Canine Pituitary and Adrenal Diseases & Pheochromocytoma Flashcards

1
Q

What is the most common cause of Addison’s disease?

A

primary adrenal faliure due to immune destruction of the adrenal gland

  • secondary pituitary failure is rare
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2
Q

What are 2 causes of iatrogenic Addison’s disease?

A
  1. prolonged use or high doses of Mitotate or Trilostane
  2. prolonged use of glucocorticoids causes adrenal atrophy and an abrupt stop without tapering does not allow time for the adrenal gland to adjust
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3
Q

What is the difference between typical and atypical hypoadrenocorticism?

A

TYPICAL = glucocorticoid AND aldosterone deficient results in hyponatremia and hyperkalemia, usually due to an abnormal adrenal cortex

ATYPICAL = glucocorticoid deficient with normal aldosterone results is normal Na/K, usually due to primary adrenal disease or a decreased in ACTH from the pituitary (aldosterone secreted in response to activation of RAAS, not ACTH)

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4
Q

What is the most common signalment in patients with Addison’s disease? What breeds are predisposed?

A

mean 4.5 y/o female dogs

  • Bearded Collie
  • Standard Poodle
  • Nova Scotia DTR
  • Portuguese Water Dog
  • Great DAne
  • Westies
  • Basset Hounds
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5
Q

What are the most common signs associated with acute onset Addison’s disease?

A
  • bradycardia
  • melena
  • hematochezia

due to shock to GI

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6
Q

What are the most signs associated with gradual onset Addison’s disease?

A
  • GI: anorexia, vomiting, diarrhea
  • lethargic, weak
  • PU/PD —> hyponatremia
  • collapse

(look like dogs with GI disease)

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7
Q

What are the 4 most common things seen on CBC in patients with Addison’s disease?

A
  1. lack of stress leukogram (no cortisol!) - neutrophilia without lymphopenia
  2. lymphocytosis
  3. eosinophilia
  4. mild non-regenerative anemia - GIT bleeding may cause it to become regenerative
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8
Q

What are the 10 most common findings on biochemistry in patients with Addison’s disease? What acid-base abnormality is seen?

A
  1. pre-renal azotemia
  2. hypercalcemia
  3. hyperkalemia
  4. hyperphosphatemia
  5. hypoalbuminemia
  6. hypochloremia
  7. hypocholesterolemia
  8. hypoglycemia - cortisol stimulates gluconeogenesis and glycogenolysis
  9. hyponatremia
  10. increased liver enzymes

metabolic acidosis

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9
Q

What is seen on UA in patients with Addison’s? Why is this significant?

A

< 1.030, minimally concentrated

not concentrated despite pre-renal azotemia (dehydration), due to increased water loss caused by hyponatremia

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10
Q

What imaging can be performed to diagnose Addison’s disease?

A
  • ultrasound: thin adrenals
  • thoracic radiographs: microardia, decreased caudal vena cava size due to hypoperfusion
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11
Q

What are 3 other manifestations of Addison’s disease?

A
  1. severe GI hemorrhage (cortisol required for health and growth of GI mucosa)
  2. megaesophagus
  3. hypoglycemia
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12
Q

What test is used to diagnose Addison’s? What is used for confirmation?

A

baseline cortisol - >2mg/dL = NOT Addison’s; <2mg/dL = COULD be Addison’s

ACTH stim - pre and post <1

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13
Q

What is recommended for Addison’s disease treatment?

A
  • glucocorticoid replacement
  • mineralocorticoid replacement
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14
Q

What 2 options are available for glucocorticoid replacement for Addison’s disease treatment?

A
  1. injectable Dexamethasone - doesn’t cross-react with assay, can be given to crashing patients before diagnosis, may be needed for patients that cannot take pills
  2. Prednisone - can cause false negatives of ACTH stim
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15
Q

What 2 options are available for mineralocorticoid replacement for Addison’s disease treatment?

A
  1. Fludrocortisone (Florinef) - daily, oral
  2. Desoxycortisoterone pivalate (DOCP) - monthly injectable
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16
Q

What is the most life-threatening electrolyte abnormality associated with Addison’s disease? What are 3 treatments?

A

hyperkalemia

  1. fluids - dilution
  2. glucose and regular insulin - shunts K into cells
  3. calcium gluconate - protects heart from conduction issues while K is being decreased
17
Q

What is pheochromocytoma? What does this result in?

A

tumor of the adrenal medulla, resulting in dysregulated catecholamine release (norepinephrine, epinephrine)

  • vasoconstriction, hypertension
  • tachyarrhythmia
  • vasodilation of smooth muscles, collapse
18
Q

What is the most common signalment associated with pheochromocytoma? What are the most common signs?

A

11 y/o with no breed or sex predilection

episodic and variable:

  • weakness, lethargy, anorexia, collapse
  • tachyarrhythmias, tachypnea
  • retinal hemorrhage, pale MM
  • PU/PD
  • muscle tremors, seizures, anxiety, pacing
19
Q

What are the 2 most common signs seen with pheochromocytomas?

A
  1. tachyarrhythmias - typically ventricular
  2. hypertension due to increased HR, contractility, and vasoconstriction - retinal hemorrhage
20
Q

What imaging is used to diagnose pheochromocytoma?

A

AUS and CT - evaluates adrenal gland size and vascular invasion (embolism) of the tumor, as well as metastatic lesions

21
Q

What is the best test to diagnose pheochromocytoma? What is diagnostic?

A

urinary normetanephrine:creatinine ratio

> 4x upper limit —> can overlap in dogs with hyperadrenocorticism or non-adrenal illness, but these instances will not be as high of a result

22
Q

What is the treatment of choice of pheochromocytoma? What can be done before?

A

surgical removal of tumor

  • treat hypertension with Amlodipine
  • Phenoxybenzamine alpha-blocker to stabilize