Literature DB >> 25617921

[New insights in adrenal Cushing syndrome].

M Haissaguerre1, A Tabarin2.   

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.
Copyright © 2014 Elsevier Masson SAS. All rights reserved.

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


  1 in total

1.  Adrenocortical Challenge Response and Genomic Analyses in Scottish Terriers With Increased Alkaline Phosphate Activity.

Authors:  Kurt L Zimmerman; David L Panciera; Ina Hoeschele; W Edward Monroe; Stephanie Michelle Todd; Stephen R Werre; Tanya LeRoith; Kellie Fecteau; Bathilda B Lake
Journal:  Front Vet Sci       Date:  2018-10-09
  1 in total

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