Abstract Search

ea0049ep76 | Adrenal cortex (to include Cushing's) | ECE2017

Clinical course of patients with adrenal incidentaloma: retrospective analysis of a single center

Serrano Ana Carolina Ruiz , Colet Ana Megia , Cortes Silvia Naf , Ortega Joan Vendrell , Muela Inmaculada Simon , Fraile Esther Solano , Alevras Theodora Michalopoulou

In the adrenal incidentaloma (AI) it is fundamental to determine functionality and benignity. The aim of this study was to evaluated the clinical, radiological and hormonal evolution of AI and compare the frequency of autonomous cortisol secretion (ACS) between American and European Guidelines.Methods: Retrospective evaluation of patients with AI referred to our service in the last 5 years.Results: 140 patients were included, 50.9%...

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ea0056p108 | Clinical case reports - Thyroid/Others | ECE2018

Syndrome carney-stratakis, new mutation report: SDH B: D138Y (c.412>T)

Serrano Ana Ruiz , Ciccia Alessandra Gabillo , Maduena Francisca Martinez , Gonzalez Salome Martinez , Ambros Josep Oriola , Simon-Muela Inmaculada , Ortega Joan Vendrell , Cortes Silvia Naf , Alevras Theodora Michalopoulou , Colet Ana Megia

Introduction: The Carney-Stratakis syndrome (CSS) is an inherited condition caused by germline mutations in succinate dehydrogenase (SDH) subunits B, C or D that predispose to gastric stromal tumors (GIST) and multicentric paragangliomas (PGL). SDH acts as a tumor suppressor gene, and enzyme activity reduction is known to be oncogenic. Since 2002 there has been some scarce reports. We present a new case of CSS associated with a germline unknown significance mutation in exon 4 ...

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Endocrine Abstracts

Clinical course of patients with adrenal incidentaloma: retrospective analysis of a single center

Syndrome carney-stratakis, new mutation report: SDH B: D138Y (c.412>T)

BiosciAbstracts