pituitary & hypothalamus Flashcards

(58 cards)

1
Q

what is hypopituitarism

A

low functioning pituitary gland
*either a problem with the hypothalamus upstream OR pituitary gland itself

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2
Q

What are the causes of hypopituitarism

A

Hypothalamus or pituitary lesions
*pituitary adenoma

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3
Q

What type of adenoma is most common cause of hypopituitarism

A

prolactinomas

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4
Q

What age group is at highest risk for pituitary adenomas

A

30-40
*can be inherited

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5
Q

How does hypopituitarism present

A

Headaches /visual changes (mass effect)
-fatigue, dizziness, hypotension, confusion, polydipsia

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6
Q

If someone has GH deficiency, how will they present

A

short stature
micropenis
central obesity
hyperlipidemia
reduced muscle/bone mass
CV dysfunction

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7
Q

If someone has a gonadotropin deficiency, how will they present

A

FSH and LH deficiency
*hypogonadism and infertility, impaired/absent puberty, sexual dysfunction, loss of secondary male characteristics

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8
Q

how is hypopituitarism diagnosed

A

through evaluation of hormone levels or downstream effects
-evaluation of GH level

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9
Q

How can you evaluate GH levels

A

Via stimulation testing
*no GH increase w/ exercise
*no GH increase with glucagon

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10
Q

How can you test for adrenal deficiency

A

Low AM serum cortisol
Low serum ACTH
Low serum DHEA
Low ACTH w/ cosyntropin stimulation

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11
Q

What type of imaging is done to assess the pituitary

A

MRI of hypothalamus

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12
Q

Who will have an MRI of their hypothalamus to assess the pituitary

A

Men>16 with low LH & serum testosterone.

2+ pituitary hormone deficiencies

Persistent hyperprolactinemia

symptoms of mass effect

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13
Q

What will be seen on imaging with hypopituitarism

A

Distinct mass
generalized pituitary enlargement
thickening of pituitary stalk

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14
Q

How do you treat hypopituitarism

A

Resection of tumors or other masses

dopamine agonist in prolactinomas (first line)

radiation as a last line

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15
Q

What are the dopamine agonists used for prolactinomas

A

bromocriptine or cabergoline

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16
Q

If the pituitary gland is removed, what does the patient need to take for the rest of their life

A

-Glucocorticoid replacement (hydrocortisone)

-levothyroxine AFTER glucocorticoid initiation

-Gonadotropin replacement

-hGH replacement

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17
Q

what is a pituitary adenoma

A

Benign tumor arising from any one of the pituitary cell types

*most common cause of hypo and hyperpituitarism in adults

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18
Q

What are the classifications of pituitary adenomas

A

Micro vs Macro
Functioning vs Non-functioning

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19
Q

What is a functioning pituitary adenoma

A

secretion of hormones by the tumor

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20
Q

What is a macro adenoma

A

> 1cm diameter -> generally get mass effect and hypopituitarism

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21
Q

What is the test of choice for a pituitary adenoma

A

MRI with gadolinium

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22
Q

What is a secondary hormone dysfunction workup

A

Basal prolactin
insulin like growth factor
24hr urinary free cortisol
FSH & LH
Thyroid function test

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23
Q

What are acidophils

A

GH
Prolactin

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24
Q

What are basophils

A

TSH
LH/FSH
ACTH

25
If the pituitary adenoma is small, how do you treat
Annual MRI to monitor *if no growth, can reduce frequency
26
How do you treat a macro adenoma
Resection via a transsphenoidal approach +/- radiation
27
What medications can inhibit a pituitary adenoma
Somatostatin dopamin *both inhibit
28
what is the most common pituitary hormone hypersecretion syndrome
Hyperprolactinemia
29
What are the underlying causes of hyperprolactinemia
Physiologic: exercise, inherited, sleep Pharmacologic: amphetamines, opioids, nicotine, TCA, SSRI Pathologic: Acromegaly, Hypothalamic disease, hypothyroidism, tumors
30
What is a normal prolactin level in males
<20ng/mL
31
What is a normal prolactin level in non-pregnant women? Pregnant?
<25ng/mL 40-800ng/mL
32
What prolactin levels are indicative of a prolactinoma (excluding pregnancy)
>200ng/mL
33
How do you workup hyperprlactinemia
Evaluate for underlying causes (test all other pituitary hormones) If no physiological change or pharmacologic cause -> MRI
34
What is gigantism
excessive growth in childhood, prior to physical closure (long bones)
35
What is acromegaly
excessive growth after physical closer (no long bone involvement) -hands -feet -head
36
How do you test for acromegaly and gigantism
Random serum IGF-1 *if normal= ruled out
37
How is gigantism physically differentiated from acromegaly
They have a tall stature and delayed puberty, where as acromegaly the bones would be wider than normal
38
What is the workup for acromegaly and gigantism
Fasting, no exercise, and no illness -serum IGF-1 -prolactin level -Glucose -LFTs,BUN,creatinine -serum calcium -free T4 and TSH
39
What kind of imaging can be done for acromegaly and gigantism
pituitary MRI Skull xray (enlarged sella, thick skull) Xray of hand and feet
40
What will be seen on the hand and feet X-rays with acromegaly
tufting of phalanges (spade looking) Enlarged calcaneous
41
What is the treatment of choice for acromegaly and gigantism
Transsphenoidal resection
42
What is the most common skeletal dysplasia
achondroplasia
43
What type of genetic disease is achondroplasia
Autosomal dominant fibroblast GF receptor 3 gene *if homozygous = Letha;
44
What are some clinical features of achondroplasia
Disproportionate short stature large head delayed motor development short fingers exagg. lumbar lordosis prominent forehead
45
How can achondroplasia be confirmed
genetic testing +FGFR3 mutation
46
What complications arise from achondroplasia
recurrent OM OSA Obesity spinal stenosis narrow foramen magnum (can cause hydrocephalus)
47
What is Diabetes insipidus
deficiency in ADH (vasopressin) - posterior pituitary loss of renal H2O reabsorption = polyuria
48
What are the types of diabetes insipidus
Central (ADH deficiency) - primary cause being no lesion Nephrogenic (kidney just isn't responding to ADH)
49
What is the presentation of diabetes insipidus
intense thirst cravings for ice water polyuria enuresis
50
If urine has high volume and low specific gravity, how is it classified
dilute
51
What testing can rule of DI
24hr urine collection with less that 2L collected
52
How do you treat diabetes insipidus
DDAVP (desmopressin) Nasal, SQ or IV (nasal / oral preferred) start low and go slow
53
What is SIADH
Inappropriate release of ADH
54
Who is at increased risk for DI
Pituitary tumor Craniotomy head injury
55
What causes SIADH
Central (metabolic, CNS, psychiatric, iatrogenic) Lungs (infection, mechanical, tumors- specifically small cell)
56
How does SIADH present
decreased fluid output even with adequate or increased intake *fluid overload-> edema, hyponatrema, BP
57
What would workup show with SIADH
Serum hyponatremia hypoosmolality increased urine sodium concentration normal thyroid/adrenal function
58
What is the treatment of SIADH
Treat underlying causes fluid restriction*** if severe -> IV sodium chloride