Searchable abstracts of presentations at key conferences in endocrinology

ea0070ep107 | Bone and Calcium | ECE2020

Ectopic parathyroid hormone secretion by a squamous cell carcinoma of the floor of the mouth with poor response to cinacalcet

Bilbao Ismene , Egaña Nerea , Rojo Jorge , Garcia Cristina , Olaizola Izaskun , Agea Leire , Aranburu Maite , Yoldi Alfredo , Goena Miguel

Introduction: Ectopic PTH secretion is rare, to our knowledge, with only 27 cases reported in the literature and 3, ( a tonsil, a lung and a penile) due to squamous cell carcinoma .In the few cases reported to date it appears to be more common in males and in those over the age of 60. The management of the hypercalcemia in this setting is complicated. We are aware of 2 other case reports in which cinacalcet was used in this context, but as in our case, unsuccessfully.<p cl...

ea0056p846 | Pituitary - Clinical | ECE2018

The use of colonoscopic screening in acromegaly in our everyday practice revisited: how compliant with guidelines have we been?

Bilbao Ismene , Egana Nerea , Ciriza Maite Perez de , Olaizola Izaskun , Garcia Cristina , Agea Leire , Aranburu Maite , Yoldi Alfredo , Goena Miguel

Introduction: Although it has been suggested that there is a strong association between acromegaly and premalignant colonic lesions and colon cancer, it seems that in real – life practice the adherence to ACRO colonoscopy guidelines might be lower than expected (as recently shown by M.Parolin et cols).Methods: We retrospectively reviewed the case records of the 54 patients with acromegaly seen in our center since 1994.We analyzed the findings of 27 ...

ea0070ep351 | Pituitary and Neuroendocrinology | ECE2020

Cardiovascular risk factors in acromegaly: comparison between successful surgery with medical treatment

Egaña Zunzunegui Nerea , Bilbao Ismene , García Cristina , Aramburu Maite , Agea Leire , Olaizola Izaskun , Rojo Jorge , Yoldi Alfredo , Goena Miguel

Introduction: Acromegaly is an insidious disease caused by chronic GH and IGF-I hypersecretion associated with increased morbidity and mortality, mostly from cardiovascular complications. The aim of this study is to compare cardiovascular risk factors, between patients with medical treatment vs cured.Materials and methods: This is a retrospective study of 37 acromegalic patients, 21 well controlled with medical treatment (IGF-I within the normal range fo...

ea0090ep1081 | Late Breaking | ECE2023

Cushing Syndrome Due To Acth-Secreting Pheochromocytoma: A Case Report

Ruiz Arnal Laura , Perez Garcia Leire , Agea Diaz Leire , Vega Blanco Maria , Rosario Fuentes Gomez Clara , Gonzalez Gonzalez Sheila , Galarza Montes Aitor , Perez Alonso Octavio , Garaizabal Azkue Leire , Gonzalez Fernandez Mikel

Introduction: The most frequent causes of ACTH-dependent Cushing’s syndrome are of pituitary origin and, less frequently, due to ectopic secretion of bronchial carcinoid, small cell lung cancer, and neuroendocrine tumors; it is rarely caused by an ACTH-producing pheochromocytoma.Methodology: We present a case of a 44-year-old female with a history of poorly controlled type 2 diabetes, hypertension, and long-standing obesity with no genetic predispos...

ea0063p1134 | Reproductive Endocrinology 2 | ECE2019

Hyperandrogenism in postmenopausal women

Zunzunegui Nerea Egana , Garay Ismene Bilbao , Calafell Maite Aramburu , Delgado Cristina Garcia , Agea Leire , Cordeu Maite Perez de Ciriza , Arrieta Alfredo Yoldi , Iregui Izaskun Olaizola , Iglesias Miguel Maria Goena

Introduction: The presentation of new onset hyperandrogenism is extremely rare in postmenopausal women. In premenopausal women, the most common cause of androgen excess is polycystic ovary syndrome. In contrast, when hyperandrogenism develops in postmenopausal women, it is usually associated with other causes, such as ovarian hyperthecosis or an androgen secreting tumor. We describe 5 patients with hyperandrogenism (Table 1). Total Testosterone 0.06–0.86 ng/ml, free testo...

ea0056p147 | Neuroendocrinology | ECE2018

Ectopic cushing’s syndrome: Six cases description

Zunzunegui Nerea Egana , Garay Ismene Bilbao , Cordeu Maite Perez de Ciriza , Iregi Izaskun Olaizola , Calafell Maite Aramburu , Diaz Leire Agea , Delgado Cristina Garcia , Arrieta Alfredo Yoldi , Iglesias Miguel Maria Goena

Introduction: Ectopic Cushing’s syndrome (ECS) is due to ACTH secretion of no pituitary neuroendocrine tumors and represents around 5–10% of all cases of ACTH dependent Cushing’s syndromes.Methods: Six cases of ECS diagnosticated from 2008 to 2017 were studied. Patients’ age ranges from 36 to 69 years (mean 53), four females and two males. Three had pancreatic tumors, two small cell lung carcinomas and one pheocromocytoma. At diagnosi...