| Literature DB >> 32787757 |
Miomira Ivović1, Ljiljana V Marina1, Antoan S Šojat1, Milina Tančić-Gajić1, Zorana Arizanović1, Aleksandra Kendereški1, Svetlana Vujović1.
Abstract
A growing number of patients with adrenal incidentalomas and subclinical Cushing's syndrome (SCS) led to an increasing number of different guidelines, and diagnostic and treatment recommendations. Excess cortisol secretion in patients with SCS is associated with several comorbidities, such as hypertension, dyslipidemia, type 2 diabetes mellitus, and obesity, which in the long-term increase mortality of these patients. Subtle cortisol secretion affects bone health, quality of life and causes depression, but due to the unapparent clinical features, patients with SCS are often at risk between over and under treatment. This narrative review aimed to summarize the latest recommendations on the approach to the patient with subclinical Cushing's syndrome. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.Entities:
Keywords: Subclinical Cushing's syndrome; adrenal incidentaloma; adrenal tumor; mild autonomous cortisol excess; mild autonomous cortisol secretion; non-functional adrenal incidentaloma; possible autonomous cortisol secretion
Year: 2020 PMID: 32787757 DOI: 10.2174/1381612826666200813134328
Source DB: PubMed Journal: Curr Pharm Des ISSN: 1381-6128 Impact factor: 3.116