Adrenal insufficiency

被引:250
作者
Charmandari, Evangelia [1 ,2 ]
Nicolaides, Nicolas C. [1 ,2 ]
Chrousos, George P. [1 ,2 ]
机构
[1] Univ Athens, Sch Med, Aghia Sophia Childrens Hosp, Div Endocrinol Metab & Diabet,Dept Pediat 1, GR-11527 Athens, Greece
[2] Acad Athens, Biomed Res Fdn, Clin Res Ctr, Div Endocrinol & Metab, Athens, Greece
关键词
CLASSIC 21-HYDROXYLASE DEFICIENCY; CORTICOTROPIN-RELEASING-HORMONE; GENERALIZED GLUCOCORTICOID RESISTANCE; AUTOIMMUNE ADDISONS-DISEASE; PREMATURE OVARIAN FAILURE; G ACTH STIMULATION; QUALITY-OF-LIFE; REPLACEMENT THERAPY; SERUM CORTISOL; DEHYDROEPIANDROSTERONE REPLACEMENT;
D O I
10.1016/S0140-6736(13)61684-0
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Adrenal insufficiency is the clinical manifestation of deficient production or action of glucocorticoids, with or without deficiency also in mineralocorticoids and adrenal androgens. It is a life-threatening disorder that can result from primary adrenal failure or secondary adrenal disease due to impairment of the hypothalamic-pituitary axis. Prompt diagnosis and management are essential. The clinical manifestations of primary adrenal insufficiency result from deficiency of all adrenocortical hormones, but they can also include signs of other concurrent autoimmune conditions. In secondary or tertiary adrenal insufficiency, the clinical picture results from glucocorticoid deficiency only, but manifestations of the primary pathological disorder can also be present. The diagnostic investigation, although well established, can be challenging, especially in patients with secondary or tertiary adrenal insufficiency. We summarise knowledge at this time on the epidemiology, causal mechanisms, pathophysiology, clinical manifestations, diagnosis, and management of this disorder.
引用
收藏
页码:2152 / 2167
页数:16
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