pituitary Flashcards

1
Q

pituitary space occupying lesions can cause underproduction and overproduction what are examples of each

A

underproduction: hypopituitarism

overproduction:
1) gh-> (gigantism before fusion of epiphysis)
(acromegaly after fusion of epiphysis)
2) prolactin -> galactohrrhea, amenhorrea, erectile dysfunction
3) ACTH –> cushings disease
4) TSH-> hyperthyroidism

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2
Q

if a pituitary tumor is in optic chiasm what would happen

A

bitemporal hemianopia

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3
Q

if pituitary tumor in cavernous sinus

A

CN 3,4,6
ooculomotor
abducens
trochlear

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4
Q

what are symptoms in a patient with a tumor compressing cavernous sinus

A

3- ptosis, diplopia, pupil dilation
4- vertical diplopia difficulty looking downward
6- lateral rectus palsy- inability to abduct the eye

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5
Q

tumor in hypothalamic centers symptoms

A

obesity
altered apetite and thirst
precocious puberty

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6
Q

diff btwn microadenoma and macroadenoma

A

micro: <1cm (prolactin lvl and yearly MRI)
macro: > 1cm (prolactin lvl, yearly mri, TSH T4 LH FSH IGF )

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7
Q

what type of surgery is gold standard for pituitary tumors especially macroadenomas

A

transphenoidal surgery enter thru the sphenoid sinus

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8
Q

almost all pituitary tumors are malignant
T or F

A

false. most are benign

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9
Q

hypopituitarism meaning

A

low hormones produced in pituitary

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10
Q

causes of hypopituitarism

A

1)pituitay or hypothalamic tumor (compression-necrosis-dec hormone )
2)previous surgery /radiation of pituitary adenoma
3) sheehan syndrome, infiltrative process

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11
Q

clinical features of hypopituitarism depending on each hormone

A

GH- short stature in children, silent in adults, inc LDL, inc risk of heart disease
LH and FSH- loss of libido, amenorrhea, erectile dysfunction
ACTH- hypotension ( secondary adrenal insufficiency)
TSH- fatigue and tiredness (secondary hypothyroidism)
prolactin- no lactate
ADH- diabetes insipidus
MSH- dec skin and hair pigment

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12
Q

most likely cause of compression of pituitary in adults and children

A

in adults: pituitary tumor/adenoma
in children: craniopharyngiomas from rathkes pouch develop in anterior pituitary

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13
Q

what is cause of pituitary apoplexy

A

1) hemorrhage : often due to pituitary adenoma, benign tumor demand more blood so more pressure
2) infarction: sheehans syndrome during preg high demand for blood by pituitary cells and escessive blood loss during childbirth , pituitary cells die if not restored

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14
Q

what are symptoms of FSH and LH in hypopituitarism

A

in women : oligomenhorrea, amenhorrea, infertility
men : loss of pubic hair , reduce muscle mass

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15
Q

in hypopituitarism which hormones are depleted first

A

LH, FSH, GH

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16
Q

tx of hypopituitarism

A

hormone replacement therapy
tumor removal

17
Q

what is kalman syndrome

A

it is a rare genetic conditions occurs due to defective migration of GnRH-releasing neurons from olfactory bulbs to hypothalamic preoptic nuclei +complete loss of smell

dec GnRH secretion and underdeveloped olfactory bulbs
dec GnRH
dec pituitary secretion of FSH LH
dec testosterone in male
dec estrogen Female

18
Q

what does it show on imaging of sheehan syndrome

A

empty sella turcica

19
Q

what is when pituitary gland is either located eccentrically or in some ppl pituitary atrophy

A

empty sella syndrome

20
Q

what is a primary and secondary form of empty sella syndrome

A

primary: enlarged or malformed of sella turcica which surround pituitary gland so csf leaks in and fill sella turcica –> compression or atrophy of gland
secondary: small gland due to removal

21
Q

causes of hyperprolactinemia

A

1)adenoma of pituitary ( prolactinoma, most common type)
2)primary hypothyroidism ( inc in TRH –> stimulate prolactin secretion)
3)acromegaly ( prolactin co-secreted w GH)
4)PCOS- more estrogen more release of prolactin)
5)Drugs
6)compressed pituitary stalk by suprasellar mass lesion causing disassociation and discontinued of dopamine delivery to ant pituitary –> loss of inhibitory factor

22
Q

features of hyperprolactinemia

A

1)galactohrrea
2) hypogonadism: Female= amenorrhea, infertility, anovulation, dec libido, risk of osteoporosis
male=erectile dysfunction,dec libido, infertility,
3) headaches and visual defect

23
Q

what is the diagnosis of hyperprolactinema

A

1) perform serum prolactin first
2) thyroid function test
3) rule out pregnancy - B-HCG
4) Kidney and liver function - disease eelvate prolactin

24
Q

when is MRI done if hyperprolactinema is suspected

A

if high prolactin is confirmed
secondary causes excluded
patient not pregnant

25
what is the treatment options in prolactinoma
medical is #1 sugical #2 However, in acromegaly #1 surgical #2 medical
26
what is MEDICAL tx for hyperprolactinema
dopamine agonists : cabergoline and bromocriptine
27
what is SURGICAL tx of hyperprolactinemia
transphenoidal resection of pituitary adenoma appropriate if no response from medications
28
if a female patient comes in with high prolactin what is one thing you should always exclude
pregnancy
29
what is the most common cause of death in pts with acromegaly
cardiomyopathy
30
Gh is secreted in what type of pattern
pulsatile pattern , in pulses mainly at night durimg deep sleep
31
Gh is secreted by what eans regulated by who
Regulation of GH secretion is by : GHRH -> stimulate GH release somatostatin-> inhibit ghrelin-> stimulate
32
GH has direct effects on metabolism which are
inc fat breakdown dec glucose uptake by cells inc protein synthesis
33
what does gh indirectly induce
IGF-1 - produced in liver in response to GH provides negative feedback to hypothalamus and pituitary to reduce GH secretion.
34
causes of acromegaly and gigantism
1) always Gh secreting pituitary adenoma 2) cound be associated with MEN1 when combined w parathyroid and pancreatic disorders
35
symptoms of excess GH production could be divided into
symptoms due to local mass effect symptoms due to excess GH or IGF-1
36
what it is the diagnosis of acromegaly and gigantism
initial test: serum IGF-1 ->> significantly elevated
37
what it is the most accurate test to know if pt has acromegaly or gigantism
oral glucose suppression test : glucose load fails to suppress GH as it should be in healthy individuals ( confirms if IGF-1 is uncertain)
38
what will lab tests show in patient with acromegaly
glucose intolerance and hyperlipidemia
39
what is tx of acromegaly or gigantism in medications
cabergoline: Dopamine agonist inhibit GH release octreotide: somatostatin inhibits GH relaese