Peds Adrenal Glands Flashcards

1
Q

What 5 things does angiotensin lead to/do?

A

Gets you to drink, vasoconstriction, aldosterone, increases sympathetic, directly increases reabsorption of sodium and water, ADH.

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2
Q

Big picture, what is our short term stress response?

A

Catecholamines

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3
Q

What is our long term stress response?

A

Glucos and minerals

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4
Q

Is a drop in blood pressure associated with short term dehydration of longer term?

A

Longer term

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5
Q

What is going on with the following labs for CAH?

Sodium, potassium, chloride, bicarb, BUN, creatine and glucose?

A

Down, up, down, down, up, normal, down.

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6
Q

What are the three things you do/give for treatment of CAH?

A

Hydrocortisone, fluids/glucose, and get potassium down (give insulin)

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7
Q

What 3 enzymes are screened for to check for CAH at birth?

A

21 hydroxylase, 17 alpha hydroxylase, and 11 beta hydroxylase

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8
Q

What is the most common cause of primary adrenal insufficiency?

A

Autoimmune

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9
Q

What is the most common infectious cause of primary adrenal insufficiency and what will you see on imaging?

A

TB

Calcification

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10
Q

Why does increased ACTH lead to hyperpigmentation fo the skin?

A

Melano stimulating hormone is a cleaved product of ACTH

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11
Q

6 clinical symptoms in nearly all patients with primary adrenal insufficiency?

A

Fatigue, reduced stamina, weakness, anorexia, weight loss, and skin hyperpigmentation.

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12
Q

4 lab values for primary adrenal insufficiency and what is the confirmatory test?

A

Low sodium, high potassium, low glucose, and a low 8 am cortisol accompanied by elevated ACTH
Cortisol levels not responding to synthetic acth

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13
Q

What serum marker will confirm diagnosis of autoimmune Addison?

A

Antibodies to 21 hydroxylase

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14
Q

What serum marker is required for diagnosis of 21 hydroxylase deficiency?

A

It’s precursor 17 OH progesterone

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15
Q

Why would plasma renin be elevated in primary adrenal insufficiency?

A

Because of the low blood volume

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16
Q

What are the acute adrenal crisis symptoms?

A

Triple H fan

17
Q

What lab values are a dead give away for secondary adrenal insufficiency?

A

Low serum acth with low serum cortisol

18
Q

What imaging technique would you use for ACTH independent Cushing and ACTH dependent?

A

CT of adrenals

MRI of pituitary

19
Q

What is an adrenal incidentaloma?

A

Adrenal nodule discovered incidentally on abdominal CT or MRI

20
Q

What size of mass are we thinking malignancy?

A

Greater than 4 cm

21
Q

If we see a mass, what should all patients be assessed for?

A

Cushings, hyperaldosteronism, and pheo

22
Q

What is conn syndrome?

A

Aldosterone producing adenoma

23
Q

40% of conn syndrome patients have what mutation?

A

Potassium channel

24
Q

3 common clinical symptoms of hyperaldosteronism?

A

HTN and hypokalemia and metabolic alkalosis

25
Q

What do all patients with primary hyperaldosteronism require?

A

CT scan of adrenals to check for adrenal carcinoma

26
Q

What is a paraganglioma and what is the difference between it and conventional pheochromocytoma?

A

Para is an extra adrenal pheo.

Only secretes norepi.

27
Q

What syndrome does he want us to know associated with pheo and what is the inheritance pattern?

A

VHL type 2

Autosomal dominant

28
Q

What is the single most sensitive test for secretory pheo and paras?

A

Plasma fractionated free metanephrines

29
Q

First line treatment of choice for pheo?

A

Alpha blockers

30
Q

What is the inheritance patterns for men syndromes?

A

Autosomal dominant