| Literature DB >> 25617921 |
Abstract
The development of molecular biology tools has allowed major advances in the genetic determinism and the pathophysiology of pheochromocytomas and Conn's adenomas. However, the molecular pathophysiology of ACTH-independent Cushing's Syndrome was mostly unknown until recently. In 2014, major new insights concerning the physiopathology of ACTH-independent macronodular adrenal hyperplasias (AIMAH) and the cortisol-secreting adenomas have been published. Elsewhere, the cardiovascular consequences of the subclinical hypercortisolism due to adrenal incidentalomas, was described only in some cross-sectional studies. The natural history of these lesions has been documented in two large follow-up studies. These new data presented during the Endocrine Congress are summarized herein.Entities:
Keywords: ACTH-independent Cushing's syndrome; ARMC5 mutations; Adénomes cortisoliques infracliniques; Bilateral Macronodular Adrenal Hyperplasia (AIMAH); Hyperplasie macronodulaire bilatérale des surrénales; Mutations ARMC5; Mutations PRKACA; PRKACA mutations; Subclinical Cortisol-Secreting Adenomas; Syndrome de Cushing ACTH-indépendant
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Year: 2014 PMID: 25617921 DOI: 10.1016/S0003-4266(14)70025-3
Source DB: PubMed Journal: Ann Endocrinol (Paris) ISSN: 0003-4266 Impact factor: 2.478