Searchable abstracts of presentations at key conferences in endocrinology

ea0041ep768 | Neuroendocrinology | ECE2016

Characteristics and management of hospitalized patients with hyponatremia in an endocrinology department

Sanz Revert Pablo , Carlos Ferrer Garcia Juan , Sanchez Juan Carlos , Garcia Blasco Lourdes

Hyponatremia is the electrolyte disorder most commonly encountered in hospitalized patients. The prevalence and characteristics of patients admitted with hyponatremia are analyzed in this study.Description of methods/design: cross sectional study is carried out at the University General Hospital of Valencia, comprising a population of 350,000. 681 of the 30676 patients admitted during the period from January 2014 to December 2015 had hyponatremia include...

ea0056p375 | Diabetes (to include epidemiology, pathophysiology) | ECE2018

HNF-1β maturity-onset diabetes of the young (MODY 5): defining diabetes etiology in a family with different diabetes phenotypes

Silva Carlos , Garcia Elena , Villa Gema , Males David , Romero Juan Carlos , Martinez Guillermo , Leon Miguel

Introduction: HNF-1β maturity-onset diabetes of the young (MODY5) is uncommon, nevertheless accurate diagnosis guides individualized management and informs prognosis in probands and relatives.Objective: To emphasize the importance of the appropriate use of clinical, biochemical and genetic investigations for the correct classification of diabetes etiology.Case-report: A 35-year-old overweight Latin-American male was diagnosed ...

ea0056p379 | Diabetes (to include epidemiology, pathophysiology) | ECE2018

Maternally inherited diabetes and deafness (MIDD): the many faces of the same disease in a Spanish family

Silva Carlos , Garcia Elena , Villa Gema , Martin Alba , Males David , Martinez Guillermo , Leon Miguel

Introduction: Maternally inherited diabetes and deafness (MIDD), is a rare entity. Most commonly, it is related to a point mutation in the mitochondrial DNA (mtDNA) at position 3243 (m.3243A>G) encoding the gene for tRNA. A high index of suspicion is required for the diagnosis due to a wide heterogeneity in its clinical presentation which reflects different levels of mutated mtDNA among mitochondria in a given tissue (heteroplasmy). Thyroid cancer risk has never been speci...

ea0090ep674 | Pituitary and Neuroendocrinology | ECE2023

Tolvaptan in the management of severe hyponatremia associated with acute intermittent porphyria

Gomez Carlos Garcia , Armengod Laura , Abad Ainhoa , Garcia Izquierdo Belen , Guzman Sanz Jorge , Rubio Ramos Miguel , Capristan Diaz Vanesa , Diez Fernandez Natalia , Palacios Nuria

Background: Acute intermittent porphyria (AIP) is an inherited autosomal dominant disorder characterized by hepatic deficiency of hydroxymethylbilane synthase (HMBS)/porphobilinogen deaminase (PBGD), the third enzyme of the heme synthesis pathway. Hyponatremia is one of the main presenting symptoms and it is thought to be related to an inadequate secretion of ADH (SIADH). Since AIP is an uncommon disease, there is little information about how AIP related hyponatremia responds ...

ea0099ep143 | Pituitary and Neuroendocrinology | ECE2024

Pituitary neuroendocrine tumors in elderly patients: clinical and surgical outcomes in a tertiary hospital

Borrego Soriano Ines , Parra Ramirez Paola , Martin Rojas-Marcos Patricia , Perez Lopez Carlos , Garcia Feijoo Pablo , Lisbona Catalan Arturo , Vazquez Perez Paula , Cristina Alvarez Escola Maria

Introduction and aim: The current population is experiencing an increase in life expectancy, with a consequent change in the demographic structure of the society. It is common, therefore, to find elderly patients with pituitary neuroendocrine tumors (PitNET) in our usual clinical practice. Currently, there are no specific recommendations for treatment and data of outcomes in elderly are scarce. The aim of our study was to compare the clinical characteristics and surgical outco...

ea0099ep9 | Reproductive and Developmental Endocrinology | ECE2024

Use of selective adrenal and ovarian venous sampling in postmenopausal women with severe hyperandrogenism: Report of 3 cases

Arsentales Montalva Valeria , Gimenez-Palop Olga , Capel Ismael , Subias David , Romero Ana , Hernandez Alba , Muntean Andreea , Jover Judith , Costa Laura , Perendreu Juan , Garcia Carlos , Rigla Mercedes

Background: Although the majority of cases of hyperandrogenism in postmenopausal women are due to functional causes, the sudden appearance of a severe and rapidly progressive condition, especially if associated with signs of virilization and defeminization, requires always ruling out the existence of an androgen-producing tumor at both the adrenal and ovarian levels. Etiological diagnosis can be difficult because ovarian tumors are not easily demonstrable by imaging.<p cla...

ea0081ep1153 | Thyroid | ECE2022

Role of plasmapheresis in the management of severe amiodarone-induced hyperthyroidism refractory to conventional medical treatment

Garcia Izquierdo Belen , Angulo Macarena Contreras , Grao Laura Armengod , Garcia Gomez Carlos , Garcia Garcia Alvaro , Maroto Azucena Losa , Cabrera Jose Luis Bueno , Serrano Miguel Juan Garcia- Oria , Donoso Encarnacio n , Iglesias Pedro

Introduction: Amiodarone is an antiarrhythmic drug whose high iodine content may influence thyroid function. The first line treatment of amiodarone-induced hyperthyroidism (AIH) is mainly medical. Plasmapheresis has been used in cases of antithyroid intolerance or refractory hyperthyroidism, although clinical experience is poor.Clinical case: We present a case of a patient with structural heart disease and severe AIH refractory to medical treatment who r...