A 14-year-old girl with a history of type I diabetes mellitus is brought to her pediatrician because of a 2-month history of fatigue, dizziness, and nausea. On physical exam, she is found to have orthostatic hypotension and the pediatrician notes that she has hyperpigmentation of dorsum of her hands and over her knees (Figures 196-1 and 196-2). The pediatrician is concerned about adrenal insufficiency and promptly refers the girl to an endocrinologist. The girl is found to have a low early morning serum cortisol, high serum adrenocorticotropin hormone level, and anti-adrenal antibodies, confirming the diagnosis of primary adrenal insufficiency.
Hyperpigmentation over the dorsal aspect of the hands in a teenager with primary adrenal insufficiency. (Used with permission from Cleveland Clinic Children’s Hospital Photo Files.)
Hyperpigmentation of the skin overlying the knees in the same girl as in Figure 196-1. (Used with permission from Cleveland Clinic Children’s Hospital Photo Files.)
Addison’s disease refers to dysfunction or hypofunction of the adrenal cortex which leads to primary adrenal insufficiency. The adrenal cortex is unable to produce and secrete glucocorticoids (cortisol) and mineralocorticoids (aldosterone), leading to an increase in adrenocorticotropin hormone (ACTH) and systemic effects in children, such as fatigue and gastrointestinal symptoms. Hyperpigmentation of the skin is a distinguishing feature. In children, congenital adrenal hyperplasia is the most common cause of Addison’s disease (see Chapter 197, Congenital Adrenal Hyperplasia). The second most common cause of Addison’s disease worldwide is tuberculosis and other granulomatous disorders. In developed countries, the second most common cause is autoimmune disease, which is the focus of this chapter.1
Primary adrenal insufficiency, adrenocortical hypofunction.
Addison’s disease is rare, with a prevalence of 140 per million.1
Autoimmune Addison’s disease constitutes 15 percent of all cases of primary adrenal insufficiency and usually presents during childhood.
Approximately 1/2 of patients with this disorder also have autoimmune disorders of other endocrine glands. This condition is known as autoimmune polyglandular syndrome (APS) and occurs more often in females (70%).
Etiology and Pathophysiology
Addison’s disease is thought to result from autoimmune attack of the adrenal gland, leading to destruction of the cortical parenchyma.
Autoimmune Addison’s disease is often associated with other autoimmune phenomena, especially polyglandular syndromes.