Endocrine Moderate to Severe Hereditary Dog

Addison's Disease

Also known as: Hypoadrenocorticism, Adrenal Insufficiency

Addison's disease (hypoadrenocorticism) results from insufficient production of corticosteroids (cortisol and aldosterone) by the adrenal glands. It is often called 'the great pretender' due to its vague, waxing-and-waning clinical signs that mimic many other diseases. Acute adrenal crisis (Addisonian crisis) is a life-threatening emergency.

Symptoms & Signs

Causes & Risk Factors

Most commonly immune-mediated destruction of the adrenal cortex (primary Addison's). Less common causes include granulomatous disease, metastatic tumors, or iatrogenic (abrupt withdrawal of corticosteroids, mitotane overdose). Secondary Addison's results from pituitary dysfunction.

Diagnosis

ACTH stimulation test (gold standard): both pre- and post-ACTH cortisol levels are low. Electrolyte abnormalities (hyperkalemia, hyponatremia) in classic cases. Baseline cortisol <2 μg/dL is highly suggestive. ECG changes from hyperkalemia.

Treatment

Acute crisis: aggressive IV fluid therapy (0.9% NaCl), dexamethasone. Chronic management: monthly DOCP (desoxycorticosterone pivalate) injections for mineralocorticoid replacement, daily prednisone for glucocorticoid replacement. Stress-dose adjustments.

Prevention

No prevention for immune-mediated form. Gradual tapering of exogenous corticosteroids to prevent iatrogenic form. Careful monitoring during mitotane therapy for Cushing's disease.

Prognosis

Excellent with appropriate lifelong supplementation. Most dogs live normal lifespans with proper management. Requires owner education about stress dosing and emergency recognition.

Affected Breeds (2)

BreedSpeciesSize
Portuguese Water DogDogMedium
West Highland White TerrierDogSmall

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