Searchable abstracts of presentations at key conferences in endocrinology

ea0035p839 | Pituitary Clinical (<emphasis role="italic">Generously supported by IPSEN</emphasis>) | ECE2014

Thyrotropinoma: one tumour, two different clinical presentations

Gomez Perez Ana Maria , Selfa Silvia Maraver , Vega Maria Molina , Pareja Isabel Cornejo , Garach Araceli Munoz , Madueno Francisco Tinahones

Thyrotropin-secreting pituitary tumors are <1% of pituitary adenomas. Clinical manifestations are similar to other forms of hyperthyroidism. Most of them are diagnosed as macroadenoma (microadenomas <10%).Case 1: A 48 years old woman with menopause presented 6 years ago, consulting in 2009 for weight loss and palpitations. She had elastic goiter and distal tremor. Blood test: TSH 8.66 μUI/ml (0.2–4.2), FT4 4.7 ng/dl (0.7&#150...

ea0056p894 | Clinical case reports - Thyroid/Others | ECE2018

Postmenopausal virilization with negative imaging

Vega Maria Molina , Doblas Isabel Mancha , Pareja Isabel Cornejo , Garach Araceli Munoz , Selfa Silvia Maraver , Madueno Francisco Tinahones

Introduction: After menopause, an abrupt drop in estrogen levels happens, while ovary androgens secretion declines gradually with aging. This relative hyperandrogenism may lead to the development of hyperandrogenic symptoms. However, the development of marked hirsutism and/or symptoms/signs of virilization, make necessary a detailed study in order to rule out tumorous cause (from adrenal glands or ovaries).Case report: 58 years old woman with progressive...

ea0037ep1169 | Clinical Cases–Pituitary/Adrenal | ECE2015

Oncocytic adrenal cortical adenoma presenting as Cushing's syndrome: an exceptional clinical entity

Vega Maria Molina , Garach Araceli Munoz , Selfa Silvia Maraver , Perez Ana Gomez , Pareja Isabel Cornejo , Perdigones Cristina Diaz , Doblas Isabel Mancha , Madueno Francisco Tinahones

Introduction: Oncocytomas are tumours composed by oncocytes, cells with granular and eosinophilic cytoplasm filled with mitochondria. It is a neoplasm that can arise in several organs (more commonly described in the kidney, salivary gland and thyroid). Oncocytoma arising in the adrenal gland is a rare finding. Most of them are benign and non-functioning and are detected incidentally. However, functional adrenal oncocytomas presenting as Cushing’s syndrome and phaeochromoc...

ea0037ep1207 | Clinical Cases–Pituitary/Adrenal | ECE2015

Cushing's syndrome secondary to aberrant hormone receptors in a patient with macronodular adrenal hyperplasia ACTH-independent

Vega Maria Molina , Medina Jose Antonio Lopez , Garach Araceli Munoz , Pareja Isabel Cornejo , Perdigones Cristina Diaz , Perez Ana Gomez , Madueno Francisco Tinahones

Introduction: Cushing’s syndrome (CS) due to macronodular adrenal hyperplasia ACTH-independent (MAHAI) is rare. Regulation of cortisol secretion by G-protein-coupled receptors (GPCRs) aberrantly expressed is frequently found in MAHAI. Various aberrant receptors have been reported, mostly: GIP, vasopressin, beta-adrenergic, LH/hCG and serotonin.Case report: 61 years old woman. Medical history: type 2 diabetes, hypertension, obesity, dyslipidaemia and...

ea0056p490 | Diabetes therapy | ECE2018

Experience in clinical practice with new long-acting insulins in type 2 diabetes (T2D)

Vega Maria Molina , Garach Araceli Munoz , Fuentes Miguel Damas , Garcia Carmen Hernandez , Perdigones Cristina Diaz , Pareja Isabel Cornejo , Madueno Francisco Tinahones

Introduction: New long-acting insulin analogues (insulin degludec –ID- and insulin glargine 300 U/ml –IG300-) have proved, in clinical trials, that improve metabolic control with lower hypoglycemia rate in T2D.Objective: To assess characteristics of T2D patients who were given ID and IG300 and to evaluate their effect on metabolic control, weight and insulin dose.Material and methods: We studied T2D patients whose treatme...