Cushing's syndrome in childhood: update on genetics, treatment, and outcomes

被引:13
作者
Lodish, Maya [1 ]
机构
[1] Eunice Kennedy Shriver Natl Inst Child Hlth & Hum, NIH, Sect Endocrinol & Genet, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
childhood; Cushing's disease; medical therapy; pituitary adenoma; radiation; MCCUNE-ALBRIGHT-SYNDROME; MACRONODULAR ADRENAL-HYPERPLASIA; PHOSPHODIESTERASE; 11A4; PDE11A; ENDOCRINE NEOPLASIA TYPE-1; QUALITY-OF-LIFE; PITUITARY-ADENOMAS; BILATERAL ADRENALECTOMY; ADRENOCORTICAL DISEASE; SURGICAL CURE; STEREOTACTIC RADIOSURGERY;
D O I
10.1097/MED.0000000000000127
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of reviewTo provide an update on the genes associated with Cushing's syndrome in children, as well as to familiarize the clinician with recent treatment guidelines and outcome data for children with Cushing's syndrome.Recent findingsThe list of genes associated with Cushing's syndrome continues to grow. In addition, treatment for childhood Cushing's syndrome is evolving. As long-term follow-up data on children becomes available, clinicians need to be aware of the issues that require attention.SummaryKnowledge of the specific genetic causes of Cushing's syndrome has potential implications for treatment, surveillance, and counseling. Advances in surgical technique, radiation modalities, and medical therapies offer the potential for additional treatment options in Cushing's syndrome. Early identification and management of post-treatment morbidities in children treated for Cushing's syndrome is crucial in order to optimize care.
引用
收藏
页码:48 / 54
页数:7
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