Searchable abstracts of presentations at key conferences in endocrinology

ea0041ep55 | Adrenal cortex (to include Cushing's) | ECE2016

Outcome with surgical treatment in subclinical hypercortisolism

Moreno Cristina , Paja Miguel , Zabalegui Alba , Dublang Maddalen , Etxeberria Eider , Oleaga Amelia , Teresa Gutierrez M

Introduction: Subclinical hypercortisolism (SH), a condition of biochemical cortisol excess without the classical signs or symptoms of overt hypercortisolism, is thought to be present in the 5–30% of patients with incidentally discovered adrenal mass (adrenal incidentalomas). Some evidence suggest that this condition may lead to long-term consequences of cortisol excess, but indication and potential benefits of adrenalectomy in this state are still in doubt. We analyse a ...

ea0035p1115 | Thyroid Cancer | ECE2014

Preoperative TSH value, does it predict the surgical findings in papillary thyroid cancer?

Paja Miguel , Ciriza Maite Perez de , Calles Laura , Etxeberria Eider , Oleaga Amelia , Lizarraga Aitzol

TSH level has been proposed as a thyroid malignancy predictor in nodular thyroid disease. In addition, several clinical studies have reported that higher preoperative serum TSH levels were associated with more advanced stages of differentiated thyroid cancer (DTC) at the time of diagnosis.Methods: We collected retrospectively preoperative serum TSH from patients diagnosed of papillary thyroid cancer (PTC) who had undergone total thyroidectomy during the ...

ea0049ep112 | Clinical case reports - Pituitary/Adrenal | ECE2017

Paraganglioma (PG) and cyanotic congenital heart disease (CCHD): the role of tisular hypoxia

Oleaga Amelia , Goni Fernando , Paja Miguel , Ugarte Estibaliz , Moreno Cristina , Iglesias Natalia , Etxeberria Eider , Calles Laura , Dublang Maddalen , Zabalegui Alba

Introduction: CCHD comprises a number of different congenital heart defects associated with elevated pulmonary artery pressure and pulmonary vascular resistance, resulting in a reversed or bidirectional shunt (Eisenmenger syndrome). These entities develop systemic hypoxia. Pheochromocytoma and paraganglioma (PHEO/PG) are neuroendocrine tumours. Several inheritance genetic alterations have been reported in PHEO/PG syndromes. A pathogenic association between these entities is pr...

ea0049ep1040 | Pituitary - Clinical | ECE2017

Radiological study of clinically non-functioning pituitary macroadenomas: a single institutional experience

Moreno Cristina , Paja Miguel , Lizarraga Aitzol , Etxeberria Eider , Arrizabalaga Cristina , Ugarte Estibaliz , Izuzquiza Ana , Goni Fernando , Iglesias Natalia , Calles Laura

Introduction: When facing with non-functioning pituitary macroadenomas (NFPMA), radiological invasion is determinant to surgical approach, apart from histological biomarkers of pituitary tumor aggressiveness (Ki-67; p53 and mitotic index). Invasive tumors usually need additional surgery and/or radiotherapy. There are no much studies describing epidemiological data on aggressive pituitary tumors in clinical practice. We provide information regarding the radiological findings of...

ea0037ep898 | Thyroid cancer | ECE2015

Cytological variants of papillary thyroid carcinoma: clinical presentations according with the presence of BRAF mutation

Oleaga Amelia , Etxeberria Eider , Calles Laura , Goni Fernando , Fuertes Elena , de Ciriza Maite Perez , Ugalde Aitziber , Paja Miguel

Introduction: BRAF(V600E) mutation has received great attention to improve risk stratification in patients with PTC. Its prognostic value in the different Cytological variants (CytV) of PTC is not well established. The aim of this study was to investigate differences in clinicopathological features according to CytV, among patients harbouring the mutation.Methods: We evaluated 102 patients with pathological diagnosis of PTC. All of them underwent total t...

ea0032p131 | Calcium and Vitamin D metabolism | ECE2013

Predictive factors of postoperative hypoparathyroidism after total thyroidectomy

Paja Miguel , Etxeberria Eider , Calles Laura , Exposito Amaia , Ugarte Estibaliz , Moreno Cristina , Lizarraga Aitzol , Espiga Javier , Oleaga Amelia

Introduction: Hypoparathyroidism (hypoPT) is the most frequent complication after thyroid surgery, usually as transient hypocalcaemia. Permanent parathyroid lesion is less frequent, but it can extend hospital stay and complicate postoperative management. Several preoperative factors predicting the development of hypoPT have been identified, including advanced age, hyperthyroidism, surgical experience and others. We evaluate the role of some potentially predictive factors in ou...

ea0063p89 | Calcium and Bone 1 | ECE2019

Diagnostic and treatment delay in primary hyperparathyroidism (phpt): a pending issue

Paja Miguel , Martinez Adela L , Monzon Andoni , Arrizabalaga Cristina , Zabalegui Alba , Iglesias Natalia C , Calles Laura A , Etxeberria Eider M , Gutierrez Teresa

Background: PHPT is the leading cause of hypercalcemia in outpatients. Its clinical presentation varies from asymptomatic forms to renal or bone complications. The only curative treatment is surgical resection, and delayed diagnosis can lead to serious morbidity.Objective: Identify the presence of PHPT at least one year prior to referral to endocrinology consultation. Secondly, determine whether diagnostic delay leads to increased complications.<p cl...

ea0049ep1217 | Clinical case reports - Thyroid/Others | ECE2017

Simultaneous papillary and medullary thyroid carcinoma in siblings with RET 611 mutation. More than a coincidence?

Paja Miguel , Zabalegui Alba , Dublang Maddalen , Etxeberria Eider , Iglesias Natalia C , Calles Laura A , Arrizabalaga Cristina , Lizarraga Aitzol , Gutierrez M Teresa , Ugalde Aitziber

Germinal mutations of the oncogene RET originate the development of medullary thyroid carcinoma (MTC) in carriers with phenotypic expression depending on the mutated codon and other unknown factors. Simultaneous detection of differentiated thyroid carcinomas is considered a casual phenomenon (collision tumours). We communicate two brothers with double heterozygous mutation of maternal inheritance at codon 611 of RET, TGC to TTT, changing to encode phenylalanine (C611F), with a...

ea0035p1118 | Thyroid Cancer | ECE2014

Clinical and biochemical characteristics of papillary thyroid cancer according to the presence of BRAF (V600E) mutation

Oleaga Amelia , Goni Fernando , Ciriza Miguel Paja1, Maite Perez de , Etxeberria Eider , Calles Laura , Ugarte Estibaliz , Ugalde Aitziber , Elorza J Ramon

Introduction: BRAF (V600E) mutation is the most frequent detected genetic change in papillary thyroid cancer (PTC). Its presence has been related to aggressive clinical and pathological features. Therefore, BRAF mutation has drawn considerable interest as a potential prognostic factor for PTC. The presence of the mutation confers the tumour a disability to uptake RAI, diminishing the therapeutic tools. However if this feature is related to some kind of tumour dedifferentiation...

ea0032p123 | Calcium and Vitamin D metabolism | ECE2013

Early measure of postoperative iPTH and corrected calcium as predictors of future hypoparathyroidism: which, when and why?

Paja Miguel , Moreno Cristina , Ugarte Estibaliz , Oleaga Amelia , Gutierrez Ma Teresa , Izuzquiza Ana J , Etxeberria Eider , Iglesias Natalia C , Lizarraga Aitzol , Martinez-Mate Maria P

Introduction: Intraoperative parathyroid hormone assay (ioPTH) has been validated as a useful tool for predicting postoperative hypocalcaemia (hypoCa) after thyroid surgery and has been proposed as a guide to early discharge from hospital. Its value to predict the risk of future hypoparathyroidism (hypoPT) has not been analyzed in detail. We evaluate this role in our recent surgical series.Description of methods/design: Patients with total thyroidectomy ...