Endocrine Pathology Flashcards

1
Q

Euvolemic hyponatremia with urinary NA+ secretion

Urine osmolality> Blood osmolality

A

SIADH

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2
Q

What happens to Aldosterone and ANP in SIADH

A

Low Aldosterone
High ANP

SIADH increases blood volume which causes the atrial to secrete ANP to lower blood volume and lowers aldosterone secretion which would also increase blood volume.

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3
Q

Rapid correction of SIADH induced hyponatremia can cause

A

Osmotic Demyelination Syndrome

locked in

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4
Q

SIADH can be caused by what malignancy

A

SMALL cell lung Carcinoma

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5
Q

What drugs can caused SIADH

A

Carbamazepine
Cyclophosphamide
SSRIs

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6
Q

How to treat SIADH

A
Fluid restriction is 1st line
Salt Tablets
ADH antagonist (–Vaptans & Demeclocycline)
IV fluids (slowly and if emergent)
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7
Q

What drug causes Nephrogenic DI

high ADH, high blood osmolality, low urine osmolality

A

Lithium

Demeclocycline

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8
Q

A patient with LOW Blood osmolality and LOW urine osmolality probably has

A

Polygenic Polydipsia

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9
Q

Desmopressin elevates urine osmolality after water deprivation test.

A

Central Diabetes Insipidus

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10
Q

Desmopressin minimally increases urine osmolality even after water deprivation test

A

Nephrogenic Diabetes Insipidus

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11
Q

Pituitary tumor, Sheehan syndrome, Blunt head trauma, surgery, encephalopathy can all cause

A

Central Diabetes Insipidus

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12
Q

Ischemic infarct of the pituitary following postpartum bleeding due to hypoperfusion of hypertrophied gland

A

Sheehan syndrome

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13
Q

Presents with failure to lactate post-partum, cold intolerance, ammenorhea

A

Sheehan syndrome

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14
Q

Frontal bossing, large hands and feet, coarse facial features, deep furrows, thick jaw, insulin resistance, +/- lowered labido

A

Acromegaly

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15
Q

Acromegaly increases the risk of _____ cancer

A

Colorectal polyps & cancer

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16
Q

Acromegaly is diagnosed via elevated ____ levels following oral glucose tolerance test

A

IGF-1

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17
Q

Acromegaly is treated with

A

Ocretotide (somatostatin analog)

Pegvisomant (GH receptor anatagonist)

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18
Q

DiGeorge syndrome presents with __ PTH & ___ Phosphate

A

Low PTH

High Ph

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19
Q

Multiple Myeloma presents with ___ Calcium & __ Phosphate

A

High (both)

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20
Q

Elevated Alkphosphate indicates

A

high bone turnover

functioning PTH

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21
Q
How does Chronic Kidney Disease affect levels of:
\_\_\_ Alkphosphate 
\_\_\_ Calcium
\_\_\_ Calciferol (inactive VIt. D)
\_\_\_ pH
A

High (thus PTH is working)
Low
Low (PTH is working, kidneys must be & letting Ca go)
high (PTH and pH always go in the same direction)

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22
Q

High PTH
Low Calcium
*MOST COMMON

A

CKD

Vit. D inactive/deficient (Chron’s, CF, malabsoprtion)

23
Q

Low PTH

High Calcium

A

Cancer

Excess active Vit.D

24
Q

Low PTH

Low Calcium

A
Primary Hypoparathyroidism
(accidentally removed in surgery or autoimmune dest)
25
High PTH | High Calcium
Primary Hyperparathyroidism | Hyperplasia, adenoma/carcinoma
26
presents with episodic hypertension | 200>180
Pheochromacytoma
27
Treatments of Pheochromacytoma FIRST __blocker then __ blocker
alpha (phenoxybenzamine) beta Phenoxybenzamine for Pheochroma A before B
28
Pheochromacytoma can be caused by what 3 mutations
VHL NF-1 MEN2a/b
29
Explain why and alpha blocker needs to be used before a beta blocker in pheochromacytoma?
To prevent HYPERTENSIVE CRISIS Alpha blocker stops Vasoconstriction Beta blockers slow down HR (which would cause vasoconstriction thus HTN)
30
Most common adrenal tumor in children
Neuroblastoma (neural crest cell origin)
31
abdominal mass irrregular firm crosses midline
Neuroblastoma (neural crest cell origin)
32
abdominal mass smooth firm does NOT cross midline (Unilateral)
WIlm's Tumor (Kidney tubular cells)
33
Normotensive baby with an abdominal mass and | jerking limbs, plus non-rhythmic eye movements
Neuroblastoma (neural crest cell origin)
34
Bombesin + NSE+ N-myc amplification Homer Wright- rosettes (small blue round cells in a circle with a pink center)
Neuroblastoma (neural crest cell origin) | *mass may compress spine = DUMBELLS
35
``` Dermatitis (Necrolytic) Diabetes (Hyperglycemia/weight loss) DVT Diarrhea Depression ```
Glucagonoma | *give octreotide
36
Insulinoma is associated with what endocrine disorder
MEN1 | *so is Zollinger-Elison
37
Intestinal ulcers (doudenum/jejunum) Peptic Ulcer Disease diarrhea/steatorrhea Hypertrophies Rugae
Zollinger-Elison | *give octreotide + PPi
38
Asthma/wheezing Diarrhea/ Dermatitis/ Dementia Cutaneous Flushing Murmur (right heart)
Carcinoid syndrome
39
+ Urine 5HIAA
Carcinoid syndrome
40
If a carcinoid tumor is located in the GI tract it will be asymptomatic why?
5HT will go to liver via portal circulation and be inactivated *becomes symptomatic is tumor spreads to the liver
41
Chromogranin A + Synpatophysin + Granular Rosettes
Carcinoid syndrome
42
``` Classic Triad: Hyperpigmentation Hyperkalemia Hypotensive (syncope etc.) Low aldosterone ```
Primary adrenal Insufficiency
43
List 2 causes of chronic Primary adrenal Insufficiency
``` autoimmune destruction (in western world) TB (in developing countries) ```
44
Pituitary apoplexy Sheehan syndrome Pituitary tumor can precipitate secondary
adrenal insufficiency
45
No hyperpigmentation Normal ACTH levels No hyperkalemia normal aldosterone (RAAS okay)
secondary adrenal insufficiency
46
The most common cause of adrenal insufficiency is due to
abrupt withdrawl of glucocorticoid (iatrogenic) *taper patient off of medication
47
Sugar and salt cravings can be suggestive of
Adrenal Insufficiency
48
Adrenal crisis can precipitate
``` hypotensive shock (no aldosterone or cortisol to retain water and vasoconstrict) ```
49
Hypotension Seizures (+/-) Altered mental status Hypotensive shock
Adrenal crisis
50
Elevated ACTH = __ adrenal insufficiency
Primary | * low 11-doxycortisol clinches the diagnosis
51
Low ACTH = __ adrenal insufficiency
secondary/tertiary (glucocorticoid withdrawl)
52
The most common cause of cushing syndrome is due to
``` Iatrogenic (Prednisone) Pituitary adenoma (Organic cause) ```
53
Cushing syndrome can be precipitated by what malignancy
SMALL cell lung cancer