HYHO - Newman #2 Flashcards

1
Q

the HPA axis is a neurodendocrine system that controls reactions to _ and regulates _ (X5)

A

stress

digestion, immune system, mood, sexuality, energy

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2
Q

the _ _ _ of the HPA axis helps to regulate the concentration of hormones in the blood thus preventing over or under correction

A

negative feedback system

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3
Q

what zone of the adrenal cortex is responsible for

mineralocorticoids
glucorticoids
sex steroids

A

mineralocorticoids- glomerulosa
glucorticoids- fasiculata
sex steroids- reticularis

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4
Q

short term stress response involves stimulation of the _ via the _ fibers resulting in the release of _

A

adrenal medulla

via preganglionic sympathetic ribers

catecholamines

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5
Q

example of short term stress reponses

A

increased HR
increased BP
glycogen conversion to glucose in the liver and release into the blood
changes in blood flow patterns: decrease digestive system activity and reduced urine output
increased metabolic rate

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6
Q

long term stress response involves _ stimulation from the _, stimulation of the adrenal cortex by _ and release of _ and _

A

CRH stimulation from the anterior pituitary

stumulation of the adnreal cortex by ACTH

and release of mineralocorticoids and glucocorticoids

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7
Q

what are mineralocorticoids? what do they do?

A

aldosterone that leads to retention of sodium and water by the kidneys

increased blood volume and blood pressure

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8
Q

what are the glucocorticoids? what do they do?

A

cortisol they convert proteins and fats to glucose or energy
lead to an increased blood glucose, and suppresion of the immmune system

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9
Q

the renin angiotension aldosterone system is important in the regulation of _ , _ , and _ physiology

A

renal, cardiac, vascular

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10
Q

renin secretion from the kidney is stimulated by?

A

decreased renal perfusion (decreased blood to the kidney) or increase sympathetic anctivity

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11
Q

angiotensiongen is converted to angiotensin I by _

angiotensin I is converted to angiotension II by _

angiotensin II stimulates _ release from the _

A

renin

angiotension converting enzyme

aldosterone

from the adrenal cortex

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12
Q

always _ the genitalial of a newborn baby

A

examine

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13
Q

the most common cause of ambiguous genitalial in a genetically female infant is?

A

congenital adrenal hyperplasia causing virilization of the genitalia

can be life threatening and must be thought of if a baby presents with ambigious geneitalila

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14
Q

what is the common def. in congeital adrenal hyperplasia

what is there an increase of

A

21-hydroylase def (increased testosterone)

increase of the precursor - 17-OH progesterone

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15
Q

symptoms of congeital adrenal hyperplasia in a neonate

A

failure to thrive, recurrent vomiting, dehydration, hypotension, hyponatermia, hyperkalamia, shock

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16
Q

most common cause of congeital adrenal hyperplasia and the effects it has on aldosterone, cortisol, and androgens

A

cause: 21 hydroxylase def

aldosterone: low
cortisol: low
androgens: high

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17
Q

what are the mainstays of an infant in CRISIS due to congeital adrenal hyperplasia

A

hydrocortisone IV or IM (lifesaving)

fluids/glucose

management of hyperkalemia

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18
Q

what is the purpose of mandatory newboen screening

A

the detect potentially fatal or diabling conditions in the newborn before they develop a serious illness

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19
Q

what 3 adrenal gland defects are responsible for primary adrenal insufficiency (addisons disease)

A

adrenal dysfunction/destruction- most common (autoimmune)
adrenal dygenesis (x-linked congential adrenal HYPERplasia)
impaired steroidogensis

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20
Q

primary symptoms of primary adrenal insufficiency

A

all: fatigue, reduced stamina, weakness, anorexia, weight loss, skin hyperpigmentation

some: abdominal pain, MSK pain, psychiatric symptoms, salt cravings, low blood pressure, vomiting

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21
Q

what are the labs in a patient with adrenal insufficiency

wbc:
serum glucose:
serum sodium:
serum postassium:

A

wbc: low- neutropenia
serum glucose: low (low cortisol)
serum sodium: low (low aldosterone)
serum postassium: high(low aldosterone)

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22
Q

in primary adnreal insufficiency also known as _ _ there is _ 8 AM plasma cortisol accompanied simultaneously by signifigant elevation of plasma _

A

addisons disease

low

ACTH

23
Q

what are the symptoms of acute adrenal crisis

A

dehyration, dissiness, rapid heart rate, confusion, fever, headache, abdominal pain

24
Q

what are the lab findings for acute adrenal crisis

cortisol
blood sugar
serum sodium
serum potassium
ph
inadqeuate bump in _ level with a ACTH stimulation test

A

cortisol: low
blood sugar: low
serum sodium: low
serum potassium : high
ph: metabolic acidosis
inadqeuate bump in CORTISOL level with a ACTH stimulation test

25
how do you treat acute adrenal crisis
hydrocortisone (critical) IV/glucose fludrocortisone after hydrocortisone treat hyperkalemia
26
lower than normal serum cortisole would typically result in _ serum ACTH if everything was working normally
increased/high
27
a lack of pituitary secretion of ACTH in response to a low serum cortisol indicated?
that the problem is higher than the adrenal gland itself: pituitary tumor, damage?
28
low serum ACTH in the setting of low serum CORTISOL is consistent with?
secondary adrenal insufficiency
29
signs of cushing syndrome
increased cortisol obesity, truncal weight gain moon face buffalo hump hirsutism thirst.polyuria hypertension dark purple striae mental symptoms impaired wound healing suceptibility to opportunisitc infections
30
elevated midnight cortisol levels are indicative of?
cushing syndrome
31
what is the best screening test for cushing syndrome
dexmathasone stimulation test
32
dexmethasone should suppress _ from the anterior pituitary
ACTH
33
explain the dexmethasone test
1. low dose dexmathasone is given at night 2. serum cortisol levels are drawn in the morning 3. if serum cortisol is below a certain level then you can exclude cushing syndrome 4. you compaire cortisol levels with ACTH levels before dexamathasone was given
34
is acth is low, and cortisol is not suppressed by high or low doses what is the disease
primary hypercortilism meaning that the problem is in the adrenal gland
35
if ACTH is super elevated and cortisol is not suppresed by high or low doses of dexamethasone then this means
there is ectopic acth
36
if ACTH is normal or midly elevated and cortisol is not suppressed by low but is suppresed by low doses what is this outcome
cushing disease (pituitary issue)
37
ectopic ACTH syndrome is often associated with?
small cell carcinoma of the lung
38
why are most patients with primary aldosteronism are hypertensive
excessive aldosterone production increases sodium retention which pulls water with it and increases the blood pressure
39
what are the signs of primary aldosteronism
hypertension, hypokalemia (muscle weakness, polyuria.plydipsia)
40
consider the diagnosis of primary aldosteronism if?
1. treatment resistant hypertension 2. severe hypertension 3. early onset hypertension 4. hypertension with adrenal mass 5. low renin hypertension 6. hypertension with a family history of early onset HTN or CVA 7. 1st degree relative with aldosteroinism
41
primary aldosteronism has what 3 things
hypokalemia metabolic alkalosis low renin hypertension
42
what is conn syndrome
it was a unilateral aldosterone producing adrenal adenoma that caused HTN but not it is just a way to state that someone has primary hyperaldosteronism (from the adrenal gland)- doesnt have to be an adenomatous cause
43
what is the location of a pheochromocytoma and what does it secrete
adrenal medulla secretes catecholamines
44
where is a paraganglioma located and what does ti secrete
outside of the adrenal gland can secrete nothing or secrete catecholamines
45
what are the symptoms of a pheochromocytoma and a paraaganglioma since they present similarily
paroxysmal (sudden) pressure elevated (blood pressure) pounding pain (headache) perspiration panic palpitations pallow (after the spell has subsided) ## Footnote the 7 p's
46
what is the most sensitive test for diagnosing secretory pheochromocytomas and paraganlgiomas
plasma fractionated free metanephrines
47
Von Hippel Linadu- disease type 2 is inherited in a _ (pattern) fashion, 20% of people will develop _ and patients will have _ _ hemangiomas, hemanigioblastomas of the _ and an increased risk for _ _ that transform into renal cell carcinoma
autosomal dominant pheochromocytomas retinal capullary CNS renal cysts
48
how should you treat pheochromocytomas?
alpha blockers first then beta blockers (alpha first because unopposed alpha recetor stimulation can lead to an elevation of blood pressure)
49
adrenal gland incidentalomas are usually found on ?
abdominal CTs, MRI, done for other problems
50
most adrenal gland incidentalomas are _ (benign/malignant)
benign
51
if an adrenal gland is more that _ cm and is not a benign lesion, cyst or has hemorrhage it should be _
4cm ressected
52
if a patient with an adrenal incidentaloma presents then there is required testing for?
cushing syndrome, hyperaldosteroinism, pheochromocytoma testing
53
MEN syndromes are caused by?
gene mutations and tend to run in families