4.3 Review

Recent Updates on the Diagnosis and Management of Cushing's Syndrome

Journal

ENDOCRINOLOGY AND METABOLISM
Volume 33, Issue 2, Pages 139-146

Publisher

KOREAN ENDOCRINE SOC
DOI: 10.3803/EnM.2018.33.2.139

Keywords

Cushing syndrome; Hydrocortisone; Adrenocorticotropic hormone

Funding

  1. National Institutes of Health

Ask authors/readers for more resources

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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.3
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available