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Addison's Disease

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Addison's disease

[′ad·ə·sənz di‚zēz]
(medicine)
A primary failure or insufficiency of the adrenal cortex to secrete hormones.
McGraw-Hill Dictionary of Scientific & Technical Terms, 6E, Copyright © 2003 by The McGraw-Hill Companies, Inc.
The following article is from The Great Soviet Encyclopedia (1979). It might be outdated or ideologically biased.

Addison’s Disease

 

(named after the English physician T. Addison, who first described it in 1855), also known as bronzed skin disease. It is caused by a chronic malfunction of the suprarenal cortex of the adrenal glands and is externally characterized by a bronze coloration of the skin. A relatively rare disease, it manifests itself primarily in the 15–to 30–year age group. Addison’s disease is caused by the destruction of the adrenal glands, usually by tuberculosis or more rarely by syphilis, atrophy of the suprarenal cortex, tumor, or amyloidosis. The disease develops gradually.

As a result of the decreased secretion of adrenocortical hormones (mineralcorticoids), the secretion of sodium and chlorides in the urine increases while their amount in the blood decreases, which, together with retention of potassium, leads to the dehydration of the organism. The blood pressure falls. The lowered glucocorticoid content disrupts carbohydrate and protein exchange, causing muscular weakness, adynamia, rapid fatigue, and weight loss. The dark bronze coloring is caused by a special pigment. Hormone treatment is indicated.

REFERENCES

Zefirova, G. S. Addisonova bolezn’. Moscow, 1963. (With bibliography.)
“Bolezni endokrinnoi sistemy.” Edited by V. G. Baranov. (Rukovodstvo po vnutrennim bolezniam, vol. 7.) Leningrad, 1966.
The Great Soviet Encyclopedia, 3rd Edition (1970-1979). © 2010 The Gale Group, Inc. All rights reserved.
References in periodicals archive
to Signs of Addison's disease include a worsening fatigue and muscle weakness, loss of appetite and weight loss are characteristic of the disease.
Jeffcoate, "Eighty-six cases of Addison's disease," Clinical Endocrinology, vol.
Ffion Jones, of Cardiff, died from Addison's disease in December Will Powell
First, we used broad searches to create large pools of citations for each of the nine possible causes (lead, scurvy, dental caries, coffee/tea, tobacco, starvation, botulism, tuberculosis, and Addison's disease) and then ran those against a set of all citations that refer to a black, hard, bleeding and dry oral condition.
Her bloodwork showed hyperkalemia, hypoglycemia, and hypocortisolism, all lab features of Addison's disease, as compared to the hypercortisolism, hyperglycemia, and hypokalemia seen with eating disorders such as AN [12].
Premature mortality in patients with Addison's disease: A population-based study.
Chronic hypoparathyroidism is the first endocrine disease to occur during the time course of PGA I, usually after chronic mucocutaneous candidiasis and before Addison's disease, and can present between three months to 44 years of age (mean, 7.5 yr).
In suspected Addison's disease cases the conventional 250 ug ACTH dose caused maximum cortisol increment both at 30min and 60min from baseline (p< 0.05) whereas with 1 ug ACTH dose significant cortisol increment was observed only at 30 min (p < 0.05) (Table-1).
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