Searchable abstracts of presentations at key conferences in endocrinology

ea0090ep794 | Pituitary and Neuroendocrinology | ECE2023

MAFLD prevalence in a cohort of patients with Cushing’s disease

Remon Pablo , Gutierrez Ana Pinar , Moreno Eva Venegas , Dios-Fuentes Elena , Gonzales David Cano , Romero-Gomez Manuel , Soto-Moreno Alfonso

Objectives: To describe the prevalence of liver steatosis in a cohort of patients with Cushing’s disease.Methods: Cross-sectional descriptive study. We included 59 patients with Cushing’s disease from our cohort of patients who underwent a Fibroscan to analyze the degree of hepatic steatosis (CAP measured in dB/m) and liver fibrosis (fibrosis measured in kPa). Biochemical algorithms of liver steatosis and fibrosis were assessed.<p class="ab...

ea0063p709 | Pituitary and Neuroendocrinology 2 | ECE2019

Protein expression of convertases involved in POMC processing in silent and functioning corticotroph tumors

Cano David , Garcia-Martinez Araceli , Flores Alvaro , Gil Joan , Puig-Domingo Manel , Webb Susan M , Soto Alfonso , Pico Antonio

Introduction: Previous results of our group, presented in the ECE last year, showed a lower gene expression of proconvertase PC1/3, involved in the processing of POMC, in silent corticotroph tumors (sCT) than in functioning ones (fCT), overall and in microadenomas. The aim of the present study was to quantify the protein expression of convertases involved in the processing of POMC (PC1/3) and in the degradation of ACTH (PC2, CPE and PAM) in a series of CT.</p...

ea0056gp139 | Neuroendocrinology | ECE2018

Why don’t corticotroph tumours always produce Cushing disease?

Garcia-Martinez Araceli , Cano David , Gil Joan , Fajardo Carmen , Camara Rosa , Lamas Cristina , Soto Alfonso , Puig Manel , Webb Susan M

Introduction: Silent corticotroph tumours (SCT) are a pituitary tumours (PT) subtype of corticotroph lineage that do not clinically express Cushing disease. Inmunohistochemical (IHC) studies reveal no differences between SCT and functioning corticotroph tumours with Cushing Syndrome (FCT). However, the silencing mechanisms of this type of tumours are not fully understood.Aim: In an important series of SCT, to sequence the POMC gene and quantify ...

ea0081ep303 | Diabetes, Obesity, Metabolism and Nutrition | ECE2022

Prevalence of sarcopenia with different DXA indices in a population with high-risk obesity

Gonzalez Arnaiz Elena , Gonzalez Roza Lucia , Ramos Bachiller Beatriz , Pintor de la Maza Begona , Barajas-Galindo David , Cano Rodriguez Isidoro , Ballesteros-Pomar Maria

Background: Sarcopenic obesity(SO) is an entity characterized by excess fat mass(FM) and low muscle mass (LMM) and function. Excess FM itself can lead to loss of muscle mass and function at any age. The combination of obesity and sarcopenia is a proven risk factor for frailty, comorbidities and mortality. New diagnostic criteria have been developed for this entity.Aims: To assess the prevalence and severity of SO with different indices by DXA, in a group...

ea0063p39 | Adrenal and Neuroendocrine Tumours 1 | ECE2019

A novel CYP11B1 mutation presenting as a classical congenital adrenal hyperplasia due to 11beta-hydroxylase deficiency

Mazarico Isabel , Gimenez-Palop Olga , Albert Lara , Florencia Luchtenberg , Casamitjana Laia , Capel Ismael , Subias David , Cano Albert , Guitart Miriam , Caixas Assumpta , Rigla Mercedes

Background: Congenital adrenal hyperplasia (CAH) is a rare autosomal recessive disorder, of which 21-hydroxylase deficiency (21OHD) is the most frequent form. 11 beta-hydroxylase deficiency (11bOHD) is the second most common type of CAH. This pathology results from inactivating mutations in CYP11B1 gene.Case presentation: We describe a case of a 48-year-old woman with 11bOHD, presented with hypokalemia hypertension, early adrenarche and mild vir...

ea0063p1087 | Pituitary and Neuroendocrinology 3 | ECE2019

Surgical outcomes in cushing disease: Endoscopic transsphenoidal pituitary surgery

Remon-Ruiz Pablo , Dios-Fuentes Elena , Venegas Eva , Cozar-Duenas Miriam , Kaen Ariel , Cardenas Eugenio , Gonzalez Natividad , Martin Ignacio , Roldan Florinda , Fajardo Elena , Cano David , Soto-Moreno Alfonso

Introduction: Endoscopic transsphenoidal pituitary surgery has become the first line method for removal pituitary tumours. A new way to see the surgical field and the cooperation of two neurosurgeons has supposed a revolution in the area.Objetives: Analyse surgical outcomes and complications of a cohort of patients from a single center who underwent ETPS for Cushing disease.Methods: Descriptive prospective-retrospective study inclu...

ea0063p1091 | Pituitary and Neuroendocrinology 3 | ECE2019

Surgical outcomes in acromegaly disease: endoscopic transsphenoidal pituitary surgery

Cozar Miriam , Remon-Ruiz Pablo , Dios-Fuentes Elena , Cozar Miriam , Kaen Ariel , Cardenas Eugenio , Gonzalez Natividad , Martin Ignacio , Roldan Florinda , Fajardo Elena , Cano David , Soto-Moreno Alfonso

Introduction: Endoscopic transsphenoidal pituitary surgery has become the first line method for removal pituitary tumours. A new way to see the surgical field and the cooperation of two neurosurgeons has supposed a revolution in the area.Objetives: Analyse surgical outcomes and complications of a cohort of patients from a single center who underwent ETPS for GH secreting pituitary tumours.Methods: Descriptive prospective-retrospect...

ea0056p756 | Neuroendocrinology | ECE2018

Pituitary abscesses diagnosis and therapeutic approach in a reference unit

Cozar Miriam , Venegas Eva , Dios Elena , Cano David , Madrazo Ainara , Remon Pablo , Jimenez Enrique , Roldan Florinda , Cardenas Eugenio , Kaen Ariel , Soto Alfonso

Introduction: Pituitary abscess (PA) is a rare condition, representing less than 1% of pituitary lessions. Only around 200 cases have been reported in the scientific literature. Preoperative diagnosis is often challenging due to nonspecific clinical and radiological manifestations.Materials and methods: Retrospective descriptive cohort study. We analyze demographic and clinical variables, hormonal involvement, recurrence, type of surgery and antibiotic t...

ea0056p768 | Neuroendocrinology | ECE2018

ACTH-secreting pituitary adenomas surgical outcomes and complications in Endoscopic transsphenoidal pituitary surgery (ETPS)

Remon-Ruiz Pablo , Dios-Fuentes Elena , Venegas Eva , Kaen Ariel , Cardenas Eugenio , Garcia Natividad , Roldan Florinda , Fajardo Elena , Cano David , Soto Alfonso

Methods: Descriptive retrospective study among patients who underwent ETPS for ACTH-secreting pituitary adenomas performed by the same surgical team from January/2013 to January/2017.Results: 27 ACTH-secreting pituitary adenomas operated via ETPS. 20 (74.1%) were women, median age at surgery was 43.25 [29.65–61.59] years and median follow-up was 3.13 [1.6–6.69] years. Presurgically, 25 (92.59%) patients recieved drugs for control cortisol hyper...

ea0056p769 | Neuroendocrinology | ECE2018

Clinical outcomes and complications in Endoscopic transsphenoidal pituitary surgery (ETPS) for Non-functioning pituitary adenomas

Remon-Ruiz Pablo , Dios Elena , Venegas Eva , Cardenas Eugenio , Kaen Ariel , Garcia Natividad , Roldan Florinda , Fajardo Elena , Cano David , Soto Alfonso

Methods: We conducted a retrospective descriptive study including 67 patients with non-functioning pituitary adenomas surgicaly removed via ETPS beetwen January/2013 to January/2017.Results: Among 67 patients with non-functioning pituitary adenomas surgicaly removed via ETPS 44 (65.67%) were men. 52 (77.61%) patients recieved their first surgery, 14 (20.9%) had been operated one time before and 1 (1.49%) had been operated two times. Every patient reopera...