Nieman Lynnette K
Diabetes, Endocrine and Obesity Branch, The National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), National Institutes of Health, Bethesda, MD, USA.
Endocrinol Metab (Seoul). 2018 Jun;33(2):139-146. doi: 10.3803/EnM.2018.33.2.139.
Cushing's syndrome, a potentially lethal disorder characterized by endogenous hypercortisolism, may be difficult to recognize, especially when it is mild and the presenting features are common in the general population. However, there is a need to identify the condition at an early stage, as it tends to progress, accruing additional morbidity and increasing mortality rates. Once a clinical suspicion is raised, screening tests involve timed measurement of urine, serum or salivary cortisol at baseline or after administration of dexamethasone, 1 mg. Each test has caveats, so that the choice of tests must be individualized for each patient. Once the diagnosis is established, and the cause is determined, surgical resection of abnormal tumor/tissue is the optimal treatment. When this cannot be achieved, medical treatment (or bilateral adrenalectomy) must be used to normalize cortisol production. Recent updates in screening for and treating Cushing's syndrome are reviewed here.
库欣综合征是一种以内源性皮质醇增多为特征的潜在致命性疾病,可能难以识别,尤其是在病情较轻且临床表现为普通人群常见症状时。然而,由于该疾病有进展趋势,会增加额外的发病率和死亡率,因此有必要早期识别。一旦临床产生怀疑,筛查试验包括在基线时或给予1毫克地塞米松后定时测量尿、血清或唾液皮质醇。每项检查都有注意事项,因此必须根据每位患者的情况个体化选择检查。一旦确诊并确定病因,手术切除异常肿瘤/组织是最佳治疗方法。若无法做到这一点,则必须采用药物治疗(或双侧肾上腺切除术)以使皮质醇分泌恢复正常。本文综述了库欣综合征筛查和治疗方面的最新进展。