Hypothalamus and Pituitary (Correa) Flashcards

1
Q

Which test allows you to make the diagnosis of diabetes insipidus?

A

Fluid deprivation test

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2
Q

Which test allows you to differentiate between central and nephrogenic diabetes insipidus?

A

Desmopressin (ADH) Stimulation test

If central: urine will become more concentrated

If nephrogenic: no change, dilute urine

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3
Q

Central Diabetes insipidus: treatments (3)

A
  • Desmopressin (DDAVP) (synthetic ADH)
  • Carbamazepine
  • Chlorpropamide

oral, or nasal forms

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4
Q

Nephrogenic Diabetes insipidus: Tx

A
  1. Thiazide diuretic (HCTZ)

2. Low salt diet

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5
Q

Name some potential causes of nephrogenic diabetes insipidus

A
  1. Lithium**
  2. Hypercalcemia*
  3. Hypokalemia
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6
Q

What is the clinical hallmark of SIADH?

A

hyponatremia (<135meq) and no evidence of excess water (euvolemic)

Also, increased sodium in the urine

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7
Q

SIADH treatment

A

-restrict fluid (<800ml-1 liter a day)**

if severe: give hypertonic saline and furosemide

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8
Q

SIADH: diagnosis

A
  • low serum osmolarity

- High urine osmolarity

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9
Q

In a patient you are suspicious may have hyperprolactinemia what do you need to rule out?

A
  1. Pregnancy

2. Hypothyroidism (because TRH increase can cause increased prolactin)

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10
Q

What is the best initial test for a patient with galactorrhea and amenorrhea, and infertility?

A

Basal/Fasting prolactin level

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11
Q

Name some drugs that can cause high prolactin?

A
  1. Dopamine antagonists
  2. Methyldopa
  3. Opioids
  4. H2-blockers
  5. Verapamil
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12
Q

In pregnancy which is the preferred dopamine agonist

A

bromocriptine

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13
Q

Discuss the secretion of GH

A
  • pulsatile (undetectable between pulses)

- peak within an hour of start of deep sleep

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14
Q

How is Acromegaly diagnosed?

A

Insulin-like Growth factor is elevated

Confirm dx with oral glucose suppression test (GH will still be elevated)

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15
Q

What diagnostic test is the gold standard in confirming GH deficiency in a child with short stature?

A

GH stimulation test: give insulin and measure serum glucose and serum GH. (normal test: giving insulin should make GH increase)

(do this if you find IGF-1 to be low)

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16
Q

What radiographic modality can be used to help determine is a child has growth failure?

A

Xray of the hand and wrist to compare bone age and chronological age

17
Q

In short stature why measure IGF-1 concentrations?

A
  • stable throughout the day

- reflects the concentration of secreted GH

18
Q

GH Deficiency in children: Tx

A

Somatropin (subcutaneous GH analog)

19
Q

What is the initial test for someone suspected of having acromegaly/gigantism?

A

IGF-1 levels

20
Q

If a patient is found to have high levels of IGF-1, what test should be done?

A

GH suppression test

- Serum GH response to a large dose of glucose
normal: GH should fall below 2ng/dL within 2 hours

21
Q

Acromegaly: common systemic abnormalities

A
  • Large tongue, liver, kidney, thyroid, salivary glands, prostate
  • Electrolytes: Low renin/increased aldosterone, Hypercalciuria, Hypervitamin D
  • Carpal tunnel syndrome (can be initial presentation)*
  • Excessive sweating/oily skin
  • skin tags/colon polyps
  • cardiomyopathy (CHF)
  • Insulin resistance/impaired glucose tolerance
  • DM and hypertriglyceridemia
22
Q

What are 2 common lab abnormalities associated with Acromegaly?

A
  1. Hyperglycemia

2. Hyperprolactinemia

23
Q

What is considered initial therapy for a patient with somatotropinoma aside from transsphenoidal removal of the macroadenoma?

A

1st line: Octreotide (somatostatin analogue) subcutaneous

2nd line: GH receptor antagonist (in the liver)

24
Q

Octreotide ADE

A
  1. Cholecystitis

2. Diarrhea

25
Q

Growth hormone long term management

A
  • Repeat MRI yearly (for the first few years after surgery)
  • Visual field assessment every 6 months
  • Colonoscopy 3-4 year intervals in patients over 50 years
  • Annual heart check
26
Q

Clinical hallmarks of hypopituitarism ?

A

children - abnormal growth

women - menstrual abnormalities

27
Q

Sheehan’s Syndrome

A

-pituitary infarction at the time of delivery–>causing hypopituitarism

28
Q

What is the most common cause of hypopituitarism?

A

pituitary tumor