Endo - Pathology (Pituitary) Flashcards

Pg. 324-236 in First Aid 2014 Sections include: -Pituitary adenoma -Acromegaly -Diabetes insipidus -SIADH -Hypopituitarism

1
Q

What is the most common pituitary adenoma? Is it benign or malignant?

A

Most commonly prolactinoma (benign)

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2
Q

What are the 2 general types of adenoma?

A

Adenoma may be functional (hormone producing) or nonfunctional (silent)

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3
Q

What is the main way in which nonfunctional adenomas present, and what are 3 effects that this presentation may have?

A

Nonfunctional tumors present with mass effect (bitemporal hemianopia, hypopituitarism, headache)

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4
Q

On what is the presentation of functional adenomas based? Give 2 examples of functional adenomas and their majors signs/symptoms.

A

Functional tumor presentation is based on hormone produced (e.g., Prolactinoma: amenorrhea, galactorrhea, low libido, infertility; Somatotropic adenoma: acromegaly)

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5
Q

What is the treatment for prolactinoma? What are 2 examples?

A

Treatment for prolactinoma: dopamine agonists (bromocriptine or cabergoline)

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6
Q

What defines Acromegaly? What typically causes it?

A

Excess GH in adults. Typically caused by pituitary adenoma

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7
Q

What are 5 signs/symptoms of Acromegaly?

A

(1) Large tongue with deep furrows (2) Deep voice (3) Large hands and feet (4) Coarse facial features (5) Impaired glucose tolerance (insulin resistance)

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8
Q

What are 3 ways in which Acromegaly can be diagnosed?

A

(1) High serum IGF-1 (2) Failure to suppress serum GH following oral glucose tolerance test (3) Pituitary mass seen on MRI

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9
Q

What is the first-line treatment for acromegaly? What are 2 options in the event that this does not work?

A

Pituitary adenoma resection. If not cured, treat with octreotide (somatostatin analog) or pegvisomant (growth hormone receptor antagonist)

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10
Q

What condition does excess GH in children cause, and why?

A

Excess GH in children => Gigantism (increased linear bone growth)

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11
Q

What is the most common cause of death in the context of gigantism?

A

Cardiac failure most common cause of death

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12
Q

What 3 major clinical findings characterize diabetes insipidus, and what are 2 causes of it?

A

Characterized by intense thirst and polyuria with inability to concentrate urine due to lack of ADH (central) or insensitivity to ADH (nephrogenic). Has a central or nephrogenic cause.

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13
Q

What are 6 possible etiologies of central DI?

A

(1) Pituitary tumor (2) Autoimmune (3) Trauma (4) Surgery (5) Ischemic encephalopathy (6) Idiopathic

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14
Q

What are 4 possible etiologies of nephrogenic DI?

A

(1) Hereditary (ADH receptor mutation), secondary to (2) hypercalcemia, (3) lithium, (4) demeclocycline (ADH antagonist)

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15
Q

Distinguish central versus nephrogenic DI in terms of the following lab findings: (1) ADH levels (2) Urine specific gravity (3) Serum osmolarity (4) Volume contraction.

A

(1) CD: low ADH; ND: normal ADH levels (2) CD & ND: urine specific gravity < 1.006 (3) CD & ND: Serum osmolarity > 290 mOsm/L (4) CD & ND: Hyperosmotic volume contraction

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16
Q

Describe the method of diagnosis for diabetes insipidus. How is central versus nephrogenic DI distinguished in diagnosis?

A

Water restriction test: No water intake for 2-3 hr followed by hourly measurements of urine volume and osmolarity and plasma Na+ concentration and osmolarity. DDAVP (ADH analog) is administered if normal values are not clearly reached; CENTRAL DI - Water restriction test: > 50% increase in urine osmolarity; NEPHROGENIC DI - Water restriction test: no change in urine osmolarity

17
Q

What are treatments for central versus nephrogenic DI?

A

CENTRAL DI: (1) Intranasal DDAVP (2) Hydration; NEPHROGENIC DI: (1) HCTZ (2) Indomethacin (3) Amiloride (4) Hydration

18
Q

What is SIADH? What are 3 major signs/symptoms that it causes?

A

Syndrome of inappropriate antidiuretic hormone secretion: (1) Excessive water retention (2) Hyponatremia with continued urinary Na+ excretion (3) Urine osmolarity > serum osmolarity

19
Q

What causes the hyponatremia in SIADH? What 2 major effects can hyponatremia have? How must it be corrected, and why?

A

Body responds to water retention with low aldosterone (hyponatremia) to maintain near-normal volume status. Very low serum sodium levels can lead to cerebral edema, seizures. Correct slowly to prevent central pontine myelinolysis.

20
Q

What are 4 causes of SIADH?

A

Causes include: (1) Ectopic ADH (small cell lung cancer) (2) CNS disorders/head trauma (3) Pulmonary disease (4) Drugs (e.g., cyclophosphamide)

21
Q

Give an example of ectopic ADH that may cause SIADH. Also, give an example of a drug that may cause SIADH.

A

Ectopic ADH (small cell lung cancer); Drugs (e.g., cyclophosphamide)

22
Q

What is the treatment for SIADH?

A

Treatment: (1) Fluid restriction (2) IV hypertonic saline (3) Conivaptan (4) Tolvaptan (5) Demeclocycline

23
Q

What is hypopituitarism? What are 5 causes of it?

A

Undersecretion of pituitary hormones due to: (1) Nonsecreting pituitary adenoma, craniopharygioma (2) Sheehan syndrome (ischemic infarct of pituitary following postpartum bleeding; usually presents with failure to lactate) (3) Empty sella syndrome (atrophy or compression of pituitary, often idiopathic, common in obese women) (4) Brain injury, hemorrhage (pituitary apoplexy) (5) Radiation

24
Q

What are 2 types of tumors that can cause hypopituitarism?

A

(1) Nonsecreting pituitary adenoma (2) Craniopharyngioma

25
Q

What is Sheehan syndrome? How does it usually present? What condition does it cause?

A

Sheehan syndrome (ischemic infarct of pituitary following postpartum bleeding; usually presents with failure to lactate); Hypopituitarism

26
Q

What defines empty sella syndrome? What often causes it? In what patient population is it common? What condition does it cause?

A

Empty sella syndrome (atrophy or compression of pituitary, often idiopathic, common in obese women)

27
Q

What are 2 brain insults that can cause hypopituitarism? What is a specific name for one when it specifically pertains to pituitary?

A

Brain injury, hemorrhage (pituitary apoplexy)

28
Q

What is the treatment for hypopituitarism?

A

Treatment: hormone replacement therapy (corticosteroids, thyroxine, sex steroids, human growth hormone).