Sos- Adrenal Disorders Flashcards

1
Q

____ glands are crucial for homeostasis

A

endocrine

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

what to be mindful of when removing R kidney

A

IVC (due to short suprarenal vein)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

how adrenal medulla is connected to nervous system

A

innervated by sympathetics and chromaffin cells are stimulated by Ach that is released

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

location of adrenal glands

A

T12-L1 (retroperitoneal too)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

zona glomerulosa regulated by

A

Ang II (RAAS)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

zona fasciculata and reticularis regulated by what

A

CRH and ACTH

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

chromaffin cells of medulla are regulated by what

A

preganglionic sympathetic fibers

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

normally, ____ acts to block inflammation and maintain homeostasis in the body

A

cortisol

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Autonomic NS is fast and overrides _____ in moments of fight or flight

A

endocrine

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

someone with HTN, obesity, advanced diabetes

A

overriding endocrine system to the point where it’s not functioning anymore

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

21-hydroxylase deficiency is the most common cause

A

congenital adrenal hyperplasia (bilateral)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Most common cause of ambiguous genitalia in female newborns

A

congenital adrenal hyperplasia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

75% have salt wasting
Weight loss and dehydration
Adrenal crisis
Elevated 17oh progesterone 48 hrs
Skin pigmentation due to melanocyte stimulating hormone

A

congenital adrenal hyperplasia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

what happens in congenital adrenal hyperplasia when the cause is 21-hydroxylase deficiency

A

decreased cortisol and aldosterone and increased androgens

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Most common
Infants have salt wasting
Precocious puberty
XX virilization

A

21-hydroxylase deficiency

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q
A

21-hydroxylase deficiency

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

why does K+ increase with 21-hydroxylase deficiency

A

b/c aldosterone (and cortisol) are decreased, so that will increase K+ in the serum

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

primary hypothalamic/pituitary disease associated with hypersecretion of ACTH

A

Cushing Disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

____disease results in ____ syndrome and also there can be many causes for the syndrome

A

Cushing

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

most common exogenous cause of Cushing Syndrome

A

(medications)/iatrogenic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

most common endogenous cause of Cushing syndrome

A

pituitary adenoma (ACTH)

22
Q

ACTH dependent endogenous cause of Cushing syndrome that is not pituitary adenoma

A

paraneoplastic

23
Q

main cause of cushing syndrome that is ACTH independent

A

adrenal cortex adenoma

24
Q

Presents with muscle weakness (cortisol metabolizes muscle), HTN, osteoporosis, immune suppression, moon facies truncal obesity and back fat accumulation

A

Cortisol Syndrome

25
exogenous corticosteroids causing Cushing syndrome
26
primary adrenal adenoma causing cushing syndrome
27
ACTH secreting pituitary adenoma causing Cushing syndrome
28
Paraneoplastic ACTH secretion causing Cushing syndrome
29
most common form of Cushing syndrome
Iatrogenic Cushing Syndrome
30
used to treat autoimmune and inflammatory diseases and causes iatrogenic cushing syndrome
glucocorticoids
31
Pituitary ACTH adenoma causing Cushing's Syndrome
32
Secretion of ectopic ACTH by non-pituitary tumors accounts for 10% of cases of Cushing Syndrome
ectopic paraneoplastic cushing syndrome
33
Associated neoplasms: Small cell carcinoma of the lung Neuroendocrine tumors Medullary carcinoma of the thyroid
paraneoplastic cushing syndrome
34
adrenal cushing syndrome caused by cortical adenoma
35
well circumscribed, cortical, yellow in color
Adrenal adenoma
36
decreased production of cortisol and aldosterone; rare Develops slowly and when the patient has a stress (illness or trauma), symptoms worsen
Addison's disease
37
adrenal insufficiency that worsens due to stress (illness or trauma)
Addison's disease
38
Symptoms: Hypoglycemia, hypotension, fatigue Abdominal pain, nausea, diarrhea and vomiting Salt craving Muscle and joint pain Weight loss Can progress to a crisis state
Addison's Disease
39
Young (30-50) Not diagnosed at birth Stress to body, and then it appears Adrenal glands fail and the individuals cant cope with it and cant make cortisol or aldosterone (electrolytes out of whack)
Adrenal Crisis
40
Clinical presentation: Unexplained hypoglycemia and fever Dehydration, hypotension or shock out of proportion to current illness Abdominal pain, nausea and vomiting with a history of weight loss Hyponatremia, hyperkalemia, hypercalcemia
Adrenal Crisis
41
way too much aldosterone treatment resistant HTN affects kidneys, heart, blood vessels
Conn's disease (primary aldosteronism)
42
2 adrenal medullary tumors
neuroblastoma pheochromocytoma
43
Racoon eyes (cancer metastasized to behind the eyes) + mass in abdomen
neuroblastoma of adrenal medulla
44
Catch before 2 years-----80% survival neural crest derived increased levels of urinary catecholamines
Neuroblastoma
45
Homer-Wright rosettes IHC + for NSE, synaptophysin, chromogranin
Neuroblastoma
46
arises from adrenal medulla or sympathetic chain ganglia
Neuroblastoma
47
Zellballen pattern (nests or balls of cells surrounded by connective tissue)
Pheochromocytoma
48
Rule of 10’s 10% malignant, bilateral, extra-adrenal, calcify, in kids
pheochromocytoma
49
IHC+ for NSE, synaptophysin, and chromogranin Most common tumor in adults, but rare
pheochromocytoma
50
HTN that doesn’t respond to HTN meds Mahogany brown (cortex still functioning) but medulla growing
pheochromocytoma
51
produces large amount of epinephrine
pheochromocytoma
52
Episodic hyperadrenergic symptoms, the 5 P’s: Pressure, increased BP Palpitations, heart tachycardia Pain, headaches Perspiration Pallor
Pheochromocytoma