Adrenal insufficiency
Updates to Article Attributes
Body
was changed:
Addison disease also known as adrenal insufficiency refers to inadequate secretion of corticosteroids from partial or complete destruction of adrenal glands.
Pathology
Addison disease has a number of causes:1
- idiopathic autoimmune disorders which is the most common cause (80% of cases) in developed countries1
- granulomatous disease: tuberculosis (is the most common infectious cause in underdeveloped countries), sarcoidosis
- neoplasms: metastases (e.g. lung, ovary, kidney, melanoma), lymphoma, leukemia
- adrenal hemorrhage: shock, sepsis (Waterhouse-Friderichsen syndrome ), coagulation disorders, antiphospholipid syndrome
- systemic fungal infection: histoplasmosis (most common infection in southeastern and south central
USAUnited States)1
The disease course may be either acute, subacute, or chronic 2
- acute: occurs within a few weeks to months and is caused by bilateral adrenal hemorrhage (adrenal apoplexy) or secondary to shock and sepsis or trauma (Addisonian crises)
- subacute disease (adrenalitis): when the disease has been present for less than 2 years
- chronic: secondary to chronic autoimmune disorder or chronic granulomatous infection (tuberculosis), the adrenal glands become atrophic and calcified
Clinical presentation
Depends on the course of the disease
- acute stage: the patient presents with fever, back pain, hypotension, weakness
- chronic stage: progressive lethargy, weakness, cutaneous pigmentation, weight loss
Laboratory data
- chemistry: hyponatremia, hyperkalemia, azotemia, hypercalcemia, hypoglycemia
-
Adrenocorticotrophicadrenocorticotrophic hormone (ACTH) stimulation test: cortisol level fail to fall
Radiographic features
General
- Addison is bilateral disease
- cannot diagnose Addison disease by imaging alone
- CT is the best imaging modality
CT
Imaging features depend on the cause and the course of the disease either acute, subacute or chronic
- acute: bilateral adrenal hematomas are demonstrated.
- subacute (adrenalitis): enlargement of both adrenal glands, with necrotic centers and peripheral enhancing rim
- chronic: both adrenal glands appear small and atrophic associated with calcifications (adrenal calcification) in granulomatous adrenalitis
Treatment and prognosis
- acute: glucocorticoid therapy, volume and electrolytes replacement and correct etiology
- chronic: glucocorticoid and mineralocorticoid replacement
Differential diagnosis
-<li>systemic fungal infection: histoplasmosis (most common infection in southeastern and south central USA)<sup>1</sup>- +<li>systemic fungal infection: histoplasmosis (most common infection in southeastern and south central United States)<sup>1</sup>
-<li>Adrenocorticotrophic hormone (ACTH) stimulation test: cortisol level fail to fall</li>- +<li>adrenocorticotrophic hormone (ACTH) stimulation test: cortisol level fail to fall</li>
-<li>-<strong>CT</strong> is the best imaging modality </li>- +<li>CT is the best imaging modality </li>
-</ul><h4>Treatment</h4><ul>- +</ul><h4>Treatment and prognosis</h4><ul>
-<li><a href="/articles/adrenal-tb">adrenal TB</a></li>- +<li><a href="/articles/adrenal-tb">adrenal tuberculosis</a></li>
Images Changes:
Image 1 CT (C+ portal venous phase) ( update )
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Case 1: secondary to TBtuberculous infection
Image 2 X-ray (Frontal) ( update )
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Case 2: calcified adrenal glands secondary toadrenals from previous tuberculosis