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Addison disease - Oral Mucosal Lesion
See also in: Overview
Other Resources UpToDate PubMed

Addison disease - Oral Mucosal Lesion

See also in: Overview
Contributors: Carl Allen DDS, MSD, Sook-Bin Woo MS, DMD, MMSc
Other Resources UpToDate PubMed

Synopsis

Addison disease is a chronic primary adrenocortical insufficiency resulting from dysfunction of the adrenal glands. This can be due to a variety of causes, which include autoimmune diseases, infections (tuberculosis), and neoplasms (metastatic cancer). The most common associated autoimmune diseases are Type I diabetes mellitus, Hashimoto thyroiditis, and vitiligo. Patients with acquired immunodeficiency syndrome may develop Addison disease due to cytomegalovirus infection. Other less common causes are drugs (antifungals), congenital adrenal hypoplasia, and disorders such as sarcoidosis and amyloidosis. Some cases are idiopathic. Patients with loss-of-function mutations in sphingosine-1-phosphate lyase may have nephrosis with ichthyosis and adrenal insufficiency.

The adrenal insufficiency leads to decreased levels of glucocorticoids (the most common), mineralocorticoids, and adrenal androgens. The disease is characterized by general symptoms of fatigue, weight loss, weakness, vomiting, dizziness, cold intolerance, and muscle aches. Because these symptoms are nonspecific, the diagnosis may go unrecognized until the patient presents with a life-threatening adrenal crisis (severe hypotension and even coma).

The cutaneous manifestation of patients with chronic Addison disease is hyperpigmentation of skin and mucous membranes. Skin pigmentation, which appears as "bronzing" of the skin, is generalized and mainly affects sun-exposed areas. Oral mucosal lesions present as dark brown to black macules and frequently are the first sign of disease. These and the other clinical signs of the disease appear only after 90% of the adrenal gland is nonfunctioning. The hyperpigmentation is due to increased production of melanocyte-stimulating hormone (MSH), which is part of the adrenocorticotrophic hormone (ACTH) molecule; ACTH production in the pituitary increases in response to decreased cortisol production, leading also to an increase in MSH levels and melanosis.

Men and women are equally affected, and although all ages are affected, it is more common between the ages of 30 and 50. Estimated prevalence of the disease is at 120 per million.

Addisonian Crisis:
Acute adrenal failure presents with severe penetrating abdominal pain accompanied by vomiting and diarrhea, low blood pressure, and loss of consciousness. This is a life-threatening emergency that must be managed aggressively.

Codes

ICD10CM:
E27.1 – Primary adrenocortical insufficiency

SNOMEDCT:
363732003 – Addison disease

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Last Updated:03/06/2017
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Addison disease - Oral Mucosal Lesion
See also in: Overview
A medical illustration showing key findings of Addison disease (Common Features) : Abdominal pain, Fatigue, Hyperkalemia, Muscle weakness, Anorexia, Postural hypotension, Na decreased
Clinical image of Addison disease - imageId=2729975. Click to open in gallery.  caption: 'Hyperpigmented patches on the dorsal fingers.'
Hyperpigmented patches on the dorsal fingers.
Copyright © 2024 VisualDx®. All rights reserved.