Addison's disease overview: Difference between revisions
Aditya Ganti (talk | contribs) |
Aditya Ganti (talk | contribs) No edit summary |
||
| Line 13: | Line 13: | ||
==Overview== | ==Overview== | ||
Addison disease develops as a result of bilateral adrenal cortex destruction. Both cortisol and aldosterone production are reduced. Autoimmune destruction of the adrenal glands is the most common cause in the western world, but infections such as tuberculosis, hemorrhage, adrenal vein thrombosis, and carcinoma are also known to significant causes. Tuberculosis remains the most common cause worldwide of Addison disease. The onset of Addison disease is often gradual, and symptoms of the disease can be difficult to recognize. It may go undetected until an illness or other stress precipitates adrenal crisis. Treatment should not be withheld to confirm diagnosis. Treatment should be the priority, as the disease is fatal if it remains untreated. Diagnosis is made with rapid, high-dose adrenocorticotropic hormone (ACTH) stimulation testing. If the patient is hypovolemic, dexamethasone and intravenous normal saline should be given before stimulation testing is performed. | Addison disease develops as a result of bilateral [[adrenal cortex]] destruction. Both [[cortisol]] and [[aldosterone]] production are reduced. [[Autoimmune disease|Autoimmune]] destruction of the adrenal glands is the most common cause in the western world, but infections such as [[tuberculosis]], [[hemorrhage]], adrenal vein thrombosis, and carcinoma are also known to significant causes. [[Tuberculosis]] remains the most common cause worldwide of Addison disease. The onset of Addison disease is often gradual, and symptoms of the disease can be difficult to recognize. It may go undetected until an illness or other stress precipitates [[adrenal crisis]]. Treatment should not be withheld to confirm diagnosis. Treatment should be the priority, as the disease is fatal if it remains untreated. Diagnosis is made with rapid, high-dose adrenocorticotropic hormone (ACTH) stimulation testing. If the patient is [[hypovolemic]], [[dexamethasone]] and intravenous normal saline should be given before stimulation testing is performed. The main stay of therapy is with a combination of [[glucocorticoids]] and [[mineralocorticoids]]. [[Glucocorticoid]] doses needs to be doubled when patients have an episode of minor [[fever]], [[infection]], minor trauma, or minor physical stress. Intravenous stress-dose corticosteroids are needed for surgery requiring general anesthesia and for major trauma. | ||
==Historical Perspective== | ==Historical Perspective== | ||
Revision as of 01:48, 15 August 2017
| Title |
| https://https://www.youtube.com/watch?v=V6XcBp8EV7Q%7C350}} |
|
Addison's disease Microchapters |
|
Diagnosis |
|---|
|
Treatment |
|
Case Studies |
|
Addison's disease overview On the Web |
|
American Roentgen Ray Society Images of Addison's disease overview |
|
Risk calculators and risk factors for Addison's disease overview |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Addison disease develops as a result of bilateral adrenal cortex destruction. Both cortisol and aldosterone production are reduced. Autoimmune destruction of the adrenal glands is the most common cause in the western world, but infections such as tuberculosis, hemorrhage, adrenal vein thrombosis, and carcinoma are also known to significant causes. Tuberculosis remains the most common cause worldwide of Addison disease. The onset of Addison disease is often gradual, and symptoms of the disease can be difficult to recognize. It may go undetected until an illness or other stress precipitates adrenal crisis. Treatment should not be withheld to confirm diagnosis. Treatment should be the priority, as the disease is fatal if it remains untreated. Diagnosis is made with rapid, high-dose adrenocorticotropic hormone (ACTH) stimulation testing. If the patient is hypovolemic, dexamethasone and intravenous normal saline should be given before stimulation testing is performed. The main stay of therapy is with a combination of glucocorticoids and mineralocorticoids. Glucocorticoid doses needs to be doubled when patients have an episode of minor fever, infection, minor trauma, or minor physical stress. Intravenous stress-dose corticosteroids are needed for surgery requiring general anesthesia and for major trauma.
Historical Perspective
The condition is named after Dr. Thomas Addison, the British physician who first described the condition in his 1855 On the Constitutional and Local Effects of Disease of the Suprarenal Capsules.[1] The adjective "Addisonian" is used for features of the condition, as well as for patients with Addison's disease.[2]
Diagnosis
Ultrasound
Abdominal ultrasound is typically normal in Addison's disease except for the small size of adrenal glands.
Treatment
Surgery
Surgeries may require significant adjustments to medication regimens prior to, during, and following any surgical procedure. The best preparation for any surgery, regardless of how minor or routine it may be, is to speak to one's primary care physician about the procedure and medication implications well in advance of the surgery.
References
- ↑ Thomas Addison. On The Constitutional And Local Effects Of Disease Of The Supra-Renal Capsules (HTML reprint). London: Samuel Highley.
- ↑ Ten S, New M, Maclaren N (2001). "Clinical review 130: Addison's disease 2001". J. Clin. Endocrinol. Metab. 86 (7): 2909–22. PMID 11443143.