Podcast
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?
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?
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?
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?
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?
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?
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?
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?
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?
Which of the following mechanisms BEST explains how a non-functioning pituitary adenoma can cause hypopituitarism?
Which of the following mechanisms BEST explains how a non-functioning pituitary adenoma can cause hypopituitarism?
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?
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?
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?
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?
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?
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?
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?
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?
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?
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?
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?
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?
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?
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?
In cases of ACTH deficiency leading to secondary adrenal insufficiency, the clinical presentation is primarily due to a lack of what hormone?
In cases of ACTH deficiency leading to secondary adrenal insufficiency, the clinical presentation is primarily due to a lack of what hormone?
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)?
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)?
A patient presents with fatigue, anorexia, and abdominal pain. Lab results reveal hyponatremia and hypoglycemia. Which hormonal deficiency is MOST likely causing these symptoms?
A patient presents with fatigue, anorexia, and abdominal pain. Lab results reveal hyponatremia and hypoglycemia. Which hormonal deficiency is MOST likely causing these symptoms?
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?
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?
A male patient reports decreased libido, erectile dysfunction, and fatigue. Which hormonal deficiency is MOST likely responsible for these symptoms?
A male patient reports decreased libido, erectile dysfunction, and fatigue. Which hormonal deficiency is MOST likely responsible for these symptoms?
Which of the following signs is MOST indicative of adrenal crisis, a life-threatening complication of adrenal insufficiency?
Which of the following signs is MOST indicative of adrenal crisis, a life-threatening complication of adrenal insufficiency?
A young female patient presents with primary amenorrhea. Which of the following deficiencies could MOST likely be the cause?
A young female patient presents with primary amenorrhea. Which of the following deficiencies could MOST likely be the cause?
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?
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?
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?
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?
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?
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?
A patient presents with a pituitary adenoma alongside pancreatic endocrine and parathyroid tumors. Which genetic syndrome is most likely associated with this presentation?
A patient presents with a pituitary adenoma alongside pancreatic endocrine and parathyroid tumors. Which genetic syndrome is most likely associated with this presentation?
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?
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?
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?
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?
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?
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?
In the diagnosis of acromegaly, which of the following test results would provide the strongest evidence supporting the diagnosis?
In the diagnosis of acromegaly, which of the following test results would provide the strongest evidence supporting the diagnosis?
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?
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?
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?
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?
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?
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?
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?
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?
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?
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?
A patient with long-standing, untreated acromegaly is MOST at risk for developing which of the following complications?
A patient with long-standing, untreated acromegaly is MOST at risk for developing which of the following complications?
Why would the presence of galactorrhea be a less common symptom in men with prolactinomas compared to premenopausal women?
Why would the presence of galactorrhea be a less common symptom in men with prolactinomas compared to premenopausal women?
Which of the following findings would be most suggestive of a pituitary stalk compression interfering with dopamine delivery, rather than a primary prolactinoma?
Which of the following findings would be most suggestive of a pituitary stalk compression interfering with dopamine delivery, rather than a primary prolactinoma?
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?
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?
What is the MOST likely long-term consequence of untreated acromegaly that directly contributes to increased mortality?
What is the MOST likely long-term consequence of untreated acromegaly that directly contributes to increased mortality?
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?
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?
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?
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?
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?
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?
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?
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?
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?
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?
What is the primary mechanism of action of cabergoline in the treatment of prolactinomas?
What is the primary mechanism of action of cabergoline in the treatment of prolactinomas?
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?
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?
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?
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?
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?
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?
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?
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?
Flashcards
Pituitary Hormone Excess
Pituitary Hormone Excess
Conditions caused by excessive secretion of pituitary hormones.
Pituitary Hormone Deficiency
Pituitary Hormone Deficiency
Conditions resulting from insufficient secretion of pituitary hormones.
Cardinal Symptoms
Cardinal Symptoms
Main symptoms associated with pituitary hormone disorders, such as headaches or fatigue.
Pathophysiology
Pathophysiology
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Differential Diagnosis
Differential Diagnosis
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Adenohypophysis
Adenohypophysis
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Neurohypophysis
Neurohypophysis
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Prolactin Levels
Prolactin Levels
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Pituitary adenomas
Pituitary adenomas
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Hypopituitarism
Hypopituitarism
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Panhypopituitarism
Panhypopituitarism
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ACTH deficiency
ACTH deficiency
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Secondary Hypothyroidism
Secondary Hypothyroidism
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Growth Hormone Deficiency
Growth Hormone Deficiency
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Sheehan’s syndrome
Sheehan’s syndrome
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Hypogonadism
Hypogonadism
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Hypogonadotropic Hypogonadism
Hypogonadotropic Hypogonadism
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Symptoms of ACTH Deficiency
Symptoms of ACTH Deficiency
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Adrenal Crisis
Adrenal Crisis
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Gonadotrophin Deficiency Symptoms
Gonadotrophin Deficiency Symptoms
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Primary vs Secondary Adrenal Insufficiency
Primary vs Secondary Adrenal Insufficiency
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Signs of Low Cortisol Levels
Signs of Low Cortisol Levels
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Differentials for Deficiencies
Differentials for Deficiencies
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Prolactinoma
Prolactinoma
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Hypersecretion
Hypersecretion
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Hyposecretion
Hyposecretion
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Somatotroph Adenoma
Somatotroph Adenoma
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Acromegaly
Acromegaly
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Gigantism
Gigantism
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IGF-1
IGF-1
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Cortisol and ACTH
Cortisol and ACTH
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Prolactin Effects
Prolactin Effects
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Thyrotroph Adenoma
Thyrotroph Adenoma
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Diabetes Mellitus
Diabetes Mellitus
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Carpal Tunnel Syndrome
Carpal Tunnel Syndrome
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Hyperprolactinemia
Hyperprolactinemia
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Pressure Symptoms
Pressure Symptoms
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Mortality Increase
Mortality Increase
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Prader-Willi Syndrome
Prader-Willi Syndrome
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Cushing's Disease
Cushing's Disease
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Gonadotrophin Disorders
Gonadotrophin Disorders
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Malnutrition
Malnutrition
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Dopamine Agonists
Dopamine Agonists
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Somatostatin Receptor Ligands
Somatostatin Receptor Ligands
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ACTH
ACTH
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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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Description
Questions focus on diagnosing and managing pituitary disorders, including hyperprolactinemia and acromegaly. Covers appropriate diagnostic steps, life-threatening hormonal deficiencies, and regulatory factors.