Searchable abstracts of presentations at key conferences in endocrinology

ea0014p440 | (1) | ECE2007

Thyrotropin-producing pituitary adenoma discovered because of galactorrhea

Herrera M Teresa , Abreu Cristina , Hemmersbach-Miller Marion , Darias Ricardo , Olvera Pilar , Palacios Enrique

Introduction: Thyrotropin-producing adenomas (TSH-omas) constitute about 1% of pituitary adenomas. TSH-omas are a rare cause of hyperthyroidism. In conjunction with biochemical parameters and dynamic endocrine testing, image evaluation of the pituitary gland and sella turcica is mandatory for establishing a correct diagnosis. TSH-omas are usually large tumors and tend to be invasive. Greater amounts of invasion correlate with incomplete surgical removal of the tumor and, thus,...

ea0056p698 | Clinical case reports - Pituitary/Adrenal | ECE2018

Diabetes insipidus as first clinical manifestation of pineal tumor

Gonzalez Cristina Lorenzo , Mesa Elena Marquez , Huerta Yolanda Zambrano , Marquez Maria Pilar Olvera , Arranz Maria Teresa Herrera , Abizanda Enrique Palacio

Introduction: Central diabetes insipidus is a disorder characterized by polyuria and polydipsia due to vasopressin deficiency caused by a lesion at the hypothalamo-hypophyseal axis. Frequently, central diabetes insipidus is wrongly considered idiopathic if not associated with other neurological signs and symptoms. Herein we present the report of a case that illustrates the difficulties in the diagnosis of this condition.Case report: A 17 year-old male wa...

ea0056p945 | Female Reproduction | ECE2018

Current situation of adult patients with Turner syndrome in Tenerife (Spain)Current situation of adult patients with Turner syndrome in Tenerife (Spain)

Mesa Elena Marquez , Garcia Jose Gregorio Oliva , Rodriguez Jose Manuel Rial , Marquez Pilar Olvera , Arranz Maria Teresa Herrera

Introduction/ objectives: Turner syndrome (TS) comprises a group of sex chromosomal abnormalities of heterogeneous clinical presentation. During the infant period, the pediatric endocrinologist coordinates their follow-up and it is important to ensure its continuation during the adult stage. The objective of this study is to know the current clinical situation, occupational, educational, social and medical monitoring of patients affected TS in Tenerife.M...

ea0063p869 | Adrenal and Neuroendocrine Tumours 3 | ECE2019

An unusual case of classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency diagnosed in the adulthood

Gonzalez Cristina Lorenzo , Arranz Maria Teresa Herrera , Marquez Maria Pilar Olvera , Huerta Yolanda Zambrano , Fernandez Javier Garcia , Mesa Elena Marquez , Abizanda Jose Enrique Palacio

Introduction: Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (classic 21-OHD CAH) is the most common form of congenital adrenal hyperplasia, characterized by simple virilizing or salt wasting forms. The saline loss picture develops after birth and it can evolve in a short time to a severe picture of hypotonic dehydration and hypovolemic shock with lethal consequences if not diagnosed and treated. Herein we present an unusual case of classic 21-OHD CAH ...

ea0063p1116 | Pituitary and Neuroendocrinology 3 | ECE2019

Giant cerebral aneurysm a rare cause of hypopituitarism: a case report

Huerta Yolanda Zambrano , Marquez Pilar Olvera , Arranz Maria Teresa Herrera , Gonzalez Cristina Lorenzo , Fernandez Javier Garcia , Izquierdo Marcos Perera , Abizanda Enrique Palacio

Introduction: Hypophysary aneurysms are rare, they account for 1% to 2% of all intracranial aneurysms (1) and can be mistaken for pituitary adenomas, since they can have similar symptoms and even radiological signs especially if it’s an aneurysm completely thrombosed as angiography will show only avascular mass (2).Clinical case: A 84 year old female with past medical history of hypertension, dyslipidemia and depressive disorder, presents to emergen...

ea0049ep862 | Clinical case reports - Pituitary/Adrenal | ECE2017

Esthesioneuroblastoma causing ectopic ACTH Syndrome

Gonzalez Cristina Lorenzo , Melo Estefania Gonzalez , Mesa Elena Marquez , Marquez Pilar Olvera , Arranz Maria Teresa Herrera , Bray Bruno Francisco Garcia , Huerta Yolanda Zambrano , Abizanda Enrique Palacio

Introduction: Esthesioneuroblastoma is an uncommon malignant neoplasm with an average 5-year survival rate of about 45%. Ectopic ACTH syndrome due to esthesioneuroblastoma is extremely rare and there have been very few cases reported.Case report: A 54-year-old woman was admitted to our hospital with symptoms of leg edema and general fatigue of one month’s duration. Physical examination showed moon facies and edema on her lower extremities bilaterall...

ea0049gp240 | Thyroid Cancer & Thyroid Case Reports | ECE2017

Giant goiter with intrathyroid arteriovenous fistula as a cause of severe pulmonary hypertension

Mesa Elena Marquez , Melo Estefania Gonzalez , Gonzalez Cristina Lorenzo , Marquez Pilar Olvera , Garzon Ricardo Darias , Arranz Maria Teresa Herrera , Bray Bruno Francisco Garcia , Huerta Yolanda Zambrano , Abizanda Enrique Palacio

Introduction: Hyperthyroidism has been described as a rare cause of pulmonary hypertension (PH) as well as systemic arteriovenous fistulas. However, we describe a case of pulmonary hypertension secondary to an intrathyroid arteriovenous fistula, not previously described in the literature.Case report: A 56 year old woman followed in our consultations with multinodular goiter and a long standing hyperthyroidism, secondary to Graves Basedow disease with dif...

ea0056gp11 | Acromegaly | ECE2018

Observational, multicentre study to evaluate the effectiveness in routine clinical practice of Lanreotide Autogel 120 mg at extended dosing intervals (>4 weeks) for the treatment of acromegaly: SOMACROL study

Escola Cristina Alvarez , Fajardo Carmen , Marazuela Monica , Carballido Fernando Cordido , Venegas Eva Maria , Velasco Pedro de Pablos , Maroto Gonzalo Piedrola , Marquez Ma del Pilar Olvera , de Paz Isabel Pavon , Carvalho Davide , Romero Carme , De la Cruz Guillermo , Bernabeu Ignacio

Background: Acromegaly is usually caused by a benign pituitary tumour, with increased production of growth hormone (GH) and insulin-like growth factor 1 (IGF-1). Treatment options include surgery, followed by pharmacological treatment with dopamine agonists, somatostatin analogues, GH receptor antagonists or radiotherapy. Treatment optimization is important to decrease the burden of this often-chronic disease on the patient.Objectives: To evaluate the ef...

ea0081p166 | Pituitary and Neuroendocrinology | ECE2022

Pasireotide imaging study: magnetic resonance imaging as a predictor of therapeutic response in acromegaly

Ruiz Sabina , Venegas Moreno Eva , Gil Joan , CAMARA ROSA , Biagetti Betina , Angeles Galvez Moreno Maria , Maraver Silvia , Gonzalez-Molero Inmaculada , Pico-Alfonso Antonio , Abellan Galiana Pablo , trincado pablo , Teresa Herrera Arranz Maria , Olvera Pilar , Xifra Villarroya Gemma , Bernabeu Ignacio , Azriel Mira Sharona , Garcia-GarciA-Doncel Lourdes , Jorda Mireia , Valassi Elena , Puig-Domingo Manel

Background: T2-weighted magnetic resonance imaging (MRI) signal has been recently linked with a better tumor response to pasireotide treatment in patients with acromegaly (ACRO). Our aim was to evaluate the prevalence of this radiological feature and its association to therapeutic outcomes in a large cohort of ACRO patients treated with pasireotide.Methods: A retrospective multicentre study was performed in 15 Spanish tertiary university hospitals includ...