Pituitary and Hypothalamic Disorders Flashcards
Pituitary disorders Anterior
Adenomas Prolactinoma Acromegaly Gigantism Panhypopituitarism
Pituitary disorders Posterior
SIADH
Diabetes Insipidus
ormones of the anterior pituitary
FSH LH ACTH TSH Prolactin GH (Growth hormone)
Mnemonic: FLAT PeG
Hormones of the posterior pituitary
ADH
Oxytocin
These hormones are manufactured in the hypothalamus
Pituitary Adenomas
Microadenoma:
tumor less than 10 mm in diameter
More common (Prolactinoma)
Macroadenoma:
Larger than 10 mm in diameter
May cause mass effect
Adenomas cause increased levels of prolactin, what is the function of prolactin?
Prolactin blocks gonadotropins FSH and LH
So adenoma can lead to amenorrhea, infertility, decreased libido, etc.
Medical treatment of Hyperprolactinemia
is with dopamine agonists
Cabergoline (Best tolerated)
Bromocriptine
Acromegaly
Acromegaly is almost always caused by a pituitary tumor.
Excess growth hormone
Most frequently occurs in ages 20-40
May also be associated with tumors of the pancreas or parathyroid glands
Best initial test to rule out/in acromegaly
IGF-1 level
Serum GH not suppressed following oral glucose load (75-100 g glucose)
MRI:Pituitary tumor in 90%
Acromegaly Treatment
Treatment of choice is surgical.
Transsphenoidal resection
Best medical therapy is cabergoline (oral)
Or ocreotide, lanreotide, pegvisomant (sub Q injections)
Gamma knife radiosurgery if fail transsphenoidal surgery
Hypopituitarism Etiology
Pituitary apoplexy Hemorrhage into the pituitary gland Sheehan’s syndrome Post partum pituitary ischemic necrosis Infiltration Sarcoid, hemochromatosis, TB, syphilis Non-functioning adenoma Trauma Stroke Mass effect
The hormone deficiency to develop with lack of a functioning pituitary
GH : 1st hormonal deficiency to develop
LH/FSH: 2nd
TSH: 3rd
ACTH: 4th
Pituitary apoplexy
Hemorrhage into the pituitary
Usually secondary to existing adenoma
Acute symptoms: headache, nausea, vomiting, altered mental status, low blood pressure, low blood glucose
may treat with surgery
Sheehan’s syndrome
Post partum ischemic necrosis of the pituitary
Secondary to hypotension, emboli, HELLP syndrome
Symptoms: Difficulty breastfeeding, extended amenorrhea
Best initial test for hypopituitary function is to check anterior pituitary hormones.
LH/FSH
IGF-1 or GH insulin response test
TSH
ACTH: Measured indirectly through cortisol levels
MRI
SIADH Syndrome of Inappropriate Antidiuretic Hormone
SIADH is characterized by euvolemic hyponatremia due to elevated ADH levels.
Reabsorption of excess fluid
Low sodium
Low serum osmolality
SIADH Work up and diagnosis
CMP Urine sodium and osmolality Urine sodium is inappropriately high (>20 mEg/L) with low serum sodium (<130) Evaluate medications CT of the head **Rule out SIADH producing cancers: CXR (small cell cancer of the lung) CT abdomen (pancreatic cancer)
Diabetes Insipidus
Diabetes Insipidus occurs due to lack of appropriate levels of ADH
Central:
Deficiency of ADH (vasopressin)
Resistance to ADH
Nephrogenic:
Defect in the kidney tubules that interferes with water reabsorption
Diabetes Insipidus Work up
comparison of urine and serum sodium levels. CMP (includes a serum sodium) Plasma osmolality Plasma ADH Urine sodium and osmolality Water deprivation test DDAVP test