess (Acromegaly/Gigantism) - Diagnosis

  • Elevated serum insulin-like growth factor 1 (IGF-1)
  • Lack of growth hormone suppression after an oral glucose load

Pituitary Hormone Excess - Prolactinomas

  • Lactotroph cells secrete prolactin, leading to hyperprolactinemia, the most common pituitary adenoma
  • Clinical presentation varies by gender
    • Premenopausal women: amenorrhea or oligomenorrhea, galactorrhea
    • Postmenopausal women: pressure symptoms
    • Men: Decreased libido, decreased fertility, erectile dysfunction, galactorrhea, pressure symptoms

Prolactin

  • Under tonic inhibition by dopamine released from the hypothalamus
  • Elevated prolactin is common in hypothalamic-pituitary lesions (stalk effect)
  • Low prolactin can indicate severe hypopituitarism

Causes of Hyperprolactinemia

  • Physiological (pregnancy, lactation, exercise)
  • Pathological (lactotroph adenomas, pituitary stalk compression, medications like antipsychotics, gastric motility drugs, high-dose estrogens)

Pituitary Hormone Excess - ACTH/Thyrotroph

  • Corticotroph adenoma: Causes Cushing's disease due to excess ACTH
  • Thyrotroph adenoma: rare, causes central hyperthyroidism due to excess TSH

Gonadotroph Adenomas

  • Excess gonadotrophin secretion (FSH & LH) is rare
  • Often clinically silent, but may result in premature puberty (boys) and ovarian hyperstimulation (women)

Pituitary Hormone Deficiency – Hypopituitarism

  • Hypopituitarism: Defined as a deficiency in one or more hormones produced by the pituitary gland
  • Panhypopituitarism: Deficiency in most/all pituitary hormones
  • Anterior pituitary deficiencies
    • ACTH
    • TSH
    • FSH and LH
    • Growth hormone
  • Posterior pituitary deficiencies
    • Vasopressin (ADH) (will be taught later)

Pathophysiology of Pituitary Hormone Deficiency

  • Tumours (adenomas, cysts, metastatic cancer)
  • Pituitary surgery
  • Radiation therapy
  • Infiltration (hypophysitis)
  • Injury/trauma (e.g., Sheehans syndrome, post-partum hemorrhage)

Hypothalamic-Pituitary Deficiency Symptoms

  • Growth Hormone Deficiency: short stature, decreased muscle mass, increased fat mass, decreased bone mineral density
  • Prolactin Deficiency: decreased lactation
  • ACTH Deficiency: hypocortisolism
  • TSH Deficiency: secondary hypothyroidism
  • LH/FSH Deficiency: hypogonadism

Pituitary Hormone Deficiency - Specific Deficiencies

  • ACTH Deficiency: secondary adrenal insufficiency, nonspecific symptoms potentially delaying diagnosis
  • TSH Deficiency: secondary hypothyroidism
  • Gonadotrophin Deficiency: Hypogonadotropic hypogonadism (secondary hypogonadism)

Pituitary Hormone Deficiency - Diagnostic Considerations

  • Cortisol: Primary (Addison's) or secondary adrenal insufficiency, medications (long-term steroids)
  • Thyroid Stimulating Hormone (TSH): Primary, Secondary/Tertiary (hypothalamic) hypothyroidism, Hypopituitarism.
  • Growth Hormone (GH): Hypopituitarism, Syndromes (Prader-Willi, Turner syndrome), Malnutrition, Chronic disease, Medications (long-term steroids)
  • Gonadotrophins: Hypopituitarism, Kallmann syndrome

Hormone Active Pituitary Adenomas - Treatment

  • Prolactinomas: Dopamine agonists (Cabergoline, bromocriptine)
  • Acromegaly: Pituitary surgery, medical therapy (somatostatin receptor ligands, GH receptor blocker), radiation therapy
  • Cushing's Disease: Pituitary surgery, medical therapy (metyrapone, pasireotide, mifepristone, ketoconazole), radiation therapy, bilateral adrenalectomy

Case Study Summary

  • Prolactin levels: significantly elevated
  • Therapy: Cabergoline 0.5mg weekly initiated
  • Outcome: Normalization of prolactin at 2 months, resumption of menstruation, resolution of galactorrhea

Resources

  • Several online resource links for further study provided, about various pituitary conditions (e.g., hypopituitarism)

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Questions focus on diagnosing and managing pituitary disorders, including hyperprolactinemia and acromegaly. Covers appropriate diagnostic steps, life-threatening hormonal deficiencies, and regulatory factors.

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