PITUITARY ADENOMA Flashcards

1
Q

Define pituitary adenomas:

A

tumors that derive from one of the 5 types of pituitary hormone producing cells within the anterior lobe of pituitary
>95% are sporadic, <5% are genetic

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2
Q

what are the size classifications of pituitary adenomas?

A

microadenoma: <10 mm (functional)
macroadenoma: > or equal to 10 mm (mass effect)

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3
Q

how else are pituitary adenomas classified?

A

secretory and non-secretory

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4
Q

pituitary adenoma epidemiology:

A
  • most commonly dx btwn 30-60 y/o
  • > 60% benign, 30% invasive, <1% carcinomas
  • cause 60% all cases of hypopituitarism
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5
Q

pituitary adenoma pathophys:

A

growth of adenoma will compress surrounding glandular tissue
most adenomas will arise from a single pituitary cell type

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6
Q

what type of adenoma are 60% of all pituitary adenomas?

A

secretory adenomas

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7
Q

lactotroph adenomas

A

40%, most common
increased prolactin leads to hyperprolactinemia

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8
Q

somatotroph adenomas

what do they lead to

A

also most common
increased growth hormone leads to acromegaly or gigantism

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9
Q

corticotroph adenomas

what do they increase and lead to?

A

increased adrenocorticotropic hormone (ACTH) leading to cushings

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10
Q

thyrotroph adenomas

A

rare
increased TSH leads to 2ndary hyperthyroidism

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11
Q

what is the most common type of adenoma that is derived from multiple types of pituitary cells secreting more than 1 hormone?

A

somatotroph + lactotroph
often atypical and/or malignant forms of adenomas, which transform into aggressive and tx-resistant carcinomas

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12
Q

what are 40% of all pituitary adenomas?

A

non-secretory

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13
Q

> 80% of non-secretory cases derive from what type of cells of the pituitary

A

gonadotroph

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14
Q

definition of hypopituitarism:

A

decreased secretion of one, some, or all anterior pituitary hormones

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15
Q

what are the causes of hypopituitarism?

three things

A
  1. most common: adenoma
  2. infarct
  3. 2ndary sempty sella syndrome (head trauma, infxn, radiation therapy, pituitary surgery, Sheehan syndrome)
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16
Q

what is the pathophys of hypopituitarism?

A

destruction of >75% pituitary tissue resulting in sequential loss of anterior pituitary hormones.
sx depend on deficient hormones

17
Q

what are the most common pituitary hormone deficiencies?

A

gonadotropins resulting in hypogonadism in both men and women

18
Q

what is the clinical presentation of microadenomas <10?

A

non secretory is asymptomatic
secretory causes hyperpituitarism
- sx depend on effects that excessive hormone exerts on peripheral target organs
- hyperprolactinemia, acromegaly or gigantism, cushings, 2ndary hyperthyroidism

19
Q

what is the clinical presentation of non-secretory macroadenomas >or equal to 10?

A

MASS EFFECT SYMPTOMS
1. bitemporal hemianopsia- diminished vision in bilateral temporal fields
2. diplopia from compression of optic chiasma nerve
3. opthalmoplegia- paralysis of CN 3,4,6 (extraocular eye muscles); results from invasion of cavernous sinus
4. headache
5. vomitting w/o nausea
6. AMS
7. pituitary apoplexy- sudden loss of blood supply to pituitary gland, leading to tissue necrosis and loss of fxn d/t sudden hemorrhage into adenoma -> excruciating HA and diplopia

20
Q

what is the clinical presentation of secretory macroadenomas >or equal to 10?

A

hyperpituitarism
sx depend on hormone-specific effects
other hormones are deficient d/t pituitary tissue destruction
mass effect sx

21
Q

how are most microadenomas diagnosed?

A

incidentally

22
Q

what is clinical suspicion based on?

A

sx caused by excessive hormone in addition to mass effect symptoms.
this combo suggests pituitary mass

23
Q

what is the gold standard imaging to confirm sellar masses, size, and location?

A

contrast MRI
(CT used if MRI contraindicated-> pts w/ pacemaker or metallic implants)

24
Q

What laboratory testing is done?

A
  1. basal prolactin levels to assess prolactinomas
  2. insulin-like GF-1 levels to assess somatotroph adenomas
  3. 24 hr urine cortisol levels to assess corticotroph adenomas
  4. thyrotropin-releasing hormone, TSH, free T3 and T4 levels to assess thyrotroph adenomas
25
Q

pituitary adenoma management:

A

non-secretory microadenomas: no tx, f/u
secretory regardless of size: rq medical therapy to counteract hormonal effects
macroadenomas regardless of hormone production require surgical or radiation therapy to alleviate compression effects (increased intracranial pressure, visual disturbances, headaches)

26
Q

What is involved in adenoma surgical resection?

A

transphenoidal adenectomy (removal of adenoma) or complete/partial hypophysectomy (removal of pituitary) is used when medical therapy fails
pituitary irradiation can be used to supplement surgical resection
complications: post-op/post-radiation hypopituitarism -> requires life-long hormone replacement therapy

27
Q

what is a prolactinoma?

A

functional, usually benign lactotroph cell tumor in the anterior pituitary -> prolactinemia

28
Q

what is the most common type of pituitary tumor (adenoma) that accounts for 30% of all pituitary adenomas?

A

prolactinoma

29
Q

what can cause prolactinoma?

A

may occur as part of inherited condition called multiple endocrine neoplasia type 1 (MEN 1)

30
Q

signs and symptoms of prolactinoma?

A

women: galactorrhea, amenorrhea
men: gynecomastia, erectile dysfunction

31
Q

how is prolactinoma diagnosed?

A

with increased increased serum prolactin

32
Q

first line prolactinoma treatment?

A

dopamine agonists- to suppress prolactin secretion
- cabergoline ot bromocriptine

33
Q

memorize hormone slide

A