Cushing's Syndrome in Pediatrics: An Update

被引:66
作者
Lodish, Maya B. [1 ]
Keil, Margaret F. [1 ]
Stratakis, Constantine A. [1 ]
机构
[1] Eunice Kennedy Shriver Natl Inst Child Hlth & Hum, Sect Endocrinol & Genet, NIH, Clin Res Ctr, 10 Ctr Dr,Bldg 10,Room 1E-3330,MSC1103, Bethesda, MD 20892 USA
关键词
Cushing's syndrome; Pituitary tumors; Adrenal cortex; Carney complex; Adrenocortical hyperplasia; Adrenal cancer; CORTICOTROPIN-RELEASING HORMONE; QUALITY-OF-LIFE; ADRENAL INSUFFICIENCY; SALIVARY CORTISOL; ADRENOCORTICOTROPIC HORMONE; BILATERAL ADRENALECTOMY; COAGULATION PROFILE; CLINICAL SIGN; CHILDREN; DIAGNOSIS;
D O I
10.1016/j.ecl.2018.02.008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cushing's syndrome (CS) is a multisystem disorder resulting from the prolonged exposure to excess glucocorticoids. In children, CS most commonly results from the exogenous administration of steroids, and the typical presentation is height deceleration concomitant with weight gain. Endogenous and ectopic causes are rare. CS in children may be associated with distinct germline and somatic mutations. Clinical practice guidelines are available to assist clinicians. Patients should be referred to multidisciplinary centers of excellence with experience in endocrinology and surgery. Early detection and treatment is essential to reduce associated acute and long-term morbidity and potential death.
引用
收藏
页码:451 / +
页数:14
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