Lab 3 & 4 Flashcards

1
Q

Cushing’s disease

A

Hyperadrenocorticism
syn. 1. Hypercortisolemia
2. cushing’s syndrome

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2
Q

Clinical signs of Hyperadrenocorticism

A

Polyuria; polydipsia
polyphagia
panting
abdominal distention
hepatomegaly
muscle weakness
pot bellied appearance

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3
Q

dermatologic signs of Hyperadrenocorticism

A

Symmetric truncal alopecia
Hyperpigmentation
Comedones
Thin skin
poor hair regrowth

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4
Q

Diagnostic process for Hyperadrenocorticism

A
  1. Urinalysis
    2, Chemistry Panel
  2. CBC
  3. Lddst
  4. ACTH stimulation test
  5. Urine-cortisol-to-creatinine ratio
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5
Q

Urinalysis (Hyperadrenocorticism)

A

specific gravity < 1.008
Protenuria may be noted and quantified with urine protein-to-creatinine ratio

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6
Q

Chemistry Panel (Hyperadrenocorticism)

A

increased alkaline phosphatase (ALP) activity

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7
Q

CBC (Hyperadrenocorticism)

A

stress leukogram (neutrophilia, lymphopenia, monocytosis and eosinopenia)

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8
Q

Forms of Hypoadrenocorticism

A
  1. Primary Hypoadrenocorticism
  2. Atypical Hypoadrenocorticism
  3. Secondary Hypoadrenocorticism
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9
Q

Adrenal destruction is purported to spare the glomerulosa layer, resulting in an isolated glucocorticoid deficiency.

A

Atypical Hypoadrenocortcicism

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10
Q

results from immune-mediated destruction of adrenal cortical tissue. the adrenal glands don’t make enough of the hormones cortisol and aldosterone

A

Primary Hypoadrenocorticism

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11
Q

refers to a central (anterior pituitary) deficiency of ACTH, resulting in isolated glucocorticoid inusfficiency

A

Secondary Hypoadrenocorticism

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12
Q

Primary hypoadrenocorticism is reported in what ages in dogs

A

young to middle-aged female dogs

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13
Q

Atypical Hypoadrenocorticism is primary seen in what group

A

Occurs at older ages

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14
Q

Clinical signs of mineralocorticoid insufficiency

A

-Low sodium concentrations
-high potassium concentrations

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15
Q

Glucocorticoid insufficiency

A

Lethargy/weakness
Shaking
Polyuria / Polydipsia
Vomiting / diarrhea
Abdominal pain
Inappetence/ weight loss

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16
Q

Gold standard for diagnosis or all forms of hypoadrenocorticism

A

ACTH stimulation test

17
Q

Treatment for hypoadrenocorticism

A

Aggressive IV isotonic crystalloids
- Monitoring of packed cell volume / total solids, serum electrolytes, and blood glucose on every 6-8 hours until values have normalized and patients is clinically stable

18
Q

What to avoid in emergency setting for Hypoadrenocorticism

A
  • avoid administration of prednisone, prednisolone and cortisone acetate
  • avoid SC admin of DOCP
  • avoid PO admin of any medication